Advertisements
Advertisements
प्रश्न
What happens when Nitrobenzene undergoes electrolytic reduction in a strongly acidic medium?
Advertisements
उत्तर
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
संबंधित प्रश्न
Nitrobenzene on reaction with at 80-100°C forms which one of the following products?
C5H13N reacts with HNO2 to give an optically active compound – The compound is ____________.
Secondary nitro alkanes react with nitrous acid to form ____________.
When
is reduced with Sn/HCl the pair of compounds formed are ____________.
Write down the possible isomers of the C4H9NO2 give their IUPAC names.
What happens when oxidation of tert-butylamine with KMnO4?
How will you convert nitrobenzene into hydrozobenzene?
How will you convert nitrobenzene into aniline?
Identify compounds A, B and C in the following sequence of reaction.
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[HNO2][273 K] B ->[C6H5OH] C}\]
Account for the following.
Aniline does not undergo Friedel–Crafts reaction.
