Question:

Identify A and B in the following reactions:
nitrobenzene

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In reduction reactions, nitro groups are converted to amine groups, while halogenation typically occurs at the para position in the presence of \(\text{NaOH}\).
Updated On: Jul 11, 2025
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Solution and Explanation

In the given reactions, we need to identify the compounds A and B. The first reaction involves the reduction of a nitro group (\(-\text{NO}_2\)) to an amine group (\(-\text{NH}_2\)) using hydrogen and palladium (\(\text{H}_2/\text{Pd}\)) in ethanol. This suggests A is \textit{nitrobenzene}. The second reaction involves the bromination of A with bromine in the presence of sodium hydroxide (\(\text{NaOH}\)), leading to the formation of B. B is likely to be \(\text{4-bromobenzenamine}\), as the bromine typically substitutes in the para position in the presence of \(\text{NaOH}\). Thus, A = \textit{Nitrobenzene} (\(\text{C}_6\text{H}_5\text{NO}_2\)) B = \(\text{4-Bromobenzenamine}\) (\(\text{C}_6\text{H}_4\text{BrNH}_2\))
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