1. (A) Amide \( R-C=O-NH_2 \):
To reduce an amide \( R-C=O-NH_2 \) to an amine, we use \( LiAlH_4 \) and \( H_2O \) (reagent III). \( LiAlH_4 \) is a strong reducing agent that reduces amides to amines.
2. (B) Nitrobenzene \( C_6H_5NO_2 \):
Nitrobenzene is reduced to aniline using \( H_2/Ni \) (reagent II), which is a catalytic hydrogenation process.
3. (C) Nitrile \( R-C \equiv N \):
Nitriles are reduced to amines using \( Sn \) and \( HCl \) (reagent IV), where the nitrile group is reduced to a primary amine.
4. (D) Aniline \( C_6H_5NH_2 \):
Aniline undergoes reduction by aqueous \( NaOH \) (reagent I), which can be used to dealkylate aromatic amines under certain conditions.
\[ (A) \to (III), \quad (B) \to (II), \quad (C) \to (IV), \quad (D) \to (I) \]
Complete the following equation :
Write the products of the following reactions:
Predict the major product $ P $ in the following sequence of reactions:
(i) HBr, benzoyl peroxide
(ii) KCN
(iii) Na(Hg), $C_{2}H_{5}OH$