Advertisements
Advertisements
Question
What happens when Nitrobenzene undergoes electrolytic reduction in a strongly acidic medium?
Advertisements
Solution
Electrolytic reduction of nitrobenzene in weakly acidic medium gives aniline but in strongly acidic medium, it gives p-amino phenol obviously through the acid catalysed rearrangement of the initially formed phenyl hydroxylamine.

APPEARS IN
RELATED QUESTIONS
The method by which aniline cannot be prepared is ____________.
C5H13N reacts with HNO2 to give an optically active compound – The compound is ____________.
Among the following, the reaction that proceeds through an electrophilic substitution is:
There are two isomers with the formula CH3NO2. How will you distinguish between them?
What happens when 2-Nitropropane boiled with HCl?
Identify compounds A, B and C in the following sequence of reaction.
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[HNO2][273 K] B ->[C6H5OH] C}\]
Identify A to E in the following sequence of reactions.

Account for the following
Aniline does not undergo Friedel–Crafts reaction
Account for the following.
Aniline does not undergo Friedel–Crafts reaction
Account for the following:
Aniline does not undergo Friedel – Crafts reaction.
