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(C) The electrolytic reduction of nitrobenzene in the presence of concentrated $H_2SO_4$ proceeds through the formation of phenylhydroxylamine. This i

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$p$-aminophenol

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(C) The electrolytic reduction of nitrobenzene in the presence of concentrated $H_2SO_4$ proceeds through the formation of phenylhydroxylamine. This intermediate undergoes a Bamberger rearrangement in the acidic medium to form $p$-aminophenol as the final product. The reaction sequence is: $C_6H_5NO_2$ $\xrightarrow{[H], H_2SO_4} C_6H_5NHOH$ $\xrightarrow{H_2SO_4} p-H_2NC_6H_4OH$.

The product obtained by the electrolytic reduction of nitrobenzene in the presence of $H_2SO_4$ is:

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