Reaction: Nitration of aniline using concentrated nitric acid and sulfuric acid.
\[ {C6H5NH2 + HNO3} \xrightarrow{{H2SO4}} {p-C6H4(NO2)NH2} \]
Explanation: Aniline reacts with nitrating mixture to give para-nitroaniline as the major product due to the activating nature of the –NH\(_2\) group.
Reaction: Chlorination of aniline in the presence of ferric chloride as a Lewis acid catalyst.
\[ {C6H5NH2 + Cl2} \xrightarrow{{FeCl3}} {C6H4ClNH2} \]
Explanation: Chlorine reacts with aniline to give substituted products. The reaction is usually controlled to obtain mono-chlorinated derivative such as chlorobenzene.
Reaction: Oxidation of aniline with potassium dichromate in acidic medium.
\[ {C6H5NH2 + K2Cr2O7 + H2SO4} \rightarrow {C6H5OH} \]
Explanation: The –NH\(_2\) group of aniline is oxidized to a hydroxyl group, yielding phenol.
