Step 1: Understanding Reactivity of Benzyl Halides Benzyl halides are more reactive than aryl halides because the benzylic position stabilizes carbocation intermediates. Step 2: Analyzing the Reaction Mechanism The amine group (\( NH_3 \)) undergoes nucleophilic substitution at the benzylic position. The bromine remains intact since the benzyl chloride reacts first due to higher reactivity. Step 3: Identifying the Correct Product The correct product is the one where amination occurs at the benzylic carbon, leading to o-bromobenzylamine. Thus, the correct answer is (C).
