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
Which of the following reagent can be used to convert nitrobenzene to aniline?
\[\ce{CH3CH2Br ->[aq NaOH][\Delta] A ->[KMnO4/H^+][\Delta] B ->[NH3][\Delta] C ->[Br2/NaOH] D}\] ‘D’ is:
Which one of the following nitro compounds does not react with nitrous acid?

‘A’ is:
Secondary nitro alkanes react with nitrous acid to form ____________.
There are two isomers with the formula CH3NO2. How will you distinguish between them?
What happens when 2-Nitropropane boiled with HCl?
How will you convert nitrobenzene into 1, 3, 5-trinitrobenzene?
Identify A, B and C.

Identify A to E in the following sequence of reactions.

