Samacheer Kalvi 12th Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers

Tamilnadu State Board Solutions for Class 12th Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Questions and Answers will help you to improve the complete subject knowledge. Every student must look at the single concept included in Samacheer Kalvi 12th Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Book Solutions Answers Guide Solutions PDF. All the concepts are explained clearly with examples and pictures.

Students can easily avoid the struggle to get the best book for Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Book Solutions Answers Guide learning. You have to go through Chapterwise Samacheer Kalvi Class 12th Textbook Solutions for Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Book Solutions for better practice.

Tamilnadu Samacheer Kalvi 12th Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers

Students who wish to have the strong basics of Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers can use Tamilnadu State Board Class 12th Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Questions and Answers Guide pdf. Enhance your knowledge by referring to the Samacheer Kalvi Solutions pdf. We provided a free pdf of Tamilnadu State Board Class 12th Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Book Solutions Answers Guide material and textbook for students. Check it out now and start preparing for the exam immediately. Score maximum marks in the exam by referring to Samacheer Kalvi Class 12th Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Book Solutions Answers Guide Solutions Pdf.

Samacheer Kalvi 12th Chemistry Chapter 11 Hydroxy Compounds and Ethers Textual Evaluation Solved

Samacheer Kalvi 12th Chemistry Hydroxy Compounds and Ethers Multiple Choice Questions

12th Chemistry Chapter 11 Book Back Answers Question 1.
An alcohol (x) gives blue colour in victormayer’s test and 3.7g of X when treated with metallic sodium liberates 560 mL of hydrogen at 273 K and 1 atm pressure what will be the possible structure of X?
(a) CH₃ CH (OH) CH₂CH₃
(b) CH₃ – CH(OH) – CH₃
(c) CH₃ – C (OH) (CH₃)₂
(d) CH₃ – CH₂ – CH (OH) – CH₂ – CH₃
Answer:
(a) CH₃ CH (OH) CH₂CH₃
Hint:
2R – OH + Na → 2RONa + 2H₂ ↑ 2 moles of alcohol gives 1 mole of H₂ which occupies
22.4L at 273K and 1 atm
number of moles of alcohol = \(\frac{2 \text { moles of } \mathrm{R}-\mathrm{OH}}{22.4 \mathrm{L} \text { of } \mathrm{H}_{2}}\) x 560 mL = 0.05 moles
number of moles = \(\frac{\text { mass }}{\text { molar mass }}\)
= molar mass = \(\frac{3.7}{0.05}\) = 74 g mol^-1
General formula for
R – OH C_n H_2n+1 – OH
n(12) + (2n+1) (1) + 16 +1 = 74
14n = 74 – 18
14n = 56
n = \(\frac { 56 }{ 4 }\) = 4
The 2° alcohol which contains 4 carbon is CH_n CH(OH)CH₂ CH₃

Hydroxy Compounds And Ethers Pdf Question 2.
Which of the following compounds on reaction with methyl magnesium bromide will give tertiary alcohol.
(a) benzaldehyde
(b) propanoic acid
(c) methyl propanoate
(d) acetaldehyde
Answer:
(c) methyl propanoate
Hint:

Hydroxy Compounds And Ethers Question 3.

This ‘X’ is …………..

Answer:

Hint:
hydro boration – Anti markownikoff product
i.e CH₃ – CH₂ – CH – CH₂ – CH₂ – OH

Hydroxy Compounds And Ethers Class 12 Question 4.
In the reaction sequence, Ethane

Ethan – 1, 2 – diol. A and X respectively are ………….
(a) Chioroethane and NaOH
(b) ethanol and H₂SO₄
(c) 2 – chloroethan – 1 – ol and NaHCO₃
(d) ethanol and H₂O
Answer:
(c) 2 – chloroethan – 1 – ol and NaHCO₃
Hint:

12th Chemistry Evaluate Yourself Answers Samacheer Question 5.
Which one of the following is the strongest acid ………..
(a) 2 – nitrophenol
(b) 4 – chlorophenol
(c) 4 – nitrophenol
(d) 3 – nitrophenol
Answer:
(c) 4 – nitrophenol

Hydroxy Compounds And Ethers Important Questions Question 6.

on treatment with Con. H₂SO₄, predominately gives ……………..

Answer:

Hint:

Chemistry Class 12 Ch 11 Notes Question 7.
Carbolic acid is …………..
(a) Phenol
(b) Picric acid
(c) benzoic acid
(d) phenylacetic acid
Answer:
(a) Phenol

Samacheer Kalvi Guru 12th Chemistry Question 8.
Which one of the following will react with phenol to give salicyladehyde after hydrolysis …………..
(a) Dichioro methane
(b) trichioroethane
(c) trichloro methane
(d) CO₂
Answer:
(c) trichloro methane (Riemer Tiemann reaction)
Hint:

11th Chemistry Evaluate Yourself Answers Chapter 11 Question 9.

(a) (CH₃)₃ CCH = CH₂
(b) (CH₃)₂ C = C (CH₃)₂
(c) CH₂ = C(CH₃)CH₂ – CH₂ – CH₃
(d) CH₂ = C (CH₃) – CH₂ – CH₂ – CH₃
Answer:
(b) (CH₃)₂ C = C (CH₃)₂
Hint:

Samacheer Kalvi 12th Chemistry Solutions Question 10.
The correct IUPAC name of the compound,

(a) 4 – chloro – 2, 3 – dimethyl pentan – 1 – ol
(b) 2, 3 – dimethyl – 4 – chloropentan – 1 – ol
(c) 2, 3, 4 – trimethyl – 4 – chiorobutan – 1 – ol
(d) 4 – chioro – 2, 3, 4 – trimethyl pentan – 1 – ol
Answer:
(a) 4 – chloro – 2, 3 – dimethyl pentan – 1 – ol

Hydroxy Compounds Pdf Question 11.
Assertion: Phenol is more acidic than ethanol
Reason: Phenoxide ion is resonance stabilized
(a) if both assertion and reason are true and reason is the correct explanation of assertion.
(b) if both assertion and reason are true but reason is not the correct explanation of assertion.
(c) assertion is true but reason is false
(d) both assertion and reason are false.
Answer:
if both assertion and reason are true and reason is the correct explanation of assertion.

12th Chemistry Evaluate Yourself Answers Question 12.
In the reaction Ethanol
is ………………
(a) ethane
(b) ethoxyethane
(c) ethylbisuiphite
(d) ethanol
Answer:
(d) ethanol
Hint:

Hydroxy Derivatives Class 12 Question 13.
The reaction

can be classified as
(a) dehydration
(b) Williams on alcoholsynthesis
(c) Williamson ether synthesis
(d) dehydrogenation of alcohol
Answer:
(c) Williamson ether synthesis
Hint: Cyclic alcohol → sodium cyclic alkoxide → williamson ether synthesis

Question 14.
Isoprophylbcnzene on air oxidation in the presence of dilute acid gives …………
(a) C₆H₅COOH
(b) C₆H₅COCH₃
(c) C₆H₅COC₆H₅
(d) C₆H₅ – OH
Answer:
(a) C₆H₅ – OH (phenol)

Question 15.
Assertion: Phenol is more reactive than benzene towards electrophilic substitution reaction
Reason: In the case of phenol. the intermediate arenium ion is more stabilized by resonance.
(a) if both assertion and reason are true and reason is the correct explanation of assertion.
(b) if both assertion and reason are true but reason is not the correct explanation of assertion.
(c) assertion is true but reason is false
(d) both assertion and reason are false,.
Answer:
(a) if both assertion and reason are true and reason is the correct explanation of assertion.

Question 16.
HO CH₂ CH₂ – OH on heating with periodic acid gives ………..
(a) methanoic acid
(b) Glyoxal
(c) methanol
(d) CO₂
Answer:
(c) methanol

Question 17.
Which of the following compound can be used as artireeze in automobile radiators?
(a) methanol
(b) ethanol
(c) Neopentyl alcohol
(d) ethan -1, 2-diol
Answer:
(d) ethan -1, 2-diol

Question 18.

is an example of …………..
(a) Wurtz reaction
(b) cyclic reaction
(c) Williamson reaction
(d) Kolbe reactions
Answer:
(c) Kolbe reactions

Question 19.
One mole of an organic compound (A) with the formula C₃H₈O reacts completely with two moles of HI to form X and Y. When Y is boiled with aqueous alkali it forms Z. Z answers the iodoform test. The compound (A) is ……………
(a) propan – 2 – ol
(b) propan- 1- ol
(c) ethoxy ethane
(d) methoxy ehane
Answer:
(d) methoxy ehane
Hint:

Question 20.
Among the following ethers which one will produce methyl alcohol on treatment with hot HI?

Answer:

Hint:

Question 21.
Williamson synthesis of preparing dimethyl ether is a / an /
(a) SN¹ reactions
(b) SN² reaction
(c) electrophilic addition
(d) electrophilic substitution
Answer:
(b) SN² reaction

Question 22.
On reacting with neutral ferric chloride, phenol gives
(a) red colour
(b) violet colour
(c) dark green colour
(d) no colouration
Answer:
(b) violet colour

II. Answer the following questions

Question 1.
IdentIfy the product (s) is / are formed when 1 – methoxy propane is heated with excess HI. Name the mechanism involved in the reaction
Answer:
1-methoxy propane is heated with excess HI, yields two products named as Methyl iodide and 1- iodo propane.
Step 1:

Step 2.

Step 3:

Step 4:

Overall reaction:

This reaction ivvolves nucleophilic substitution reaction mechanism. (SN¹)

Question 2.
Draw the major product formed when 1 – ethoxyprop – 1 – ene is heated with one equivalent of HI
Answer:

This reaction follows SN¹ mechanism because in this reaction the more stable carbocation is formed that is double bonded carbocation. Therefore, the given molecule reacts with HI to form ethanol and 1- iodo prop – 1 – ene.

Question 3.
Suggest a suitable reagent to prepare secondary alcohol with identical group using Grignard reagent.
Answer:
Acetaldehyde reacts with Grignard reagent to give addition product, which on further undergoes acid hydrolysis to yield secondary alcohol, that is isopropyl alcohol.

Question 4.
What is the major product obtained when two moles of ethyl magnesium bromide is treated with methyl benzoate followed by acid hydrolysis
Answer:

Question 5.
Predict the major product, when 2-methyl but – 2 – ene is converted into an alcohol in each of the following methods.

1. Acid catalysed hydration
2. Hydroboration
3. Hydroylation using bayers reagent

Answer:
1. Acid catalysed hydration:

2. Hydroboration.

3. Hydroxylation using bayers reagent:

Question 6.
Arrange the following in the increasing order of their boiling point and give a reason for your ordering

1. Butan – 2 – ol, Butan – 1 – SI, 2 – methylpropan – 2 – ol
2. Propan – 1 – ol, propan – 1, 2, 3 – triol, propan – 1, 3 – diol, propan – 2 – ol

Answer:
1. Boiling points increases regularly as the molecular mass increases due to a corresponding increase in their Van der waal’s force of attraction. Among isomeric alcohols 2° – alcohols have lower boiling points than 1° – alcohols due to a corresponding decreases in the extent

of H-bonding because of steric hindrance. Thus the boiling point of Butan – 2 – ol is lower than that of Butan – 1 – ol. Overall increasing order of boiling points is, 2 – methylpropan – 2 – ol < Butan – 2 – ol < Butan – 1 – ol

2. 2°-alcohols have lower boiling points than 1° – alcohols due to a corresponding decrease in the extent of H – bonding because of steric hindrance. Therefore Propan – 1 – ol has higher boiling point than Propan – 2 – ol. Hydrogen group increases, boiling point also increases. Overall increasing order of boiling points is, propan – 2 – ol < Propan – 1 – ol < propan – 1, 3 – diol < propan -1, 2, 3 – triol

Question 7.
Can we use nucelophiles such as NH₃,CH₃O for the Nucleophilic substitution of alcohols
Answer:
1. Increasing order of nucelophilicity,
NH₃ < – OH^⊕ < CH₃O^⊖-

2. Higher electron density will increase the nucelophilicity.

3. Negatively charged species are almost always more nucelophiles than neutral species.

4. RO^⊖ has an alkyl group attached, allowing a greater amount of polarizability. This means oxygen’s lone pairs will be more readily available to reach in RO^⊖ than in OH^⊖. Hence CH₃O – is the better nucelophile for the nucleophilic substitution of alcohols. NH₃ cannot act as nucelophile for the nucleophilic substitution of alcohols.

Question 8.
Is it possible to oxidise t – butyl alcohol using acidified dichromate to form a carbonyic compound.
Answer:
3° – alcohols do not undergo oxidation reaction under normal condition, but at elevated temperature, under strong oxidising agent cleavage of C – C bond takes place to give a mixture of carboxylic acid.

Yes, it is possible. t – butyl alcohol is readily oxidsing in acidic solution (K₂Cr₂O₇ / H₂SO₄) to a mixture of a ketone and an acid each containing lesser number of carbon atoms than the original alcohol. The oxidation presumably occur via alkenes formed through dehydration of alcohols under acidic conditions.

Question 9.
What happens when 1 – phenyl ethanol is treated with acidified KMnO₄.
Answer:
1 – phenyl ethanol reacts with acidified KMnO₄ to give Acetophenone.

Question 10.
Write the mechanism of acid catalysed dehydration of ethanol to give ethene.
Mechanism of acid catlaysed dehydration of ethanol:
Step1:
Protonation of ethanol.

Step 2:
Elimination of water molecule.

Question 11.
How is phenol prepared form

1. chloro benzene
2. isopropyl benzene

Answer:
1. From Chioro benzene:
According to Dow’s process, when Chiorobenzene is hydrolysed with 6 – 8% NaOHat 300 bar and 633K in a closed vessel, sodium phcnoxidc is formed which on treatment with dilute HCl gives phenol.

2. For isopropyl benzene:
On passing air to a mixture of cumene (isoprophy benzene) and 5% aqueous sodium carbonate solution, cumene hydro peroxide is formed by oxidation. It is treated with dilute acid to get phenol and acetone.

Question 12.
Explain Kolbe’s reaction
Answer:
Kolbe’s (or) Kolbe’s Schmitt reaction:
In this reaction, phenol is first converted into sodium phenoxide which is more reactive than phenol towards electrophilic substitution reaction with CO₂. Treatment of sodium phenoxide with CO₂ at 400K, 4 -7 bar pressure followed by acid hydrolysis gives salicylic acid.
Answer:

Question 13.
Writes the chemical equation for Williamson synthesis of 2 – ethoxy – 2 – methyl pentane starting from ethanol and 2 – methyl pentan – 2 – ol
Answer:
Step 1:

Step 2:

Step 3:

Williamsons synthesis occurs by SN² – mechanism and primary alkyl halides are more reactive in SN² reactions. Therefore ethanol is converted into ethyl bromide.

Question 14.
Write the structure of the aldehyde, carboxylic acid and ester that yield 4 – methylpent – 2 – en – 1 – ol.
Answer:
1. Aldehyde yield 4 – methylpent – 2 – 3n – ol is

2. Acid yield 4 – methylpent – 2 – en – 1 – ol is

3. Ester yield 4 – methylpent – 2 0 en – l – ol is

The above shown compounds undergo reduction reaction to yield 4 – methylpent – 2 – en – l – ol.

Question 15.
What is meta merism? Give the structure and IUPAC name of metamers of 2 – methoxy propane
Answer:
Metamerism:
It is a special type of isomerism in which molecules with same formula, same functional group, but different only in the nature of the alkyl group attached to oxygen.

Ethoxy ethane and 1-methoxy propane are metamers of 2-methoxy propane.

Question 16.
How are the following conversions effected

1. benzylchlorjde to benzvlalcohol
2. benzvl alcohol to benzoic acid

Answer:
1. Conversion of benzyl chloride into benzyl alcohol:

2. Conversion of benzyl alcohol into benzoic acid:

Question 17.
Complete the following reactions

Answer:

Question 18.
O.44g of a monohydric alcohol when added to methyl magnesium iodide in ether liberates at STP 112 cm³ of methane with PCC the same alcohol form a carbonyl compound that answers silver mirror test. Identify the compound.
Answer:
0.44g of a monohydric alcohol liberates 112 cm³ of methane.

Mass of monohydric alcohol which gives 22400 cm3 of methane = \(\frac{22400 \times 0.44}{112}\) = 88
C₅H₁₂O molecular fórmula has mass number 88 and it shows eight possible isomers. But neopentyl alcohol reacts with PCC to form neopentyl aldehyde, which shows positive silver mirror test. Therefore, compound is. neopentyl alcohol (or) 2, 2 – dimethyl propan – l – ol.

Question 19.
Complete the following reactions

Answer:

Question 20.
Phenol is distilled with Zn dust gives (A) followed by friedel – crafts alkylation with propyl chloride to give a compound B, B on oxidation gives (C). Identify A,B and C.
Answer:

Question 21.

Identify A, B, C, D and write the complete equation.
Answer:

Question 22.
What will be the product for the following reaction

Answer:

Question 23.
How will you convert acetylen in to n – butyl alcohol.
Answer:

Question 24.
Predict the product A, B, X and Y in the following sequence of reaction

Answer:

Question 25.
3,3 – dimethylbutan – 2 – ol on treatment with conc. H₂SO₄ to give tetramethyl ethylene as a major product. Suggest a suitable mechanisms
Answer:

According to Saytzeff’s rule the dehydration of 3,3 – dimethylbutan – 2 – ol gives a mixture of alkenes. But the secondary carbocation formed in this reaction undergoes rearrangement to form a more stable tertiary

carbocation which further, undergoes to 13 – elimination leads more stable product, that is 2,3 – dimethyl but – 2 – ene (more yield). According to Saytzeff’s nile, 2, 3 – dimethyl pent- 2 – ene is the major product.

Samacheer Kalvi 12th Chemistry Hydroxy Compounds and Ethers Evaluate yourself

Question 1.
Classify the following alcohols as 1⁰, 2⁰, and 3⁰ and give their IUPAC Names.

Answer:

Question 2.
Write all the possible isomers of an alacohol having the molecular formula C₁₅H₁₂O and their IUPAC names.
Answer:
Eight isomers are possibe for C₁₅H₁₂O. They are,

Question 3.
Suggest a suitable carbonyl compound for the preparation of pent – 2 – en – 1 ol using LiAlH₄.
Answer:

Question 4.
2 – methylpropan – 2 – ene
Answer:

Question 5.
How will you prepare the following using Grignard reagent.

1. t – butyl alcohol
2. allyl alcohol

Answer:

Question 6.
Identify the products in the following reactions. Write their IUPAC names and mention the mechanism involved in the reactions.

Answer:
1.
This reaction involves E₁ – mechanism.

2.
This reaction ivolves SN² – mechanims.

3. Step 1:

Step 2:

This reaction involves SN² Mechanims.

Question 7.
What is the major product obtained when 2,3 – dimethyl pentan – 3 – ol is heated in the presence of H₂SO₄
Answer:

According to Saytzeff’s rule, 2, 3 – dimethyl pent – 2 – ene is the major product.

Question 8.
Which of the following set of reactants will give 1 – methoxy – 4 – nitrobenzene.

Answer:
Step 1:

step 2:

Chemically both sets equally possible. In Set – 1, the Br-atom is activated by electron withdrawing effect of – NO₂ group. Therefore nucleophilic attack by CH₃ONa followed by elimination of NaBr gives the desired ether.

Step 1:

Step 2:

In set – 2, nucleophilic attack by 4 – nitrosodium phenoxide ion on methyl bromide gives the desired ether.

Since alkyl halides (CH₃Br) are more reactive than aryl halides in nucleophilic substitution reactions, therefore set – 2 reactants are preferred.

Question 9.
What happens when m – cresol is treated with acidic solution of sodium dichromate?
Answer:

When m – cresol is treated with acidic solution of sodium dichromate it gives 4 – hydroxy beazoic acid.

Question 10.
When phenol is treated with propan – 2 – ol in the presence of HF, Friedel – Craft reaction takes place. Identify the products.
Answer:

Question 11.
Given the IUPAC name for the following ethers and classify them as simple or mixed.
Answer:

Question 12.
1. Which of the following reaction will give 1 – methoxy – 4 – nitrobenzene.

1. 4 – nitro – 1 – bromobenzene + sodium methoxide.
2. 4 – nitrosodium phenoxide + bromomethane

Answer:
1. Set – 1:

2. set – 2:

Chemically both sets equally possible. In Set – 1, the Br – atom is activated by electron withdrawing effect of – NO₂ group. Therefore nucleophilic attack by CH₃ONa followed by elimination of NaBr gives the desired ether.
Step 1:

Step 2:

In set – 2, nucleophilic attack by 4 – nitrosodium phenoxide ion on methyl bromide gives the desired ether.

Since alkyl halides (CH₃Br) are more reactive than aryl halides in nucleophilic substitution reactions, therefore set – 2 reactants are preferred.

Question 13.
Arrange the following compounds in the increasing order of their acid strength. propan – 1 – ol, 2, 4, 6 – trinitroptienol, 3 – nitrophenol, 3,5 – dinitrophenol, phenol, 4 – methyiphenol.
Answer:
Phenols are stronger acids than alcohols because the phenoxide ion left after the removal of proton is stabilized by resonance while the alkoxide ion left after the removal of a proton from alcohol is not stabilized. Thus propan – 1 – ol is much weaker acid than any phenol.

Thus propan- 1 – ol is a much weaker acid than any phenol. We know that electron donating groups decrease the acidic character and stronger is the electron donating group, weaker is the phenol.

Compare to propan – 1 – ol, 4 – methyl phenol is stronger acidic character. But comparing phenol and 4-methyl phenol, phenol is stronger acidic. Since electron withdrawing groups increase the acidic character of phenols and the effect is more pronounced at the para position than at the meta position.

Therefore 4 – nitro phenol is a stronger acid than 3 – nitro phenol. Further as the number of electron withdrawing groups increases the acidic strength further increases. Therefore 2, 4, 6 – trinitro phenol is a stronger acid than 3, 5 – dintiro phenol. It may be noted here that although the two nitro groups in 3, 5 – dinitro phenol are at m – position with respect to OH group,

their combined effect is however greater than one nitro group at p – position. Therefore 3, 5 – dinitro phenol is a stronger acid than 4-nitro phenol. Thus, the overall increasing order of acid strength is. Propan – 1 – 01 < 4 – methyl phenol < phenol < 3 – nitrophenol < 3, 5 – dinitro phenol < 2, 4, 6 – trinitro phenol.

Question 14.
1 mole of HI is allowed to react with t – butyl methylether. Identify the product and write down the mechanism of the reaction.
Answer:
Step 1:

Step 2

Step 3:

Overall reaction:

Samacheer Kalvi 12th Chemistry Hydroxy Compounds and Ethers Additional Questions

Samacheer Kalvi 12th Chemistry Hydroxy Compounds and Ethers 1 Mark Questions and Answers

I. Choose the best answer.

Question 1.
Which one of the following is a trihydric alcohol?
(a) Glycol
(b) Ethanol
(c) Glycerol
(d) Sorbitol
Answer:
(c) Glycerol

Question 2.
Identify the monohydric unsaturated alcohol.

Answer:

Question 3.
Which one of the following is named as sorbital?

Answer:

Question 4.
Which one of the following is a primary alcohol?

Answer:

Question 5.
Which of the following is a dihydric alcohol?
(a) Ethenol
(b) Ethanol ]
(c) Ethane – 1, 2 – diol
(d) Propan – 2 – ol
Answer:
(c) Ethane – 1, 2 – diol

Question 6.
Which one of the following is an example of secondary (2°) alcohol?
(a) Propan – 2 – ol
(b) Phenyl methanol
(c) Ethenol
(d) 2 – methyl – propan – 2 – ol
Answer:
(a) Propan – 2 – ol

Question 7.
Which one of the following is a tertiary alcohol?

Answer:

Question 8.
Which of the following is a primary alcohol?

Answer:

Question 9.
Which one of the following find application in proper functioning of our eyes?
(a) Cholesterol
(b) Retinol
(c) Phenol
(d) Ethanol
Answer:
(b) Retinol

Question 10.
Which is the storage of vitamin – A?
(a) Retinol
(b) Benzyl alcohol
(c) Phenol
(d) Ascorbic acid
Answer:
(a) Retinol

Question 11.
The important component in our cell membrane is ………….
(a) Retinol
(b) Phenol
(c) Cholesterol
(d) Methanol
Answer:
(c) Cholesterol

Question 12.
Which acts as an additive to petrol?
(a) Glycerol
(b) Ethanol
(c) Phenol
(d) Methanol
Answer:
(b) Ethanol

Question 13.
Which one of the following vitamin is stored in Retinol?
(a) Vitamin – B₁₂
(b) Vitamin – A
(c) Vitamin – C
(a) Vitamin – D
Answer:
(b) Vitamin – A

Question 14.
Which alcohol is used as skin cleanser for injection?
(a) Methanol
(b) Ethanol
(c) 1 -propanol
(d) 2-propanol
Answer:
(d) 2-propanol

Question 15.
Which one of the following is used as an industrial solvent?
(a) Methanol
(b) Benzyl alcohol
(c) Phenol
(d) Cholesterol
Answer:
(a) Methanol

Question 16.
2 – methyl but – 3 – en – 2 – ol belongs to which type of alcohol?
(a) 3° alcohol
(b) 2° alcohol
(c) 1° alcohol
(d) Aromatic alcohol
Answer:
(a) 3° alcohol

Question 17.
The IUPAC name of

(a) 1 – methyl – 2 – propanol
(b) 2 – methyl – p ropan – 2 – ol
(c) Tertibutyl alcohol
(d) 2 – propanol
Answer:
(b) 2 – methyl – p ropan – 2 – ol

Question 18.
The TUPAC name of CH₂ = CH – CH₂OH is …………
(a) Allyl alcohol
(b) Propenc – 2 – ol
(c) Prop – 2 – en – 1 – oI
(d) Isopropyl alcohol
Answer:
(c) Prop – 2 – en – 1 – oI

Question 19.
In methanol, – OH group attached to carbon is ………..
(a) sp hybridised atom
(b) sp³ hybridised atom
(c) sp² hybridised atom
(d) dsp² hybridised atom
Answer:
(c) sp² hybridised atom

Question 20.
Which one of the following is C – O – H bond angle in methanol?
(a) 109.5°
(b) 104°
(c) 90°
(d) 108.9°
Answer:
(d) 108.9°

Question 21.
Primaiy alkyl halides undergoes substitution by ……….
(a) SN¹ reaction
(b) SN_i reaction
(c) SN² reaction
(d) SN reaction
Answer:
(c) SN² reaction

Question 22.
What is the product formed when propene is hydrolysed in the presence of mineral acid?
(a) Propan – 1 – ol
(b) Propan – 2 – ol
(c) Iso butyl alcohol
(d) 2 – mcthyl – propan – 2 – ol
Answer:
(b) Propan – 2 – ol

Question 23.
The product formed when phenyl magnesium bromide treated with methanal and hydrolysed is ………..
(a) Phenyl methanal
(b) Phenol
(c) Phenyl methanol
(d) Benzyl benzoate
Answer:
(c) Phenyl methanol

Question 24.
To get Butan – 2 – ol, Ethyl magnesium bromide is treated with followed by hydrolysis.
(a) HCHO
(b) CH₃COCH₃
(c) CO₂
(d) CH₃CHO
Answer:
(d) CH₃CHO

Question 25.
Which one of the following is formed when Butyl magnesium bromide is treated with propanone followed by hydrolysis?
(a) Tertiary butyl alcohol
(b) Isopropyl alcohol
(c) 2 – methyl hexan – 2 – ol
(d) Propan – 1 -ol
Answer:
(c) 2 – methyl hexan – 2 – ol

Question 26.
Which one of the tbllowing is used to get propan – 2 – ol by the reaction with CH₃MgBr?
(a) Ethanol
(b) Ethanal
(c) Ethyl inethanoate
(d) Propanone
Answer:
(c) Ethyl inethanoate

Question 27.
Crotanaldehyde on reaction with LiAlH₄ and water produces
(a) Ethanol
(b) Propan – 2 – ol
(c) Methanol
(d) But – 2 – en – 1 – ol
Answer:
(d) But – 2 – en – 1 – ol

Question 28.
Which one of the following is used as a catalyst in the conversion of Bcnzoic acid to Benzyl alcohol?
(a) Ni
(b) LiAIH₄ / H₂O
(c) Sn / HCI
(d) Zn / NaOH
Answer:
(b) LiAIH₄ / H₂O

Question 29.
What is the product formed when acetone is treated with LiA1H4 and 1120?
(a) Isobutyl alcohol
(b) n – butyl alcohol
(c) Propan – 2 – ol
(d) Propan – 1 – ol
Answer:
(c) Propan – 2 – ol

Question 30.
Which one of the following is formed when ethene reacts with Baeyer’s reagent?
(a) Ethane
(b) Ethylene glycol
(c) Propane – 1, 2 – diol
(d) Glycerol
Answer:
(b) Ethylene glycol

Question 31.
Which one of the following is named as Baeyer’s reagent?
(a) acidified K₂Cr₂O₇
(b) acidified KMnO₄
(c) Cold dilute alkaline KMnO₄
(d) LiAlH₄
Answer:
(c) Cold dilute alkaline KMnO₄

Question 32.
The alkaline hydrolysis of fats to give glycerol is known as …………
(a) Esterification
(b) Hydroboration
(c) Hydration
(d) Saponification
Answer:
(d) Saponification

Question 33.
Which one of the following alcohol reacts immediately with Lucas reagent?
(a) Primaiy alcohol
(b) Tertiary alcohol
(c) Phenol
(d) Secondary alcohol
Answer:
(b) Tertiary alcohol

Question 34.
Which one of the following is called Lucas reagent?
(a) Conc. HCl + Anhydrous ZnCl₂
(b) Conc. HCl + Anhydrous A1CI₃
(c) LiAIH₄ + H₂O
(d) Cold dilute alkaline KMnO₄
Answer:
(a) Conc. HCl + Anhydrous ZnCl₂

Question 35.
Which alcohol gives red colour in Victor Meyer’s test?
(a) 2° alcohol
(b) 3° alcohol
(c) Phenol
(d) 1° alcohol
Answer:
(d) 1° alcohol

Question 36.
Which colour is given by secondary alcohol in Victor Meyer’s test?
(a) Red
(b) Green
(c) Blue
(d) Yellow
Answer:
(c) Blue

Question 37.
Which mechanism is followed in the reaction of 2 – methyl – 2 – propanol with HBr?
(a) E₁ mechanism
(b) E₂ mechanism
(c) SN² mechanism
(d) SN¹ mechanism
Answer:
(d) SN¹ mechanism

Question 38.
Which mechanism is followed in the conversion of ethanol to bromoethane by HBr?
(a) SN¹ mechanism
(b) SN² mechanism
(c) E₁ mechanism
(d) E₂ mechanism
Answer:
(c) E₁ mechanism

Question 39.
Which one of the following is used as a catalyst in the reaction of methanol with thionyl chloride?
(a) Pyridine
(b) pyrrole
(c) THF
(d) Nickel
Answer:
(a) Pyridine

Question 40.
The mechanism of the reaction of ethanol with PCl₃ is ……………..
(a) SN¹
(b) SN²
(c) E₂
(d) E₁
Answer:
(b) SN²

Question 41.
Which one of the following reagent is used in the conversion of Ethanol to ethene?
(a) Zn + Hg / H₂O
(b) LiAlH₄
(c) acidified K₂Cr₂O₇
(d) Conc. H₂SO₄
Answer:
(d) Conc. H₂SO₄

Question 42.
Primary alcohol undergo dehydration by ………
(a) E₁ mechanism
(b) E₂ mechanism
(c) SN¹ mechanism
(d) SN² mechanism
Answer:
(b) E₂ mechanism

Question 43.
Tertiary alcohols undergo dehydration by ……….
(a) SN¹ mechanism
(b) E₂ mechanism
(c) E₁ mechanism
(d) SN² mechanism
Answer:
(c) E₁ mechanism

Question 44.
Which one of the following is the correct order of relative reactivities of alcohols in the dehydration reaction?
(a) 1° < 2° < 3°
(b) 2° < 1° < 3°
(c) 3° < 2° < 1°
(d) 3° < 1° < 2°
Answer:
(a) 1° < 2° < 3°

Question 45.
Which of the following is the product formed when 3,3 – dimethyl – 2 – butanol reacts with conc.H₂SO₄?
(a) 2, 3 – dirnethyl but – 1 – ene
(b) 2,3 – dimethyl but – 2 – ene
(c) 3, 3 – dimethyl but – 1 – ene
(d) all the above
Answer:
(d) all the above

Question 46.
The oxidising agent used to prepare aldehyde (or) ketone from alcohol, the reagent used is …………..
(a) acidified Na₂Cr₂O₇
(b) alkaline KMnO₄
(c) Pyridinium chlorochromate
(d) conc. H₂SO₄
Answer:
(c) Pyridinium chlorochromate

Question 47.
The product formed when propan – 2 – ol is treated with dimethyl sulfoxide (DMSO) and oxalyl chloride followed by the addition of Et₃N is ……….
(a) Oxalyl chloride
(b) Propanal
(c) Ethanoic aicd
(d) Propanone
Answer:
(d) Propanone

Question 48.
Which reaction is used to convert alcohol to ketone / aldehyde in the presence of DMSO?
(a) Lucas test
(b) Swern oxidation
(c) Biological oxidation
(d) Kolbe’s reaction
Answer:
(b) Swern oxidation

Question 49.
Which product is formed when propan- 1 – ol is oxidised by pyridinium chlorochromate (PCC)?
(a) Propanal
(b) Propanone
(c) Propane
(d) Propene
Answer:
(a) Propanal

Question 50.
Which one of the enzyme is produced in liver to detoxify the alcohol?
(a) Diastase
(b) Zymase
(c) Invertase
(d) Dehydrogenase alcohol
Answer:
(d) Dehydrogenase alcohol

Question 51.
What isADH and NAD?
(a) Alcohol dehydrogenase and nicotinamide adenine dinucleotide
(b) Acid dehydration and Nitrogen addition
(c) Alcohol dehydration and Nicotine addition
(d) Adeninc hydrogenase and Nicotinamide adenine dinucleotide
Answer:
(a) Alcohol dehydrogenase and nicotinamide adenine dinucleotide

Question 52.
What is the main reaction take place when 2 – methyl propan – 2 – ol reacts with Cu at 573 K?
(a) Dehydrogenation
(b) Oxidation
(c) Dehydration
(d) Hydrogenation
Answer:
(c) Dehydration

Question 53.
Name the product formed when tertiary butyl alcohol is treated with Cu at 573 K?
(a) 2 – methyl prop – 1 – ene
(b) 2 – methyl prop – 2 – ene
(c) propene
(d) 1 – butene
Answer:
(a) 2 – methyl prop – 1 – ene

Question 54.
Which one of the following product is formed when propan – 2 – ol is treated with Cu at 573 K?
(a) Propanal
(b) Propanone
(c) Propan – 1 – ol
(d) Propane
Answer:
(b) Propanone

Question 55.
What is the name of the reaction between ethanol and ethanoic acid?
(a) Esterification
(b) Saponification
(c) Ethenfication
(d) Hydroxylation
Answer:
(a) Esterification

Question 56.
Which one of the following is formed when ethan – 1, 2 – diol is treated with PI₃?
(a) Ethane
(b) Ethyne
(c) Ethene
(d) Ethanol
Answer:
(c) Ethene

Question 57.
Which reagent is used to convert ethylene glycol to ethylene?
(a) HI
(b) I₂
(c) PI₃
(d) Conc. H₂ SO₄
Answer:
(c) PI₃

Question 58.
What is the product formed when ethylene glycol is heated at 773 K?
(a) Ethanal
(b) Ethene
(c) Ethane
(d) Oxirane
Answer:
(d) Oxirane

Question 59.
Which reagent is used to convert ethan – 1, 2 – diol into Ethanal?
(a) Anhydrous ZnCI₂
(b) Dilute. H₂SO₄
(c) Either (a) or (b)
(d) Conc. H₂SO₄
Answer:
(c) Either (a) or (b)

Question 60.
Name the product formed when ethan- 1, 2-diol is treated with anhydrous ZnCl₂.
(a) Ethanol
(b) Ethene
(c) Ethane
(d) Ethanal
Answer:
(d) Ethanal

Question 61.
Which one of the following is formed when ethane – 1, 2 – diol is treated with Conc. H₂ SO₄?
(a) 1, 4 – dioxane
(b) Ethanal
(c) Ethanoic acid
(d) Ethene
Answer:
(a) 1, 4 – dioxane

Question 62.
Which one of the following is formed when ethylene glycol is treated with periodic acid?
(a) Methanal
(b) Methanol
(c) Ethanol
(d) Ethanal
Answer:
(a) Methanal

Question 63.
Identify the product formed when glycerol is treated with nitric acid and conc. H₂SO₄?
(a) Nitroglycerine
(b) Glyceryl triacetate
(c) Prop – 2 – enal
(d) Glyceric acid
Answer:
(a) Nitroglycerine

Question 64.
What will be the product formed when propan – 1, 2, 3 – triol is treated with KHSO₄?
(a) Nitroglycerine
(b) TNG
(c) Prop – 2 – enal
(d) Allyl alcohol
Answer:
(a) Nitroglycerine

Question 65.
Oxidation of glycerol with dil.HNO₃ gives ………
(a) Meso oxalic acid
(b) Glyceric acid and tartronic acid
(c) Glycerose
(d) Glyceraldehyde and dihydroxy acetone
Answer:
(b) Glyceric acid and tartronic acid

Question 66.
Oxidation of glycerol with Fenton reagent gives ………..
(a) Glyceraldehyde + Dihydroxy acetone
(b) Glyceric acid + Tartronic acid
(c) Meso oxalic acid
(d) Oxalic acid
Answer:
(a) Glyceraldehyde + Dihydroxy acetone

Question 67.
Which one of the following product is formed when glycerol is oxidised with acidified KMnO₄?
(a) Meso oxalic acid
(b) Oxalic acid
(c) Formic acid
(d) Glyceric acid
Answer:
(b) Oxalic acid

Question 68.
Which one of the following is used as a solvent for paints, varnishes and gum?
(a) Ethanol
(b) Methanol
(c) Methanal
(d) Ethanal
Answer:
(b) Methanol

Question 69.
Which one of the following is used as fuel for aeroplane?
(a) Methanol + Ethanol
(b) Ethanol + Petrol
(c) Ethanol + Propanol
(d) Butanol + Methanol
Answer:
(b) Ethanol + Petrol

Question 70.
Which one of the following is used as beverage as well as preservative for biological specimens?
(a) Ethanol
(b) Methanol
(c) Phenol
(d) Benzyl alcohol
Answer:
(a) Ethanol

Question 71.
Which one of the following is used as an anti-freezer in automobile radiator?
(a) Glycerol
(b) Phenol
(c) Benzyl alcohol
(d) Ethylene glycol
Answer:
(d) Ethylene glycol

Question 72.
Which one of the following is used as a sweetening agent in confectionery and beverages?
(a) Glycerol
(b) Phenol
(c) Benzyl alcohol
(d) Ethylene glycol
Answer:
(a) Glycerol

Question 73.
Which one of the following is used in the manufacture of cosmetics and transparent soaps?
(a) Methanol
(b) Ethanol
(c) Glycerol
(d) Phenol
Answer:
(c) Glycerol

Question 74.
Which one of the following is used in the manufacture of explosive dynamite and cordite by mixing it with clay?
(a) Glycol
(b) Glycerol
(c) Ethanol
(d) Benzaldehyde
Answer:
(b) Glycerol

Question 75.
Which alcohols is used in making printing inks and stamp pad ink?
(a) Glycol
(b) Ethanol
(c) Glycerol
(d) Phenol
Answer:
(c) Glycerol

Question 76.
Except which alcohol, other alcohols are weaker acid than water?
(a) Ethanol
(b) Phenol
(c) Methanol
(d) Propanol
Answer:
(c) Methanol

Question 77.
Which one of the following is the correct decreasing order of acidity in alcohol?
(a) 1° alcohol > 2° alcohol > 3° alcohol
(b) 3° alcohol > 2° alcohol> 1° alcohol
(c) 2° alcohol> 1° alcohol > 3° alcohol
(d) 3° alcohol > 1° alcohol > 2° alcohol
Answer:
(a) 1° alcohol > 2° alcohol > 3° alcohol

Question 78.
Which one of the following is more acidic?
(a) Benzyl alcohol
(b) Phenol
(c) Ethanol
(d) Methanol
Answer:
(b) Phenol

Question 79.
The JUPAC name of Phioroglucinol is ………….
(a) 4 – methyl phenol
(b) 1, 4 – dihydroxy benzene
(c) 1, 3, 5 – trihydroxy benzene
(d) 1, 2, 3 – trihydroxy benzene
Answer:
(c) 1, 3, 5 – trihydroxy benzene

Question 80.
The other name of 1 , 2, 3 – trihydroxy benzene is called ……….
(a) Pholoroglucinol
(b) Quinol
(c) Pyrogallol
(d) Hydroxy quinol
Answer:
(c) Pyrogallol

Question 81.
The other name of 3, 5 – dihydroxy toluene is known as …………
(a) Orcinol
(b) Quinol
(c) Pyrogallol
(d) Resorcinol
Answer:
(a) Orcinol

Question 82.
The IUPAC name of Catechol is known as ………..
(a) 1 , 3 – dihydroxy benzene
(b) 1, 2 – dihydroxy benzene
(c) 1, 4 – dihydroxy benzene
(d) 1, 3, 5 – trihydroxy benzene
Answer:
(b) 1, 2 – dihydroxy benzene

Question 83.
The name of

is …………
(a) Phloroglucinol
(b) pyrogallol
(c) Quinol
(d) Resorcinol
Answer:
(a) Phloroglucinol

Question 84.
The name of

(a) Pyrogallol
(b) Hydroxy cresol
(c) Orcinol
(d) Phloroglucinol
Answer:
(c) Orcinol

Question 85.
The reaction of chiorobenzene with NaOH is known as ………..
(a) Kolbe’s reaction
(b) Riemcr – Ticmann reaction
(c) Dow’s process
(d) Cumene synthesis
Answer:
(c) Dow’s process

Question 86.
Which one of the product is formed when benzene and propene is heated at 523 K?
(a) Cumene
(b) 2 – ethyl benzene
(c) 2 – propyl benzene
(d) Ethyl enthanoate
Answer:
(a) Cumene

Question 87.
What will be the product formed when phenol is treated with zinc dust?
(a) Cumene
(b) Toluene
(c) Ethyl benzene
(d) Benzene
Answer:
(d) Benzene

Question 88.
The acetylation and benzoylation of phenol are called ……….
(a) Dow’s process
(b) Schotten – Baumann reaction
(c) Reimer – Tiemann reaction
(d) Williamson ether synthesis
Answer:
(b) Schotten – Baumann reaction

Question 89.
Name the product formed when phenol is heated with ammonia in the presence of anhydrous
ZnCl₂.
(a) Benzene
(b) Aniline
(c) Anisole
(d) Phenyl acetate
Answer:
(b) Aniline

Question 90.
What will be the product formed when phenol is treated with benzoyl chloride in the presence of a base?
(a) Phenyl acetate
(b) Phenyl cnthanoatc
(c) Phenyl benzoate
(d) Benzyl acetate
Answer:
(c) Phenyl benzoate

Question 91.
Which one of the following is formed when phenol istreated with acidified K₂Cr₂O₇?
(a) Benzoic acid
(b) Phenyl amine
(c) Phenyl acetate
(d) 1, 4 – benzo quinone
Answer:
(d) 1, 4 – benzo quinone

Question 92.
Hydrogenation of phenol in the presence of Nickel gives ………
(a) cyclo hexane
(b) cyclo hexanol
(c) benzene
(d) cumene
Answer:
(b) cyclo hexanol

Question 93.
Which one of the following is formed when phenol reacts with a mixture of Conc. HNO₃ and Conc.H₂SO₄?
(a) Ortho nitro phenol
(b) Para nitro phenol
(c) 1, 2 – dinitro phenol
(d) 2, 4 , 6 – trinitro phenol
Answer:
(d) 2, 4 , 6 – trinitro phenol

Question 94.
What will be the product formed when phenol reacts with bromine water?
(a) 0 – bromo phenol
(b) P – bromo phenol
(c) 1, 3, 5 – tri bromo phenol
(d) 2, 4, 6 – tri bromo phenol
Answer:
(d) 2, 4, 6 – tri bromo phenol

Question 95.
The conversion reaction of phenol of salicylic acid is known as
(a) Schottan – Baumann reaction
(b) Riemer – Ticmann reaction
(c) Kolbe’s Schmitt reaction
(d) Williamson’s synthesis
Answer:
(c) Kolbe’s Schmitt reaction

Question 96.
The reagent used for the conversion of phenol into salicylaldehyde is ………..
(a) CHCI₃ / NaOH
(b) I₂ / KOH
(c) Zn
(d) Br₂ / CCl₄
Answer:
(a) CHCI₃ / NaOH

Question 97.
What is the name of the reaction of phenol with chloroform and aqueous alkali?
(a) Kolbe’s reaction
(b) Cumene synthesis
(c) Rlemer – Tiemann reaction
(d) Schottan – Baumann reaction
Answer:
(c) Rlemer – Tiemann reaction

Question 98.
Which one of the following is formed when phenol is treated with chloroform and sodium hydroxide.
(a) Chiorobenzene
(b) Salicylaldehyde
(c) Salicylic acid
(d) Aniline
Answer:
(b) Salicylaldehyde

Question 99.
What are the reagents required to prepare phenolphthalein?
(a) Phenol + Phthalic acid
(b) Phenol + Benzene
(c) Phenol + Phthalic anhydride
(d) Phenol + Aniline
Answer:
(c) Phenol + Phthalic anhydride

Question 100.
Which one of the following is formed when Phenol reacts with benzene diazonium chloride?
(a) P – hyclroxy diazo phenol
(b) P – hydroxy azo benzene
(c) O – hydroxy benzene
(d) O – hydroxy azo benzene
Answer:
(b) P – hydroxy azo benzene

Question 101.
Which reagent gives purple colouration with phenol?
(a) Anhydrous AlCl₃
(b) Anhydrous ZnCl₂
(c) Neutral FeCI₃
(d) HCI + ZnCI₂
Answer:
(c) Neutral FeCI₃

Question 102.
Bakelite is formed when phenol reacts with ………..
(a) Methanol
(b) Methanal
(c) Ethanal
(d) Ethanol
Answer:
(b) Methanal

Question 103.
Which one of the following is used as an antiseptic – carbolic lotion and carbolic soaps?
(a) Benzyl alcohol
(b) Methanol
(c) Glycol
(d) Phenol
Answer:
(d) Phenol

Question 104.
The product formed when formaldehyde reacts with phenol is ……..
(a) Bakelite
(b) Phenolphthalein
(c) Azodye
(d) Aniline
Answer:
(a) Bakelite

Question 105.
Which one of the following is a simple ether?

Answer:

Question 106.
Which one of the following is an example for mixed ether?
(a) Methoxy methane
(b) Phenoxy benzene
(c) Methoxy benzene
(d) Ethoxy ethane
Answer:
(c) Methoxy benzene

Question 107.
The IUPAC name of

(a) 1 – methoxyl isopropyl ethane
(b) 2 – methoxy – 2 – methyl propane
(c) 2, 2 – dimethyl 2- methoxy ethane
(d) Methoxy tertiary butane
Answer:
(b) 2 – methoxy – 2 – methyl propane

Question 108.
The IUPAC name of C₆H₅ – O – C₆H₅ is ……..
(a) Diphenyl ether
(b) Phenoxy methane
(c) Phenoxy benzene
(d) Ethoxy benzene
Answer:
(c) Phenoxy benzene

Question 109.
Which one of the following is not a simple ether?
(a) C₆H₅ – O – CH₂ – CH₃
(b) CH₃ – O – CH₃
(c) C₆H₅ – O – C₆H₅
(d) C₂H₅ – O – C₂H₅
Answer:
(a) C₆H₅ – O – CH₂ – CH₃

Question 110.
What is the name of the reaction when ethanol is treated with Conc.H₂SO₄ at 413 K?
(a) Intermolecular dehydration
(b) Intra – molecular dehydration
(c) Dehydrogenation
(d) Dehydro halogenation
Answer:
(a) Intermolecular dehydration

Question 111.
Identify the product formed when ethanol is treated with Conc.H₂SO₄ at 413 K?
(a) Ethene
(b) Ethane
(c) 2 – butanol
(d) Diethyl ether
Answer:
(d) Diethyl ether

Question 112.
The reaction of sodium methoxide with ethyl bromide follows
(a) SN¹ mechanism
(b) SN² mechanism
(c) E₁ reaction
(d) E₂ reaction
Answer:
(b) SN² mechanism

Question 113.
The product formed when tertiary butyl bromide and sodium methode are react together is ……….
(a) 2 – methyl – 2 – methoxy propane
(b) ethoxy ethane
(c) 2 – methyl – prop – 1 – ene
(d) 2 – methyl but – 1 – ene
Answer:
(c) 2 – methyl – prop – 1 – ene

Question 114.
Identify the product formed when diazomethane reacts with Ethanol in the presence of HBF₄?
(a) Methoxy ethane
(b) Ethoxy ethane
(c) Diethyl ether
(d) Ethyl isopropyl ether
Answer:
(a) Methoxy ethane

Question 115.
What arc the products formed when methoxy ethanc is treated with hydroiodic acid?
(a) Phenol + iodomethane
(b) Todomethane + Ethanol
(c) lodoethane + Methanol
(d) lodobenzene + Methane
Answer:
(b) Todomethane + Ethanol

Question 116.
What are the products formed when methoxy benzene is treated with HI?
(a) C₆H₅OH + CH₄
(b) CH₃I + C₆H₆
(c) C₆H₅ OH + CH₃I
(d) C₂H₅I + C₆H₆
Answer:
(c) C₆H₅ OH + CH₃I

Question 117.
The mechanism involved in Williamson’s synthesis is …………
(a) E₁
(b) E₂
(c) SN²
(d) SN¹
Answer:
(c) SN²

Question 118.
When diethyl ether is exposed to excess oxygen, the reaction taken place is …………
(a) reduction
(b) hydrogenation
(c) dehydrogenation
(d) auto oxidation
Answer:
(d) auto oxidation

Question 119.
Which one of the following is formed when Diethyl ether is treated with dil.H₂SO₄?
(a) CH₃CH₂HSO₄
(b) CH₃ – CH₂OH
(c) CH₂ = CH₂
(d) CH₃ – CH₃
Answer:
(b) CH₃ – CH₂OH

Question 120.
Which one of the following is formed when diethyl ether reacts with Cl2 in the presence of light?

Answer:

Question 121.

In the above reaction A and B are
(a) CH₃ CH₂ OH + CH₃ – CH₂ Cl
(b) CH₃ – CH₂Cl + CH₃ COOH
(c) CH₃ COOH + CH₃ COOCH₃
(d) CH₃ – CH₂CI + CH₃COOCH₂CH₃
Answer:
(d) CH₃ – CH₂CI + CH₃COOCH₂CH₃

Question 122.
Anisole undergoes bromination with Br₂ in acetic acid in the absence of catalyst, the major product formed is ………..
(a) O – bromoan isole
(b) P – bromoan isole
(c) Benzyl bromide
(d) Bromo benzene
Answer:
(b) P – bromoan isole

Question 123.
Anisole reacts with methyl chloride in the presence of anhydrous AICI₃ and CS₂ to give ……..
(a) 2 – methoxy toluene
(b) 4 – methoxy toluene
(c) either (a) or (b)
(d) both (a) and (b)
Answer:
(d) both (a) and (b)

Question 124.
Which one of the following is used as a surgical anesthetic agent in surgery?
(a) Ethanol
(b) Ethoxy ethane
(c) Methoxy ethane
(d) Methoxy propane
Answer:
(b) Ethoxy ethane

Question 125.
Which one of the following is a precursor to the synthesis of perfumes and insecticide pheromones?
(a) Phenol
(b) Benzyl alcohol
(c) Anisole
(d) Diethyl ether
Answer:
(c) Anisole

Question 126.
Among the alkenes which one produces tertiary butyl alcohol on acid hydration?
(a) (CH₃)₂C CH₂
(b) CH₃ – CH = CH – CH₃
(c) CH₃ – CH₂ – CH = CH₂
(d) CH₃ – CH = CH₂
Answer:
(a) (CH₃)₂C CH₂

Question 127.
An ether is more volatile than an alcohol having the same molecular formula. This is due to
(a) dipolar character of ethers
(b) alcohols having resonance structures
(c) inter molecular hydrogen bonding in ethers
(d) inter molecular hydrogen bonding in alcohols
Answer:
(d) inter molecular hydrogen bonding in alcohols

Question 128.
An organic compound A containing C, H and O has a pleasant odour. On boiling A with Conc.H₂SO₄, a colourless gas is produced which decolourises bromine water and alkaline KMnO₄. The organic liquid A is ………..
(a) C₂H₅COOCH₃
(b) C₂HOH
(c) C₂H₅CI
(d) C₂H₆
Answer:
(b) C₂HOH

Question 129.
Chloroethane reacts with X to form diethyl ether. What is X?
(a) NaOH
(b) H₂SO₄
(c) C₂H₅ONa
(d) C₂H₅Cl
Answer:
(c) C₂H₅ONa

Question 130.
In the following sequence of reactions,

the compound D is ……….
(a) Butanal
(b) n-butyl alcohol
(c) propan – 1 – ol
(d) Propanal
Answer:
(c) propan – 1 – ol

Question 131.
Propan – 1 – ol and Propan – 2 – ol can be chemically distinguished by which reagent?
(a) PCI₅
(b) Reduction
(c) Oxidation with K₂ Cr₂0₇
(d) Ozonolysis
Answer:
(c) Oxidation with K₂ Cr₂0₇

Question 132.
Phenol can be distinguished from ethanol by the following reagents except
(a) Sodium
(b) NaOH / I₂
(c) Neutral FeCI₃
(d) Br₂ / H₂O
Answer:
(a) Sodium

Question 133.
in cold countries, ethylene glycol is added to water in the radiators to …………
(a) bring down the specific heat of water
(b) lower the viscosity
(c) reduce the viscosity
(d) make water a better lubricant
Answer:
(a) bring down the specific heat of water
(i.e.) lowering down the freezing point of water.

Question 134.
Main constituent of dynamite is ………..
(a) nitro benzene
(b) nitro glycerine
(c) Picric acid
(d) TNT
Answer:
(b) nitro glycerine

Question 135.
Diethyl ether finds use in medicine as …………
(a) a pain killer
(b) a hypnotic
(c) an antiseptic
(d) an anaesthetic
Answer:
(d) an anaesthetic

Question 136.
Benzene diazonium chloride on reaction with phenol in weakly basic medium gives
(a) Diphenyl ether
(b) P – hydroxy azo benzene
(c) Chlorobenzene
(d) Benzene
Answer:
(b) P – hydroxy azo benzene

Question 137.
The alcohol that produces turbidity immediately with ZnCl₂ + Conc.HCl at room temperature is ………..
(a) Rutan – 1- ol
(b) Butan – 2- ol
(c) 2 – methyl – propan – 1 – ol
(d) 2 – methyl – propan – 2 – ol
Answer:
(d) 2 – methyl – propan – 2 – ol

Question 138.
Propanone is the product obtained by dehydrogenation of …………
(a) Propan – 2 – ol
(b) Propan – 1 – ol
(c) Propanal
(d) n – propyl alcohol
Answer:
(a) Propan – 2 – ol

Question 139.
Which of the following statement is correct?
(a) Phenol is less acidic than ethanol
(b) Phenol is more acidic than ethanol
(c) Phenol is more acidic than carboxylic acid
(d) Phenol is less acidic than carboxylic acid
Answer:
(b) Phenol is more acidic than ethanol

Question 140.
The reaction of ethylene glycol with Pl₃ gives ………..
(a) CH₂ = CHI
(b) ICH₂ – CH₂I
(c) CH₂ = CH2₂
(d) CH = CH
Answer:
(a) CH₂ = CHI

Question 141.
During dehydration of alcohols to alkenes by heating with Conc. H₂SO₄ ,the initiation step is ………..
(a) protonatlon of alcohol
(b) formation of carbocation
(c) elimination of water
(d) formation of carbanion
Answer:
(a) protonatlon of alcohol

Question 142.
Sodium phenoxide reacts with CO₂ at 400 K and 4 – 7 bar pressure to give ………
(a) Sodium salicylate
(b) Salicylaldehyde
(c) Cate chol
(d) Pyrogallol
Answer:
(a) Sodium salicylate

Question 143.
The reaction of C₂ H₅OH with Cone. H₂ SO₄ does not give ………..
(a) Ethylene
(b) Diethyl ether
(c) Acetylene
(d) Ethyl hydrogen sulphate
Answer:
(c) Acetylene

Question 144.
Which of the following gives ketone on oxidation?

Answer:

Question 145.
Phenol is treated with Br₂ /H₂O and shaken well. The white precipitate formed during the process is …………
(a) m – bromo phenol
(b) 2,4 – dibromo phenol
(c) 2, 4, 6 – tribromo phenol
(d) 1, 2 – dibromo benzene
Answer:
(c) 2, 4, 6 – tribromo phenol

Question 146.
Which compound has the highest boiling point?
(a) Acetone
(b) Diethyl ether
(c) Methanol
(d) Ethanol
Answer:
(d) Ethanol

Question 147.
When phenol reacts with NH₃ in the presence of ZnCl₂ at 300°C, it gives ………..
(a) 1° amine
(b) 2° amine
(c) 3° amine
(d) Both (b) and (c)
Answer:
(a) 1° amine

Question 148.
Azo dyes are prepared from …………
(a) Aniline + Phenol
(b) Phenol + Phthalic anhydride
(c) Phenol + Benzene diazonium chloride
(d) Aniline + Phthalic anhydride
Answer:
(c) Phenol + Benzene diazonium chloride

Question 149.
A compound that easily undergoes bromination is ………….
(a) Phenol
(b) Toluene
(c) Benzene
(d) Diethyl ether
Answer:
(a) Phenol

Question 150.
When glycerol is treated with P₂O₅ (or) KHSO₄ the product formed is ……….
(a) CH₂ = CH – CH₃
(b) CH₂ = CH – CH₂OH
(c) CH₂ = CH – CHO
(d) CH₂ = C = CH₂
Answer:
(c) CH₂ = CH – CHO

Question 151.
The ether that undergoes electrophilic substitution reactions is ………….
(a) CH₃ – O – C₂H₅
(b) C₆H₅ – O – CH₃
(c) C₂H₅ – O – C₂H₅
(d) CH₃ – O – CH₃
Answer:
(b) C₆H₅ – O – CH₃

Question 152.
With anhydrous ZnCl₂, ethylene glycol gives …………
(a) Formaldehyde
(b) Acetylene
(c) Acetaldehyde
(d) Dioxan
Answer:
(c) Acetaldehyde

Question 153.
Fats on alkaline hydrolysis give …………
(a) Oil + Soap
(b) Soap + Glycol
(c) Soap + Ester
(d) Soap + Glycerol
Answer:
(d) Soap + Glycerol

Question 154.

B. in this reaction A and B are respectively
(a) Alkene, Alkyne
(b) Alkanal, Alkene
(c) Alkyne, Alkanal
(d) Alkyne, Alkene
Answer:
(b) Alkanal, Alkene

Question 155.
Oxygen atom in ether is …………
(a) very active
(b) replacable
(c) comparatively inert
(d) less active
Answer:
(c) comparatively inert

Question 156.
Chlorination of toluene in the presence of light and heat followed by treatment with aqueous NaOH gives ………….
(a) O – cresol
(b) P – cresol
(c) Phioroglucinol
(d) Benzyl alcohol
Answer:
(c) Phioroglucinol

Question 157.
Primary alcohols can be obtained from the reaction of RMgX with …………
(a) CO₂
(b) HCHO
(c) CH₃CHO
(d) H₂O
Answer:
(b) HCHO

Question 158.
The dehydration of alcohol is an example of ………….
(a) Bimolecular elimination reaction
(b) Nucleophilic substitution reaction
(c) Unimolecular elimination reaction
(d) internal substitution reaction
Answer:
(c) Unimolecular elimination reaction

Question 159.
Ethanol is converted into Ethoxy ethane ………….
(a) by heating with cone. H₂SO₄ at 443 K
(b) by heating with conc. H₂SO₄ at 413 K
(c) by heating with excess oxygen
(d) by heating with hydrogen
Answer:
(b) by heating with conc. H₂SO₄ at 413 K

Question 160.
Which of the following is not the product of dehydration of


Answer:

II. Fill in the blanks

1. Cholesteryl alcohol commonly known as …………. is an important component in our ………….
2. …………. the storage form of vitamin A, finds application in proper functioning of our eyes.
3. Methanol s used as an …………. solvent.
4. Isopropyl alcohol is used as …………. for injection.
5. CH₂CHOH is called as ………….
6. An example of hexahydric alcohol is ………….
7. The IUPAC name of glycerol is ………….
8. The TUPAC name of Neopentyl alcohol is ………….
9. The TUPAC name of CH₂ CH – CHOH is ………….
10. In methanol, the – OH group attached to …………. hybridised carbon atom.
11. The bond angle C – OH in methanol is ………….
12. alkyl halides undergo substitution by SN² reaction whereas …………. and …………. alkyl halides undergo substitution by SN¹ reaction.
13. Addition of H₂O to an unsymmetric alkene in the process of sulphuric acid follows ………….
14. Nucleophilic addition of Grignard reagent to aldehydes/ketones take place in the presence …………. followed by acid hydrolysis gives .
15. With RMgx …………., …………. gives l°alcohol.
16. Butyl Magnesium bromide reacts with propanone to give ………….
17. …………. is used to prepare a secondary alcohol with identical group.
18. Hydroboration yields an …………. product.
19. …………. is the best reagent to prepare unsaturated alcohol by reduction reaction of carbonyl compound.
20. …………. occurs in natural fats and in long chain fatty acids in form of triglycerides.
21. The alkaline hydrolysis of fats gives glycerol and the reaction is known as ………….
22. In Lucas test …………. alcohol do not react at room temperature.
23. In Victor Meyer’s test no colouration will be observed in case of ………….
24. Alkyl halide formation from primary alcohol follows …………. mechanism.
25. Alkyl halide formation from tertiary alcohol follows …………. mechanism.
26. The reaction between methanol and thionyl chloride in the presence of pyridine follows…………. mechanism.
27. …………. alcohols undergo dehydration by E₂ mechanism whereas alcohols undergo dehydration by E₁ mechanism.
28. To stop the oxidation reaction of alcohol at aldehyde / ketone stage …………. is used as an oxidising agent.
29.  In …………. oxidation dimethyl sulfoxide (DMSO) is used as an oxidising agent.
30. The fermentation of food consumed by an animal produces …………..
31. The detoxify the alcohol, the liver produces an enzyme called ………….
32. …………. present in the animals act as an oxidising agent and …………. catalyses the oxidation of toxic alcohol into non-toxic aldehydes.
33. Ethylene glycol, when heated to 773 K, it forms ………….
34. The reagent used to convert ethane 1, 2 -diol to ethanal is ………….
35. When Ethane – 1, 2 -diol is treated with conc.H₂S0₄, it forms ………….
36. The intermediate product formed when ethylene glycol is treated with periodic acid is ………….
37. The final product formed when glycol reacts with periodic acid is ………….
38. The IUPAC name of Acrolein (or) CH₂ = CH – CHO is ………….
39. Oxidation of glycerol with dilute nitric acid gives …………. and ………….
40. Oxidation of glycerol with bismuth nitrate gives ………….
41. Oxidation of glycerol with Fenton’s reagent gives ………….
42. LTA is known as ………….
43. Oxidation of glycerol with acidified KMnO₄ gives ………….
44. FeSO₄ + H₂O₂ is called ………….
45. …………. is used as a substitute for petrol under the name and used as fuel for aeroplane.
46. …………. is used as an anti-freezer in automobile radiators.
47. …………. is used as a sweetening agent in confectionery and beverages.
48. …………. is used in the manufacture of transparent soap, printing ink and stamp pad ink.
49. Glycerol is used in the manufacture of explosives like and by mixing with ………….
50. Except …………. all other alcohols are weaker acid than water.
51. The electron withdrawing groups such as – NO₂, – Cl enhances the acidic nature of phenol especially when they are present at …………. positions.
52. The LUPAC name of hydroxy quinol is ………….
53. The IUPAC name of orcinol is ………….
54. The other name of 1, 2, 3 – trihydroxy benzene is ………….
55. The reaction of chioro benzene with aqueous NaOH to give phenol is known as ………….
56. The product formed when benzene diazonium chloride is boiled with hot water is ………….
57. The IUPAC name of curnene is ………….
58. Phenol is converted to benzene on heating with ………….
59. The acetylation and benzoylation of phenol are called ………….
60. The reagent used in the conversion of phenol to 1, 4 – benzo quinone is ………….
61. When phenol is treated with Conc.HNO₃ and Conc.H₂SO₄, the product formed is ………….
62. Phenol reacts with bromine water to give a precipitate of ………….
63. The conversion reaction of phenol to salicylic acid is known as ………….
64. The conversion reaction of phenol into salicylaldehyde is known as ………….
65. The product formed when phenol is treated with phthalic anhydride in the presence of Conc.H₂SO₄ is ………….
66. …………. dye is Ibmied when phenol couples with benzene diazonium chloride in an alkalin
    solution.
67. Phenol gives …………. colouration with neutral FeCI₃.
68. Phenol formaldehyde is known as ………….
69. The IUPAC name of tertiary butyl methyL ether is known as ………….
70. C₆H₅O – CH₂ – CH₃ is known as ………….
71. The mechanism take place when alkyl halide is treated with alcohol solution of sodiunalkoxide is ………….
72. The dipole moment of diethyl ether is ………….
73. The reaction take place when ethers are exposed to oxygen is ………….
74. …………. is used as a surgical anesthetic agent in surgery.
75. …………. is used as refrigerant.

Answer:

1. cholesteroL, cell membrane
2. Retinol
3. industrial
4. skin cleanser
5. vinyl alcohol (or) ethenol
6. Sorbitol
7. propan – 1, 2, 3 – tnol,
8.  2, 2 – ditnethyl propan – 1 – ol
9. prop – 2 – en – 1 – ol
10. sp³
11. 108.9°
12. 1°, 2°, 3°
13. Markownikoff’s rule
14. dry ether, alcohol
15. formaldehyde, HCHO
16. 2-methyl hexan – 2 – ol
17. Formate ester
18. Anti-Markownikoft’s
19. LiAlH₄
20. Glycerol
21. Saoinufucatuib
22. Primary
23. Tertiary alcohol
24. SN²
25. SN¹
26. SN²
27. Pnmary, Tertiary
28. pyridinium chlorochromate
29. Swer
30. alcohol
31. alcohol dehydrogenase ALH
32. NAD,ADH
33. epoxide (or) 1,2-epoxy ethane (or) oxirane
34. dil.H₂SO (or) anhydrous ZnCI₂
35. 1,4 – dioxane
36. cyclic periodate ester
37. formaldehyde
38. prop – 2 – enal
39. glycenc acid, Tartronic acid
40. Meso oxalic acid
41. glycerose (or) a mixture of glyceraldehyde and dihydroxy acetone
42. Lead tetra acetate
43. Oxalic acid
44. 44. Fenton’s reagent
45. Ethanol, Power alcohol
46. Ethylene glycol
47. Glycerol
48. Glycerol
49. dynamite, cordite, china clay
50. Methanol
51. ortho and para
52. 1, 2, 4 – trihydroxy benzene
53. 3, 5 – dihydroxy toluene
54. Pyrogallol
55. Dows process
56. Phenol
57. 2 – phenyl propane
58. Zinc dust
59. Schotten-Baumann reaction
60. acidified K₂Cr₂O₇
61. 2,4, 6 – trinitro phenol (or) Picric acid
62. white, 2,4, 6-tribromo phenol
63. Kolbe’s Schmitt reaction
64. Riemer-Tiemann Reaction
65. Phenol phthalein
66. P-hydroxy azo benzene (or) Red orange dye
67. Purple
68. Bakelite
69. 2-methoxy – 2 – methyl propane
70. Phenatole (or) Ethoxy benzene
71. SN²
72. 1.18 D
73. auto oxidation
74. Diethyl ether
75. Diethyl ether

III. Match the following Colum – I with Column – II ysubg tge cide guveb below.

Question 1.

Answer:
(a) 3 4 1 2

Question 2.

Answer:
(a) 2 4 1 3

Question 3.

Answer:
(c) 4 3 2 1

Question 4.

Answer:
(a) 3 1 4 2

Question 5.

Answer:
(b) 4 3 1 2

Question 6.

Answer:
(a) 3 1 4 2

Question 7.

Answer:
(a) 3 1 4 2

Question 8.

Answer:
(a) 2 3 4 1

Question 9.

Answer:
(a) 3 4 1 2

Question 10.

Answer:
(a) 2 3 4 1

Question 11.

Answer:
(a) 3 1 4 2

Question 12.

Answer:
(a) 2 3 4 1

Question 13.

Answer:
(a) 2 3 4 1

Question 14.

Answer:
(a) 4 1 2 3

Question 15.

Answer:
(a) 3 1 4 2

Question 16.

Answer:
(a) 4 1 2 3

Question 17.

Answer:
(a) 4 3 1 2

IV. Assertion and reasons.

Question 1.
Assertion(A): P – nitro phenol is having lower pK_a value than phenol.
Reason (R): The electron with drawing group – NO₂ at para position enhances the acidic nature.
(a) Both A and R are correct and R is the correct explanation of A.
(b)BothAand Rare wrong
(c) A is wrong but R is correct
(d) A is correct but R is wrong
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 2.
Assertion(A): Alcohols cannot be used as solvent for Grignard reagent.
Reason (R): Alcohols are decomposed by Grignard reagents to give alkane.
(a) Both A and R are correct and R is the correct explanation of A.
(b) A is correct but R is wrong
(c) A is wrong but R is correct
(d) Both A and R are correct but R is not correct explanation of A.
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 3.
Assertion(A): Phenols are soluble in alcohols.
Reason (R): Phenols are soluble in alcohol due to the formation of inter molecular hydrogen bonding.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and R are wrong .
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 4.
Assertion(A): Phenol is insoluble in NaHCO₃ solution but acetic acid is soluble.
Reason (R): Phenols are weakly acidic and hence they dissolve only in strong base and insoluble in weak base like NaHCO₃. But acetic acid is a stronger acid than phenol and so it is soluble in weak base NaHCO₃.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and are correct
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 5.
Assertion(A): Glycol is more viscous than ethanol.
Reason (R): Glycol contains two hydroxyl groups and the inter molecular hydrogen bonding is made much stronger resulting in a polymeric structure. This leads to high viscosity than ethanol.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and are correct but R is not the correct explanation of A.
(c) Both A and R are wrong
(d) A is correct but R is wrong
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 6.
Assertion(A): Ethanol is a weaker acid than Phenol.
Reason (R): Sodium ethoxidc may be prepared by the reaction of ethanol with sodium metal but phenol reacts with NaOH.
(a) Both A and R are correct and R ¡s the correct explanation of A
(b) Both A and R are correct but R is not the correct explanation of A
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R ¡s the correct explanation of A

Question 7.
Assertion(A): Both alcohol and ether have higher boiling point.
Reason (R): Both are having intermolecular hydrogen bonding.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and R are wrong
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(b) Both A and R are wrong

Question 8.
Assertion(A): Bond angle in ethers is slightly less than the tetra hedral angle.
Reason (R): There is a repulsion between the two bulkier R groups.
(a) Both A and R are correct but R is not the correct explanation of A.
(b) Both A and arc wrong
(c) Both A and R are correct and R is the correct explanation of A.
(d) A is correct but R is wrong
Answer:
(c) Both A and R are correct and R is the correct explanation of A.

Question 9.
Assertion(A): P-nitro phenol is a stronger acid than o – nitro phenol.
Reason (R): Intra molecular hydrogen bonding in o – nitro phenol make it as a weaker acid.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and are wrong
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 10.
Assertion(A): Phenol is more reactive towards electrophilic substitution reaction.
Reason (R): In the case of phenol, the intermediate carbo cations is more resonance stabilized.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and are wrong
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 11.
Assertion(A): Phenol forms 2, 4, 6 – tribromo phenol on treatment with Br₂ in CS₂ at 273 K.
Reason (R): Bromine polarizes in CS₂.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and are incorrect
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(b) Both A and are incorrect

Question 12.
Assertion(A): Phenol is more acidic than ethanol.
Reason (R): Phenoxide ion is more stable than ethoxide due to resonance.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and R are correct but R is not the correct explanation of A.
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 13.
Assertion(A): Boiling point of ethanol is higher in comparison to methoxy methane.
Reason (R): Ethanol is associated with inter molecular hydroxide bonding whereas in methoxy methane, inter molecular hydrogen bonding is not present.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and R are correct but R is not the correct explanation of A.
(c) Both A and R are not correct
(d) A is correct but R is wrong
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 14.
Assertion(A): (CH₃)₃ C – O – CH₃ on reaction with HI gives CH₃OH and (CH₃)₃C – I as the main products and not (CH₃)₃ C – OH and CH₃I.
Reason (R): (CH₃)₃ C + (Tertiary carbo cation) is more stable and reacts with HI to form (CH₃)₃ C – I as main product.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and are wrong
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 15.
Assertion(A): The bond angle (C – O – H) in methanol is reduced to 108.9° from the regular tetra hedral bond angle of 109.5°.
Reason (R): In methanol, two lone pairs of electrons are present in oxygen atom and due to lone pair – lone pair repulsion, the bond angle is reduced.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and R are correct but R is not the correct explanation of A.
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 16.
Assertion(A): LiAlH₄ is the best reagent to prepare unsaturated alcohols from carbonyl compounds.
Reason (R): LiAlH₄ does not reduce the carbon – carbon double bond present in the carbonyl carbon compound.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and R are correct but R is not the correct explanation of A.
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 17.
Assertion(A): Primary alcohols are more acidic than tertiary alcohol.
Reason (R): Alkyl groups (electron releasing group) increases the electron density on oxygen and decreases the polar nature of – OH bond. Hence it results in the decrease in acidity.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and R are not correct
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 18.
Assertion(A): P – cresol is less acidic than phenol.
Reason (R): Alkyl substituted phenols show a decreased acidity due to the electron releasing + I effect of alkyl group.
(a) Both A and R are correct but R is not the correct explanation of A.
(b) Both A and R are correct and R is the correct explanation of A.
(c) Both A and R are wrong
(d) A is correct but R is wrong
Answer:
(b) Both A and R are correct and R is the correct explanation of A.

Question 19.
Assertion(A): O – nitro phenol is slightly soluble in water whereas P – nitro phenol is more soluble in water.
Reason (R): O – nitro phenol has intra molecular hydrogen bonding whereas P – nitro phenol has inter molecular hydrogen bonding.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and are wrong
(c) A is correct but R is wrong
(d) A is wiong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Question 20.
Assertion(A): Inter molecular dehydration of alcohol is not a suitable method of prepare mixed ethers.
Reason (R): When a mixture of two different alcohols are used, mixture of different ethers are formed and they are difficult to separate.
(a) Both A and R are correct and R is the correct explanation of A.
(b) Both A and R are correct but R is not the correct explanation of A.
(c) A is correct but R is wrong
(d) A is wrong but R is correct
Answer:
(a) Both A and R are correct and R is the correct explanation of A.

Samacheer Kalvi 12th Chemistry Hydroxy Compounds and Ethers 2 Mark Questions and Answers

V. Answer the following

Question 1.
Write the molecular formula and IUPAC name of the following compounds.

1. Vinyl alcohol
2. Sorbitol

Answer:
1. Vinyl alcohol
CH₂ = CHOH
IUPAC name: Ethenol

2. Sorbitol
HO – CH₂ – (CHOH)₄ – CH₂OH
IUPAC name : Hexan – 1, 2, 3, 4, 5, 6 – hexol

Question 2.
Write the structural formula of the following compounds.

1. Prop – 2 – en – 1 – ol
2. Prop – 3 – en – 1 – ol

Answer:
1. Prop – 2 – en – 1 – ol : CH₂ = CH – CH₂OH

2. Prop – 3 – en – 1 – oI :

Question 3.
Write the structural formula of the following compound.

1. Phenyl methanol
2. 2 – methyl – but – 3 – en – 2 – ol

Answer:
1. Phenyl methanol : C₆H₅ – CH₂OH

2. 2 – methyl – but – 3 – en – 2 – ol :

Question 4.
Write the possible isomers for the formula

1. C₂H₆O
2. C₃H₈O

Answer:
1. C₂H₆O

2. C₃H₈O
(a) CH₃ CH₂ – CH₂ OH : Propan – 1 – ol

(b)
Propan – 1 – ol

(a) and (b) – Position isomerism
(a) and (c) – Functional isomerism

Question 5.
Explain about the structure of methanol.
Answer:
1. In methanol, one of the sp³ hybridised orbital of oxygen linearly overlap with the sp³ hybridised orbital of carbon to form a C – O, a bond and another sp³ hybridised orbitai linearly overlap with 1s orbital of hydrogen atom to form a O – H a bond.

2.

3. The remaining two sp3 hybridised orbitais of oxygen are occupied by two lone pairs of electrons. Due to the lone pair – lone pair repulsion, the C – O – H bond angle in methanol is reduced to 108.9° from the regular tetrahedral bond angle of 109.5°.

Question 6.
Convert phenyl magnesium bromide to phenyl methanol (or) How would you prepare phenyl methanol from Grignard reagent?
Answer:

Question 7.
How will you prepare Butan-2-ol from ethanal? (or) Convert Ethyl Magnesium bromide into 2 – Butanol (or) Starting from acetaldehyde, how would you obtain butan – 2 – ol?
Answer:

Question 8.
Convert propanone into 2 – methyl – propan – 2 – ol.
Answer:

Question 9.
Starting from butyl magnesium bromide, how would you obtain 2 – methyl bexan – 2 – ol?
Answer:

Question 10.
What happens when methyl magnesium bromide reacts with ethl methanoate followed by acid hydrolysis?
Answer:

Question 11.
LiAlH₄ is a best reagent to prepare unsaturated alcohol. Prove it.
Answer:
LiAIH₄(Lithium Aluminium Hydride) does not reduce the carbon – carbon double bond present in the carbonyl compound and hence it is the best reagent to prepare unsaturated alcohol.

Question 12.
Convert acetone into propan – 2 – ol.
Answer:

Question 13.
How would you get Benzyl alcohol from Benzoic acid.
Answer:

Question 14.
Starting from ethyl ethanoate, how would you prepare ethanol?
Answer:

Question 15.
How will you prepare 4 – alkyl – 4 – hydroxy butanoic acid?
Answer:
When two or more functional groups are present in a molecule a less vigorous sodium borohydride is used as a reducing agent to reduce the more reactive group. For example, if a compound contains both carbonyl and carboxyl group, NaBH₄ reduces the carbonyl group.

Question 16.
What is saponification? Explain with equation.
Answer:
The alkaline hydrolysis of fats gives glycerol and soap then the reaction is known as saponification.

Question 17.
What happens when thionyl chloride is treated with methanol?

The above reaction follows SN² mechanism in the presence of pyridine.

Question 18.
Answer:
1. In Swern oxidation method, dimethyl sulfoxide (DMSO) is used as the oxidising agent and it converts alcohols to ketones / aldehydes.

2. When propan – 2 – ol is treated with DMSO and oxalyl chloride followed by the addition of triethylamine, it produces Propanone.

Question 19.
Explain biological oxidation with an example.
Answer:
Biological oxidation is the fermentation of the food consumed by an animal produces alcohol. To detoxify the alcohol, the liver produces an enzyme called alcohol dehydrogenase (ADH). Nicotinamide adenine dinucleotide (NAD) present in the animals acts as a oxidising agent and ADH catalyses the oxidation of toxic alcohols into non-toxic aldehyde.

Question 20.
What is esterificatloin? Explain with equation.
Answer:
Alcohols react with carboxylic acids in the presence of an acid to give esters. This reaction is known as Esterification.

Question 21.
How would you convert ethylene glycol into ethene?
Answer:

Question 22.
Explain the action of conc.HNO₃ and conc.H₂SO₄ with ethan – 1, 2 – diol.
Answer:

Question 23.
What happens when ethylene glycol is treated with periodic acid?
Answer:
Ethylene glycol on treatment with periodic acid gives formaldehyde. This reaction is selective for vicinal 1, 2 – diols and it proceeds through a cyclic periodate ester intermediate.

Question 24.
How is glycerol reacts with fuming nitric acid? (or) How would you convert glycerol into nitroglycerine?
Answer:

Question 25.
What happens when conc.H₂SO₄ or KHSO₄ is heated with glycerol?
Answer:
Dehydration:

Question 26.
Mention the uses of methanol.
Answer:

1. Methanol is used as a solvent for paints, varnishes, shellac, gums, cement, etc.
2. Methanol is used in the manufacture of dyes, drugs, perfumes and formaldehyde.

Question 27.
What are the uses of ethylene glycol?
Answer:

1. Ethylene glycol is used as an antifreeze in automobile radiator
2. Its dinitrate is used as an explosive with DNG.

Question 28.
Write a note about acidity of aliphatic alcohols.
Answer:
1. According to Bronsted theory, an acid is defined as a proton donor and the acid strength is the tendency to give up a proton. Alcohols are similarly acidic when compared with water. Except methanol, all other alcohols are weaker acid than water. The K_a value for water is 1.8 x 10^-16 where as for alcohols the Ka value in the order 10^-18 to 10^-16.

2. 2C₂H₅ – OH + 2Na → 2C₂H₅ONa + H₂ ↑
This reaction explains the acidic nature of alcohol as it liberates H₂ gas with Na metal.

Question 29.
Alcohol can act as Bronsted base. Prove this statement.
Answer:
Alcohols can also act as a Bronsted bases. It is due to the presence of unshared electron pairs on oxygen which make them to accept proton. So proton acceptor are Bronsted bases. i.e., alcohols are Bronsted bases.

Question 30.
What are cresols? Give examples.
Answer:
Methyl Phenols are called cresols.
They are

Question 31.
How is phenol obtained from benzene suiphonic acid?
Answer:

Question 32.
How is Aniline converted into Phenol?
Answer:
Aniline is diazotized with nitrous acid (NaNO₂ + HCI ) at 273 – 278K to give benzene diazonium chloride which on further treatment with hot water in the presence of mineral acid gives phenol.

Question 33.
How will you convert phenol into benzene?
Answer:
Phenol is converted to benzene on heating with Zinc dust.

Question 34.
What happens when phenol is heated with NH₃?
Answer:

Question 35.
What happens when phenol is heated with acidified K₂Cr₂O₇?
Answer:

Question 36.
How is phenol treated with Nickel?
Answer:

Question 37.
O – nitro phenol is slightly soluble ¡n water where as P-nitro phenol is more soluble. Cive reason.
Answer:
O-nitro phenol is slightly soluble in water and more volatile due to intra molecular hydrogen bonding, whereas P-nitro phenol is more soluble in water and less volatile due to intermolecular hydrogen bonding.

Question 38.
Explain Reimer Tiemann reaction.
Answer:
On treating phenol with CHCl₃ / NaOH, a – CHO group is introduced at ortho position. This reaction proceeds through the formation of substituted benzal chloride intermediate.

Question 39.
How is phenolphthalein prepared from phenol?
Answer:
On heating phenol with phthalic anhydride in presence of con.H₂SO₄, phenolphthalein is obtained,

Question 40.
What is Coupling reaction? Give equation.
Answer:
Phenol couples with benzene diazonium chloride in an alkaline solution to form p-hydroxy azobenzene(a red orange dye).

Question 41.
Write a note about the structure of ethereal oxygen.
Answer:
The structure of ethereal oxygen which is attached to two alkyl groups is similar to the structure of – OH group of alcohol. The oxygen atom is sp³ hybridized. Two sp³ hybridized orbitals of oxygen linearly overlap with two sp³ hybrid orbitais of the carbon which are directly attached to the oxygen forming two
C – O ‘σ’ bonds.

The C – O – C bond angle is slightly greater than the tetrahedral bond angle due to the repulsive interaction between the two bulkier alkyl groups.

Question 42.
Write the structure and common name of

1. Ethoxy benzene
2. Phenoxy benzene

Answer:
1. C₆H₅ – O – CH₂ – CH₃ : Ethoxy benzene (or) Phenetole (or) Ethyl phenyl ether

2. C₆H₅ – O – C₆H₅ : Phenoxy benzene (or) Diphenyl ether (or) Phenyl ether

Question 43.
What happens when ethanol reacts with conc. H₂SO₄ Sulphuric acid at 413 K?
Answer:
When ethanol reacts with con.H₂SO₄ at 413 K, inter molecular dehydration take place and diethyl ether is formed as product.

Question 44.
Explain the action of diazomethane with ethanol.
Answer:
Methyl ethers can be prepared when ethanol is treated with diazomethane in presence of fluoro boric acid.

Question 45.
Ether are miscible with water. Justify this statement.
Answer:
1. Oxygen of ether can also form Hydrogen bond with water and hence they are miscible with water.

2. Ethers dissolve wide range of polar and non-polar substances.

Question 46.
Ether bottle should not be kept open. Why?
Answer:
1. When ether bottle is kept open, they are exposed to atmospheric oxygen and slowly oxidised to form hydroperoxides and dialkyl peroxides. These are explosive in nature. Such a spontaneous oxidation by atmospheric oxygen is called autooxidation.

Question 47.
Explain the action of hydrogen iodide with anisole (or) methoxy benzene. –
Answer:

Question 48.
What are the uses of anisole?
Answer:

1. Anisole is a precursor to the synthesis of perfumes and insecticide pheromones,
2. It is used as a pharmaceutical agent.

Question 49.
Alcohols are comparatively more soluble in water than hydrocarbons of comparable molecular masses. Explain this fact.
Answer:
Alcohols can form H-bond with water molecules and break the H-bond already existing between the water molecules. Therefore, they are soluble in water.

On the other hand hydrocarbons do not have the ability to form H-bond with water molecules. Hence they are insoluble in water.

Question 50.
Explain why is ortho nitrophenol more acidic than ortho methoxyphenol?
Answer:
Ortho nitrophenol is more acidic than ortho methoxyphenol because nitro group is an electron withdrawing and it will increase +ve charge on the oxygen atom to make it more acidic whereas – OCH₃ group is an electron releasing group and it will decrease +ve charge on the oxygen atom, thus making it less acidic and hence the O – H bond will not break easily.

Question 51.
Give reason for the higher boiling point of ethanol in comparison to methoxymethane.
Answer:
Ethanol undergoes intermolecular H-bonding due to the presence of a hydrogen atom attached to the electronegative oxygen atom. As a result, ethanol exists as associated molecules.

Consequently, a large amount of energy is required to break these hydrogen bonds. Therefore, the boiling point of ethanol is higher than that of methoxymethane which does not form H-bonds.

Question 52.
What happens when phenol is treated with ¡ce cold bromine dissolved in CS₂?
Answer:

Question 53.
What happens when phenol is treated with excess of nitrating mixture? (Give equation only).
Answer:

Question 54.
Describe the mechanism by which the hydroxyl group attached to an aromatic ring is more acidic than the hydroxyl group attached to an alkyl group. How does the presence of nitro group in phenol affects its acidic character?
Answer:
1. The reaction of phenol with aqueous sodium hydroxide solution indicates that phenol is a stronger acid than alcohols in water.

2. Because phenoxide ion formed is stabilised by resonance whereas alkoxide ion formed is destabilised by positive inductive effect of alkyl group.

3. Presence of electron withdrawing group such as nitro group enhances the acidic strength of phenol. lt is due to the effective delocalisation of the negative charge in phenoxide ion.

Question 55.
Give two reactions that show the acidic nature of phenol. Compare the acidity of phenol with that of ethanol.
Answer:

Samacheer Kalvi 12th Chemistry Hydroxy Compounds and Ethers 3 Mark Questions and Answers

VI. Answer the following questions.

Question 1.
Give one example for each of the following with their structure and IUPAC name.

1. 1° alcohol
2. 2° alcohol
3. 3° alcohol

Answer:

Question 2.
Write the structure of the following compounds.

1. Phenyl methanol
2. 1 – Phenyl ethanol
3. 2 – Phenyl propan – 2 – ol

Answer:

Question 3.
Write the structures and IUPAC names of the following compounds.

1. Tertiary butyl alcohol
2. Neopentyl alcohol
3. Isobutyl alcohol

Answer:
1.
2 – methyl propan – 2 – ol (Tertiary butyl alcohol)

2.
2, 2 – dimethyl propan – 1 – ol (Neopentyl alcohol)

3.
2 – methyl propan – 1- ol (Isobutyl alcohol)

Question 4.
Draw the structures and write the IUPAC name of the following compounds.

1. Benzyl alcohol
2. Allyl alcohol
3. Cyclohexyl alcohol

Answer:
1.
Phenyl methanol (Benzyl alcohol)

2. CH₂ = CH – CH₂OH  Prop – 2 – en – 1 – ol (Allyl alcohol)

3.
Cyclo hexanol (Cyclohexyl alcohol)

Question 5.
Describe Lucas test used to distinguish Primary, Secondary and Tertiary alcohols.
Answer:
When alcohols are treated with Lucas agent (conc. HCI + anhydrous ZnCl₂) at room temperature, tertiary alcohols react immediately to form a turbidity due to the formation of alkyl chloride which is insoluble in the medium. Secondary alcohols react within 10 minutes to form a turbidity of alkyl chloride where primary alcohols do not react at room temperature.

Question 6.
Explain the mechanism of the reaction of alkyl halide formation from primary alcohol.
Answer:

Question 7.
Explain SN¹ mechanism of Tertiary alcohols reaction with HBr.
Answer:

Question 8.
Explain the mechanism involved in the reaction of phosphorous trichloride with Ethanol. SN² reaction of Ethanol with PCl₃
Answer:

Question 9.
Describe Saytzeff’s rule with example.
Answer:
1. During intramolecular dehydration, if there is a possibility to form a carbon – carbon double bond at different locations, the preferred location is the one that gives the more (highly) substituted alkene i.e., the stable alkene.

2. For example, the dehydration of 3, 3 – dimethyl – 2 – butanol gives a mixture of alkenes. The secondary carbocation formed in this reaction undergoes rearrangement to form a more stable tertiary carbocation.

Question 10.
Explain the following reactions.

Answer:

Question 11.
Explain about catalytic dehydrogenation of 1⁰, 2⁰ and 3⁰ alcohols
Answer:

Question 12.
Describe about the oxidation reaction of ethylene glycol with dilute nitric acid.
Answer:
When dilute nitric acid (or) alkaline KMnO₄ is used as the oxidizing agent, the following products are formed.

Question 13.
Explain about the oxidation reaction of Glycerol with different oxidising reagents.
Answer:

1. Oxidation of glycerol with dii. FINO₃ gives glyceric acid and tartronic acid.
2. Oxidation of glycerol with Conc. HNO₃ gives mainly glyceric acid.
3. Oxidation of glycerol with bismuth nitrate gives as meso oxalic acid.
4. Oxidation of glycerol with Br₂ /H₂O (or) NaOBr (or) Fenton reagent (FeSO₄ + H₂O₂)
5. gives a mixture of glyceraldehyde and dihydroxy acetone(glycerose).
6. On oxidation with HIO₄ or Lead tetra acetate (LTA) it gives formaldehyde and formic acid.
7. Acidified KMnO₄ oxidises glycerol into oxalicacid.

Question 14.
What are the uses of ethanol.
Answer:

1. Ethanol is used as an important beverage.
2. It is also used in the preparation of
   • Paints and varnishes
   • Organic compounds like ether, chloroform, iodoform, etc.,
   • Dyes, transparent soaps.
3. As a substitute for petrol under the name power alcohol used as fuel for aeroplane.
4. It is used as a preservative for biological specimens.

Question 15.
Mention the uses of Glycerol.
Answer:

1. Glycerol is used as a sweetening agent in confectionery and beverages.
2. It is used in the manufacture of cosmetics and transparent soaps.
3. It is used in making printing inks and stamp pad ink and lubricant for watches and clocks.
4. It is used in the manufacture of explosive like dynamite and cordite by mixing it with china clay.

Question 16.
Compare the acidity of 1°, 2° and 3° alcohols.
Answer:
1. The acidic nature of the alcohol is due to the polar nature of O – H bond. When an electron withdrawing -I groups such as – Cl, – F etc… is attached to the carbon bearing the OH group, it withdraws the electron density towards itself and thereby facilitating the proton donation.

2. In contrast, the electron releasing group such as alkyl group increases the electron density on oxygen and decreases the polar nature of 0 – H bond, I lence it results in the decrease in acidity.

3. On moving from primary to secondary and tertiary alcohols, the number of alkyl groups which attached to the carbon bearing -OH group increases, which results in the following order of acidity.
1°alcohol > 2° alcohol > 3° >alcohol

For example

Question 17.
What are dihydric phenols? Give three examples.
Answer:
When benzene ring has 2 – OH groups, it is called Dihydric phenol.

Question 18.
What are Trihydric phenols. Give example.
Answer:
When 3 – OH groups are present in benzene ring, it is called trihydric phenol.

Question 19.
Write the possible isomers for the formula C₇H₈O with their names C₇H₈O
Answer:
1. C₆H₅ – CH₂OH : Benzyl alcohol

2. C₆H₅ – O – CH₃ : Anisole

3.

4.

5.

Question 20.
Explain about the bromination of phenol.
Answer:
1. Phenol reacts with bromine water to give a white precipitate of 2, 4, 6 – tri bromo phenol.

2. When phenol reacts with Br₂ in the presence of CS₂ or CCl₄ at 278K. a mixture of ortho and para bromo phenols are formed.

Question 21.
Differentiate phenols from alcohol.
Answer:
Test to differentiate alcohols and phenols:
1. Phenol react with benzene diazonium chloride to form a red orange dye, but ethanol has no reaction with it.

2. Phenol gives purple colouration with neutral feme chloride solution, alcohols do not give such coloration with FeCI₃.

3. Phenol reacts with NaOH to give sodium phenoxide. Ethyl alcohol does not react with NaOH

Question 22.
What are the uses of phenol?
Answer:

1. About half of world production of phenol is used for making phenol formaldehyde resin. (Bakel ite).
2. Phenol is a starting material for the preparation of
   • drugs such as phenacetin, Salol, aspirin, etc.
   • phenolphthalein indicator.
   • explosive like picric acid.
3. It is used as an antiseptic – carbolic lotion and carbolic soaps.

Question 23.
Write the structure formula and IUPAC name of the following.

1. n – heptyl phenyl ether
2. Isopentyl phenyl ether
3. Dimethyl glycolate

Answer:

Question 24.
ExplaIn about the mechanism of intermolecular dehydration of ethanol with conc.H₂SO₄ at 413 K.
Answer:
When ethanol reacts with conc.H₂SO₄ at 413 K, inter molecular dehydration takes place and the product formed is Ethoxy ethane.
Mechanism:

Question 25.
Explain about the mechanism involved in Williamson’s synthesis.
Answer:
When an alkyl halide is heated with an alcoholic solution of sodium alkoxide, the corresponding ether is formed. This reaction involves SN² mechanism.

Mechanism:

Question 26.
Explain the mechanism involved in the reaction between Tertiary alkyl halide and primary alkoxide with eample.
Answer:
When tertiary alkyl halide reacts with primary alkoxide, elimination dominates and succeeds over substitution to form an alkene.

Question 27.
Explain about the reaction mechanism of methoxy ethane with HI.
Answer:
Ethers can undergo nucleophilic substitútion reactions with HI.

Ethers having primary alkyl group undergo SN² reaction whereas tertiary alkyl ether undergo SN¹ reaction. Protonation of ether is followed by the attack of halide ion. The halide ion preferentially attacks the less sterically hindered of the two alkyl groups which are attached etherial oxygen.

Question 28.
What are the uses of diethyl ether.
Answer:

1. Diethyl ether is used as a surgical anesthetic agent in surgery.
2. It is a good solvent for organic reactions and extraction.
3. It is used as a volatile starting fluid for diesel and gasoline engine.
4. It is used as a refrigerant.

Question 29.
Classify the following as primary secondary and tertiary alcohols.

Answer:
Primary alcohols:

Secondary alcohols:

Tertiary alcohols:

Question 30.
Name the following compounds according to IUPAC system.

Answer:

Question 31.
Show how are the following alcohols prepared by the reaction of a suitable Grignard reagent on methanal?

Answer:

Question 32.
You are given benzene, conc H₂SO₄ and NaOH. Write the equations for the preparation of phenol using these reagents.
Answer:

Question 33.
How will you convert ethanol to acetone ?
Answer:

Question 34.
How are the following conversions carried out?

1. Phenol to Toluene
2. Ethanol to 1, 1 – dichloroethane.

Answer:

Question 35.
How are the following conversions carried out ? (Write the reactions and conditions in each case):

1. Ethanol to 2 – propanol
2. Phenol to Acetophenone

Answer:

Samacheer Kalvi 12th Chemistry Hydroxy Compounds and Ethers 5 Mark Questions and Answers

II. Answer the following questions.

Question 1.
Explain Victor Meyer’s test used to distinguish 1°, 2° and 3° alcohols.
Answer:
Victor Meyer’s test :
This test is based on the behaviour of nitro alkanes formed by the three types of alcohols with nitrous acid and it consists of the following steps.

1. Alcohols are converted into alkyl iodide by treating with I₂/P.
2. Alkyl iodides so formed is then treated with AgNO₂ to form nitro alkane.
3. Nitro alkanes are finally treated with HNO₂ (mixture of NaNO₂/HCl) and the resultant solution is made alkaline with KOH.

Result:

1. Primary alcohol gives red colour
2. Secondary alcohol gives blue colour.
3. No colouration will be observed in tertiary alcohol.

1° alcohol:

2°alcohol:

3°alcohol:

Question 2.
Write the possible isomers for the formula C₄H₁₀O, write their IUPAC names and structures.
Answer:
C₄H₁₀O – 7 Isomers

Question 3.
Explain about mechanism involved in the dehydration of tertiary alcohols.
Answer:
Tertiary alcohols undergo dehydration by E₁ mechanism. It involves the formation of a carbocation.
Step 1:

Step 2:
Dissociation of oxonium ion to form a carbocation

Step 3:
Deprotonation of carbocation to form an alkene

Question 4.
Explain about the various dehydration reactions of ethylene glycol.
Answer:
Ethylene glycol undergoes dehydration reaction under different conditions to form different products.
1. When ethylene glycol is heated to 773K, it forms epoxides.

2. When heated with dilute sulphuric acid (or) anhydrous ZnCl₂ under pressure in a sealed tube, it gives acetaldehyde.

3. When distilled with Conc. H₂SO₄, glycol forms 1, 4 – dioxane

Question 5.
Explain the following reactions.

1. Schotten-Baumann reaction
2. Kolbe’s reaction
3. Reimer – Tiemann reaction

Answer:
1. Schotten – Baumann reaction:

2. Kolbe’s reaction:

3. Reimer – Tiemann reaction.

Question 6.
Describe the following electrophilic substitution reaction using phenol.

1. Nitrosation
2. Nitration
3. Sulphonation

Answer:
1. Nitrosation:
Phenol can be readily nitrosoated at low temperature with nitrous acid.

2. Nitration:
Phenol can be nitrated using 20% nitric acid at room temperature, a mixture of ortho and para nitro phenols are formed.

3. Phenol when treated with Conc.HNO₃ and Conc.H₂SO₄, picric acid is formed.

4. Sulphonation:
Phenol when reacts with Conc.H₂SO₄ at 280K, o – phenol suiphonic acid is formed as major product. But when the reaction is carried out at 313K, the major product is p – phenol suiphonic acid.

Question 7.
What happens when diethyl ether reacts with following reagents.

1. excess O₂
2. Cl₂ / light
3. PCI₅
4. dil.H₂SO₄ / H₂O
5. CH₂COCI /Anhydrous ZnCI₂.

Answer:
Auto – oxidation:

Question 8.
Explain the aromatic electrophilic substitution reactions of anisole with equations. Aromatic electrophilic substitution reactions:
Answer:
1. Halogenation:

2. Nitration.

3. Friedel Craft’s alkylation.

4. Friedel Craft’s acylation.

Question 9.
Starting from phenol, how would you prepare the following compounds.

1. Benzene
2. Aniline
3. Anisole
4. 1, 4, benzoqulnone
5. Cyclohexanol

Answer:

Question 10.
A compound ‘A’ with molecular formula C₄H₁₀O is unreactive towards sodium metal. it does not add Bromine water and does not react with NaHSO₃ solution. On refluxing ‘A’ with excess of HI, it gives ‘B’ which reacts with aqueous NaOH to form ‘C’. ‘C’ can be converted into ‘B’ by reacting with red P and I₃. ‘C, on treating with conc. H₂SO₄ forms ‘D’. ‘D’ decolounses bromine water. Identify A to D and write the reactions involved.
Answer:

‘A’ is not an alcohol therefore it does not react with sodium metal. ‘A’ is also not an aldehyde or a ketone as it does not react with NaHSO3. ‘A’ is not an unsaturated hydrocarbon as it does not add Br₂ (aq). So, it is likely to be a ether.

Question 11.
An organic compound (A) of molecular formula C₂H₆O on reaction with conc.H₂SO₄ at 443 K gives an unsaturated hydrocarbon (B). (B) on reaction with Baeyer’s reagent produces (C) of molecular formula C₂H₆O₂. (C) on reaction with anhydrous ZnCI₂ produces (D) of molecular formula C₂H₄O. (D) reduces Tollen’s reagent. Identify A, B, C and D and explain the reactions involved.
Answer:
1. An organic compound (A) reacts with Conc.H₂SO₄ at 443 K produces ethene by intermolecular dehydration. So, (A) is ethanol – CH₃CH₂OH.

2. Ethene on reaction with Baeyer’s reagent (cold, dilute alkaline KMnO₄) produces ethylene glycol as product (C).

3. Ethylene glycol on reaction with anhydrous ZnCI₂ dehydration and tautomerisation take place to give actaldehyde as product (D).

Question 12.
An organic compound (A) of molecular formula C₂H₆O liberates H₂ gas with metallic sodium and gives (B). (B) on reaction with methyl bromide produces (C) of molecular formula C₃H₈O. (C) on reaction with excess III produces (D) and (E). Identify A, B, C, D and E and explain the reactions involved.
Answer:
1. An organic compound (A) reacts with Na metal and liberates H₂ gas means it must be an alcohol. From the molecular formula it is identified as ethanol – CH₃ – CH₂OH (A).

2. Ethanol on reaction with Na metal to produce sodium ethoxide as (B) with liberation of H₂ gas.

3. Sodium ethoxide on reaction methyl bromide undergo Williamson’s synthesis to produce methoxy ethane as (C).

4. Methoxy ethane on reaction with excess HI will give Ethyl iodide and Methyl iodide as (D) and (E).

Question 13.
An organic compound (A) of molecular formula CH₄O on mild oxidation gives (B) of formula CH₂O that reduces tollen’s reagent. (B) on reaction with methyl magnesium bromide followed by acid hydrolysis will give (C) of molecular formula C₂H₆O which liberates H₂ gas with metallic sodium. Identify A, B, C and explain the reactions involved.
Answer:
1. (A) is identified from the molecular formula as methanol (CH₃OH).

2. CH₃OH – methanol on mild oxidation will give formaldehyde as (B). Aldehydes reduce Tollen’s reagent to silver mirror. So, (B) is HCHO (methanal)

3. Formaldehyde reacts with CH₃MgBr, followed by acid hydrolysis produces primary alcohol and (C) is identified from the formula as CH₃ – CH₂OH – Ethanol. Ethanol liberates H₂ gas with metallic sodium.

Question 14.
An organic compound (A) of molecular formula C₂H₆O reacts with metallic Na and liberates H₂ gas. (A) on mild oxidation with Cu at 573 K gives (B) of molecular formula C₂H₄O. (B) on reaction with methyl magnesium bromide followed by acid hydrolysis gives (C) of molecular formula C₃H₅O. (C) gives Blue colour in Victor Meyer’s test. (C) on mild oxidation with Cu at 573 K gives (D) of formula C₃H₆O. identify A, B, C, D and
explain the reactions.
Answer:
1. An organic compound (A) reacts with Na metal and liberates H₂ gas means it must be alcohol. From the molecular formula it is identified as Ethanol (CH₃ – CH₂OH).

2. Ethanol on oxidation with Cu at 573 K undergoes catalytic dehydrogenation and produces Acetaldehyde as product (B).

3. Acetaldehyde on reaction with CH₃MgBr followed by hydrolysis will give Isopropyl alcohol as (C).

4. Propan – 2 – ol is secondary alcohol and so it gives blue colour in Victor Meyer’s test. (C) on reaction with Cu at 573 K will give Propanone as (D).

Question 15.
An organic compound (A) of molecular formula C₃H₈O gives blue colour in Victor Meyer’s test. (A) on reaction with Cu at 573 K gives (B) which further reacts with Methyl magnesium bromide followed by acid hydrolysis yields (C) of molecular formula C₄H₁₀O. (C) on reaction with Cu at 573 K gives (D) of formula C4H8. Identify A, B, C, D and explain the reactions involved.
Answer:
1. An organic compound gives blue colour in Victor Meyer’s test means it must be a secondary alcohol. From the formula, it is identified as
Propan – 2- ol (A)

2. Propan – 2 – ol on reaction with Cu at 573 K gives Propanone as (B).

3. Propanone on treatment with CH₃MgBr followed by acid hydrolysis will yield Tertiary butyl alcohol (CH₃)₃C – OH as (C).

4. Tertiary butyl alcohol on reaction with copper at 573 K undergoes dehydration reaction to

Question 16.
An organic compound (A) of molecular formula C₃H₆ on reaction with Conc. H₂SO₄ and H₂O gives ClH₅O as (B) as a MarkownikoWs product. (B) on oxidation with Cu at 573 K gives (C) of formula C₃H₆O. (C) on reaction with CH₃MgBr followed by acid hydrolysis yields (D) as C₄H₁₀O which will not give any colour in Victor Meyer’s test. Identify A, B, C, D and explain the reactions involved.
Answer:
1. An organic compound (A) is identified from the molecular formula as CH₃ – CH = CH₂ propene.

2. Propene on hydrolysis in acid medium, Markownikoff’s rule is followed and the product formed is
Propan – 2- ol as (B)

3. Propan – 2 – ol on reaction with Cu at 573 K undergoes dehydrogenation reaction to produce Propanone as (C).

4. Propanone on reaction with CH₃MgBr followed by acid hydrolysis gives tertiary butyl alcohol (D). It will not give any colouration in Victor Meyer’s test.

Question 17.
An aromatic compound (A) of molecular formula C₆H₅Cl on reaction with aqueous NaOH gives (B) of formula C6H60 that give violet colouration with neutral FeCI₃. (B) on reaction with ammonia in presence of anhydrous ZnCI₂ gives (C) of formula C₆H₇N. Identify A, B, C and explain the reactions.
Answer:
1. An aromatic compound (A) of molecular formula C₆H₅Cl is identified as chioro benzene.

2. Chioro benzene on reaction with aqueous NaOH produces phenol as (B).

3. Phenol gives violet colour with neutral FeCI₃. Phenol on treated with NH₃ in the presence of anhydrous ZnCl₂ gives Aniline as (C).

Question 18.
An organic compound (A) of molecular formula C₆H₆O gives white precipitate with bromine water. (A) on reaction with NaOH gives (B). (B) reacts with methyl iodide in presence of dry ether gives (C) of molecular formula C₇H₈O which will not liberate H₂ gas with metallic Na. (C) on reaction with acetvl chloride gives (D) and (E) of formula which are position isomers. Identify A, B, C, D & E and explain the reaction.
Answer:
1. An organic compound gives white precipitate with bromine water means it must be a phenol. From the molecular formula it is identified as C₆H₅OH.

2. Phenol on reaction with NaOH gives (B) as sodium phenoxide C₆H₅ONa.

3. Sodium phenoxide on reaction with methyl iodide in the pressure of dry ether undergo Williamsons synthesis and gives Anisole as (C).

4. Anisole on reaction with acetyl chloride undergoes Fnedel Craft’s acetylation and yield O – methoxy acetophenone and p-methoxy acetophenone as (D) and (E).

Question 19.
An organic compound (A) of molecular formula C₆H₅CI on reaction with aqueous NaOH gives (B) of formula C₆H₆O. (B) on reaction with NaOH gives (C) of formula C₆H₅ONa. (C) on treatment with CO₂, followed by acid hydrolysis yield (D) of formula C₇H₆O₃ an aromatic hydroxy acid. Identify A, B, C, D and explain the reactions involved.
Answer:

1. (A) is identified from the formula as C₆H₅CI – Chloro benzene.
2. Chloro benzene on treatment with aqueous NaOH yeilds C₆H₅OH – phenol as (B).
3. Phenol on reaction with NaOH produces sodium phenoxide C₆H₅ONa as (C).
4. Sodium phenoxide on reaction with CO₂, followed acid hydrolysis, Kolbe’s reaction takes place to give Salicylic acid as (D).

Question 20.
An organic compound (A) of molecular formula C₆HN₂Cl on boiling with hot water gives (B) of molecular formula C₆H₆O. (B) on reaction with Zinc dust gives (C) a simplest aromatic hydrocarbon. (C) on reaction with methyl chloride in the presence of anhydrous AICI₂ gives (D) of molecular formula C₇H₈. Identify A, B, C, D and explain the reaction.
Answer:
1. (A) is identified from the formula as Benzene diazonium chloride – C₆H₅N₂Cl.

2. Benzene diazonium chloride when boiled with hot water produces phenol as (B).

3. Phenol on reaction with Zinc dust gives Benzene as (C) which is simplest aromatic hydrocarbon.

4. Benzene on treatment with (C) methyl chloride in the presence of anhydrous AlCl₃, Friedel Crafts reaction take place and the product formed is Toluene as (D).

Question 21.
An organic compound (A) of molecular formula C₆H₆O gives violet colour with neutral FeCI₃. (A) reacts benzene diazoniurn chloride in basic medium to give (B) as an azo dye. (A) reacts with acidified K₂Cr₂O₇ gives (C) of formula C₆H₄O₂. (A) on reaction with H₂ in the presence of nickel gives (D) of formula C₆H₁₂O. Identify A, B, C, D and explain the reaction involved.
Answer:
1. (A) of molecular formula C₆H₆O gives violet colour with neutral FeCI₃ means it must be Phenol – C₆H₅OH.

2. Phenol couples with benzene diazonium chloride in the presence of basic medium to produce p-hydroxy azo benzene, a red orange dye as (B).

3. Phenol on reaction with acidified K₂Cr₂O₇ undergoes oxidation reaction to give 1, 4 – benzo quinone as (C).

4. Phenol on reaction with H₂, in the presence of Nickel gives cyclohexanol as (D).

Question 22.
An organic compound (A) of molecular formula C₆H₆ reacts with propylene in the presence of H₃PO₄ at 532 K gives (B) of formula C₉H₁₂ . (B)on air oxidation gives C₉H₁₂O₂ as (C). (C) on acidification with H₂SO₄ gives (D) of formula C₆H₆O and (E) of formula C₃H₆O. Identify A, B, C, D and E and explain the reactions.
Answer:
1. (A) is identified as benzene from the molecular formula.

2. Benzene reacts with propylene in the presence of H₃PO₄ gives cumene as (B).

3. Cumene on air oxidation produces cumene hydroperoxide as (C).

4. Cumene hydroperoxide on treatement with H₂SO₄ yield phenol as (D) and acetone as (E).

Question 23.
An organic compound (A) of molecular formula C₂H₆O reacts P/I₂ gives (B) which on further reaction with silver nitrite gives (C) of formula C₂H₅NO₂. (C) on treatment with nitrous acid yield (D) of formula C₂H₄N₂O₃. (D) on reaction with KOH give red color product (E). Identify A, B, C, D and E. From the final product (E) red colour product, it is identified these reactions are the reactions of primary alcohols in Victor Meyer’s test.
Answer:

Question 24.
An organic compound (A) of molecular formula C₃HO on reaction P/I₂ gives C₃H₇I as (B). (B) on reaction with AgNO₂ produces (C) with formula C₃H₇NO₂. (C) on reaction with nitrous acid gives (D) of molecular formula C₃H₆N₂O₃. (D) on reaction with KOH produces blue colour. Identify A, B. C, D and explain the reaction.
Answer:
From the final colour blue, this reaction are considered as reactions of secondary alcohol in Victory Meyer’s. (A) is identified as  2 – propanol.

Question 25.
An organic compound (A) of molecular formula C₄H₁₀O gives no colouration in Victor Meyer’s test. (A) on reaction with P / I₂ gives (B) of formula C₄H₉I. (B) on treatment with nitrous acid gives (C) of formula C₃H₉NO₂. (C) does not react with KOH. Identify A, B, C and explain.
Answer:
C₄H₁₀O gives no colouration in Victor Meyer’s test means it must be tertiary alcohol. So (A) is tertiary butyl alcohol. The reactions involved are,

Common Errors

1. Writing IUPAC names may be difficult and students may get confused.
2. Primary, Secondary and Tertiary alcohols functional groups may get confused. Phenol, aromatic alcohols are differenet.
3. Benzene ring should be drawn properly.
4. Skeleton carbon chain may be a problem to students.

Rectifications

1. Parent hydrocarbon – longest carbon chain. Lowest number of the carbon having functional group. Arrangement of substitutents in alphabetical order. Alcohol – Name should end in the word ol.

2. Primary alcohol – CHI₂OH, Secondary alcohol > CHOH, Tertiary alcohol > COH – OH gp/ directly attached to benzene ring is
Phenol
It is not aromatic alcohol
– OH gp/ is attached to the side chain of the benzene ring is an aromatic alcohol.

Benzyl alcohol

3. Altemat double bond along with regular hexagon is ben zeane.
Benzene (C₆H₆) If you draw the above structure without double bonds, it is cyclo hexane.
Cyclohexane (C₆H₁₂)

4.
CH₃ – CH₂ – CH₂ – CH₂ – CH₂ – CH₂ – CH₃
n-heptane

CH₃ – CH₂ – CH₂ – CH = CH₂
Pent – 1 – ene

We hope the Class 12th Samacheer Kalvi Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Book Solutions Answers Guide Solutions provided here help the students to get the best knowledge. Also, students can use our Samacheer Kalvi Class 12th Chemistry Solutions Chapter 11 Hydroxy Compounds and Ethers Questions and Answers for better practice. You can contact us at any moment by giving comments in the comment section. Keep checking updates by bookmarking our website.