Electrolytic reduction of nitrobenzene in weakly acidic medium givesN-PhenylhydroxylamineNitrosobenzeneAnilinep-Hydroxyaniline
Question
Electrolytic reduction of nitrobenzene in weakly acidic medium givesN-PhenylhydroxylamineNitrosobenzeneAnilinep-Hydroxyaniline
Solution
The electrolytic reduction of nitrobenzene in a weakly acidic medium primarily gives Aniline. Here's a step-by-step explanation:
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Nitrobenzene (C6H5NO2) is subjected to electrolytic reduction, which means it is reduced by gaining electrons. This process is carried out in a weakly acidic medium.
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During the reduction, the nitro group (NO2) in nitrobenzene is reduced to an amino group (NH2), resulting in the formation of aniline (C6H5NH2).
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The reaction can be represented as follows: C6H5NO2 + 6[H] → C6H5NH2 + 2H2O. Here, [H] represents the hydrogen ions provided by the acidic medium and the electrons gained during reduction.
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Therefore, the primary product of the electrolytic reduction of nitrobenzene in a weakly acidic medium is aniline.
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