Identify product C in the following conversio | vedclass

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(B) Step $1$: Protection of the $-OH$ group of $m$-hydroxybenzaldehyde with benzyl chloride $(C_6H_5CH_2Cl)$ gives $m$-benzyloxybenzaldehyde $(A)$.Ste

Vedclass · Accepted Answer

$m$-Hydroxybenzoic acid

Vedclass · Answer

(B) Step $1$: Protection of the $-OH$ group of $m$-hydroxybenzaldehyde with benzyl chloride $(C_6H_5CH_2Cl)$ gives $m$-benzyloxybenzaldehyde $(A)$.Step $2$: Oxidation of the aldehyde group in $A$ using an oxidizing agent $[O]$ yields $m$-benzyloxybenzoic acid $(B)$.Step $3$: Deprotection of the benzyl group (usually via catalytic hydrogenation or acid-catalyzed cleavage) removes the protecting group to yield $m$-hydroxybenzoic acid $(C)$.

Identify product $C$ in the following conversion sequence: $m$-Hydroxybenzaldehyde $\xrightarrow[\text{Protection of } -OH \text{ group}]{C_6H_5CH_2Cl} A$ $\xrightarrow{[O]} B$ $\xrightarrow{\text{deprotection}} C$.

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