MCQEasyJEE 2023Carboxylic Acids

JEE Chemistry 2023 Question with Solution

Given below are two statements: One is labelled as Assertion A and the other is labelled as Reason R.

Assertion A: \ceCH3COOH\ce{CH3COOH} can be easily reduced using Zn-Hg/HCl to \ceCH3CH2OH\ce{CH3CH2OH}.

Reason R: Zn-Hg/HCl is used to reduce carbonyl group to \ceCH2\ce{-CH2-} group.

In the light of the above statements, choose the correct answer from the options given below:

  • A

    A is false but R is true

  • B

    A is true but R is false

  • C

    Both A and R are true but R is not the correct explanation of A

  • D

    Both A and R are true and R is the correct explanation of A

Answer

Correct answer:A

Step-by-step solution

Standard Method

Given: Assertion A says \ceCH3COOH\ce{CH3COOH} can be easily reduced using Zn-Hg/HCl to \ceCH3CH2OH\ce{CH3CH2OH}. Reason R says Zn-Hg/HCl reduces a carbonyl group to a \ceCH2\ce{-CH2-} group.

Find: Which option correctly evaluates Assertion AA and Reason RR.

Zn-Hg/HCl is the Clemmensen reduction reagent. It is used to reduce the carbonyl group of aldehydes and ketones to a methylene group.

\ceRCOR>[ZnHg/HCl]RCH2R\ce{R-CO-R' ->[Zn-Hg/HCl] R-CH2-R'}
Reaction scheme showing a carboxylic acid containing substrate treated with Zn-Hg and HCl, leading to substitution by chlorine instead of desired alcohol formation.

Therefore, Reason RR is true.

Assertion AA is false because a carboxylic acid such as \ceCH3COOH\ce{CH3COOH} is not easily reduced by Zn-Hg/HCl to \ceCH3CH2OH\ce{CH3CH2OH}. The strongly acidic medium makes Clemmensen reduction unsuitable for this conversion. The acid sensitive alcohol group reacts with HCl, hence this method is not suitable for the above conversion.

Therefore, the correct option is A.

Why Assertion Fails

Given: The reagent is Zn-Hg/HCl.

Find: Whether it can convert \ceCH3COOH\ce{CH3COOH} into \ceCH3CH2OH\ce{CH3CH2OH}.

Clemmensen reduction works for aldehydes and ketones, where the carbonyl carbon is reduced all the way to a methylene carbon. It does not serve as a general reducing agent for converting carboxylic acids into primary alcohols.

Also, the medium contains concentrated HCl, so acid-sensitive functionalities do not survive appropriately under these conditions. Hence the proposed conversion in Assertion AA is not valid, even though the general statement in Reason RR about reduction of carbonyl groups to \ceCH2\ce{-CH2-} is correct.

Thus, Assertion A is false but Reason R is true.

Common mistakes

  • Treating all carbonyl-containing compounds as equally reducible by Zn-Hg/HCl is incorrect. Clemmensen reduction is mainly for aldehydes and ketones, not for converting carboxylic acids into alcohols.

  • Assuming that because Reason RR is true, Assertion AA must also be true is incorrect. The reagent property stated in RR does not apply to the specific carboxylic acid conversion in AA.

  • Ignoring the strongly acidic HCl medium is a mistake. Reaction conditions matter, and acid-sensitive situations can make Clemmensen reduction unsuitable.

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