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Question

(C) $2,2,2-$trichloroacetophenone reacts with aqueous $KOH$ via a haloform-like cleavage reaction. The hydroxide ion attacks the carbonyl carbon,follo

Vedclass · Accepted Answer

Benzoic acid

Vedclass · Answer

(C) $2,2,2-$trichloroacetophenone reacts with aqueous $KOH$ via a haloform-like cleavage reaction. The hydroxide ion attacks the carbonyl carbon,followed by the departure of the stable $CHCl_3$ (chloroform) leaving group to form the potassium salt of benzoic acid. Subsequent acidification with $H_3O^+$ yields benzoic acid as the final product $P$.Thus,option $(c)$ is the correct answer.

One of the products of the following reaction is $P$. Structure of $P$ is

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