Step 1: Benzyl Halide Reactivity Analysis Benzyl halides exhibit greater reactivity compared to aryl halides due to the stabilization of carbocation intermediates at the benzylic position. Step 2: Reaction Mechanism Examination The amine group (\( NH_3 \)) participates in a nucleophilic substitution reaction at the benzylic carbon. The bromine atom remains unaffected as the benzyl chloride undergoes reaction initially, owing to its superior reactivity. Step 3: Determination of the Final Product The resultant product is formed via amination at the benzylic carbon, yielding o-bromobenzylamine. Consequently, the accurate option is (C).
