In a set of reactions, acetic acid yields a product D:
\[
\text{CH}_3\text{COOH} \xrightarrow{\text{SOCl}_2} \text{Benzene} \xrightarrow{\text{AlCl}_3} (B)
\]
\[
\text{HCN} \xrightarrow{\text{(C)}} \text{HOH} \xrightarrow{\text{H}_2\text{O}} (D)
\]
The structure of \( D \) would be:
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Friedel-Crafts acylation is used to add an acyl group (RCO-) to an aromatic ring.
Step 1: Reaction of acetic acid with thionyl chloride.
Acetic acid reacts with thionyl chloride (SOCl\(_2\)) to form acetyl chloride.
Step 2: Friedel-Crafts acylation.
Acetyl chloride reacts with benzene in the presence of AlCl\(_3\) to form acetophenone.
Step 3: Hydrolysis.
The next reaction involves hydrolysis of the nitrile group to form a carboxylic acid, yielding the final product as \( \text{C}_6\text{H}_5\text{COOH} \) (benzoic acid).