- Reaction I: This is an alkylation reaction of an alkyl halide (R-X) with ammonia (NH₃). It yields a primary amine (R-NH₂) by substitution.
- Reaction II: This reaction involves the reduction of a nitrile (R-C≡N) to a primary amine (R-CH₂NH₂) under catalytic hydrogenation conditions (H₂/Ni).
- Reaction III: In this case, a nitrile (R-C≡N) is hydrolyzed with acidic water (H₂O + H⁺), which leads to the formation of a carboxylic acid (R-COOH), not an amine.
- Reaction IV: Here, a primary amide (R-C-NH₂) undergoes reduction with LiAlH₄ to form an amine (R-CH₂NH₂).
Thus, reaction III does not yield an amine, as it produces a carboxylic acid instead. Therefore, the correct answer is Option 2 (Only III).