Nitrobenzene into aniline

Nitrobenzene into N - phenyl hydrazobenzene

Nitrobenzene into hydrazobenzene

Nitrobenzene into azoxybenzene
+3H₂O

Nitrobenzene into m - nitro aniline
  + 6NH₃ + 2H₂O + 3S

Nitrobenzene into o - and p - nitro phenols

iv) Oxidation of acetoneoxime with trifluoroperoxy acetic acid.

It gives 2 - nitro propane.

iii) Oxidation of text – butylamine with KMnO₄:

It gives 2 - methyl - 2- nitro propane is obtained.

ii) Nitrobenzene on electrolytic reduction in strongly acidic medium:

It gives aniline, phenyl hydroxylamine and p - amino phenol

a) Primary and secondary nitroalkanes, having α-H, also show an equilibrium mixture of two tautomers namely nitro - and aci - form

b) Difference:

Nitrobenzene into 1,3,5 - trinitro benzene

Nitrobenzene                                 1,3,5 - trinitro benzene
ii. Nitrobenzene into o - and p - nitro phenols

iii. Nitrobenzene into m - nitro aniline
  + 6NH₃ + 2H₂O + 3S
iv. Nitrobenzene into azoxybenzene
+3H₂O
v. Nitrobenzene into hydrazobenzene

vi. Nitrobenzene into N - phenyl hydrazobenzene

vii. Nitrobenzene into aniline

i) 2 - nitro propane is boiled with HCI:

It gives acetone.
ii) Nitrobenzene on electrolytic reduction in strongly acidic medium:

It gives aniline, phenyl hydroxylamine and p - amino phenol
iii) Oxidation of text – butylamine with KMnO₄:

It gives 2 - methyl - 2- nitro propane is obtained.
iv) Oxidation of acetoneoxime with trifluoroperoxy acetic acid.

It gives 2 - nitro propane.