The products formed in the following reaction sequence are :

- (A)(see structure)

- (B)(see structure)

- (C)(see structure),
✓ Correct
- (D)(see structure),

Answer: (C)
Solution
Starting from nitrobenzene:
brominates the ring ortho/para to the nitro group, giving a bromonitrobenzene.
reduces the nitro group to an amine, giving a bromoaniline.
at diazotises the amine to the aryldiazonium chloride.
then reduces the diazonium salt: ethanol replaces with while itself being oxidised to acetaldehyde, releasing nitrogen:
The products are bromobenzene and acetaldehyde.
brominates the ring ortho/para to the nitro group, giving a bromonitrobenzene.
reduces the nitro group to an amine, giving a bromoaniline.
at diazotises the amine to the aryldiazonium chloride.
then reduces the diazonium salt: ethanol replaces with while itself being oxidised to acetaldehyde, releasing nitrogen:
The products are bromobenzene and acetaldehyde.

JEE Main · 2025 · 22 Jan 2025 · Shift 1 · Single correct option