The reaction of chloro benzene with acetyl chloride in the presence of anhydrous AlCl\(_3\) is an example of electrophilic substitution. In this reaction, AlCl\(_3\) acts as a catalyst and facilitates the substitution of a hydrogen atom on the benzene ring with an acetyl group (-COCH\(_3\)), resulting in the formation of 4-chloroacetophenone.
- Nucleophilic substitution involves the replacement of a leaving group by a nucleophile, which is not the mechanism here.
- Nucleophilic addition involves the addition of a nucleophile to a carbonyl group, which is also not the mechanism here.
Thus, the correct answer is electrophilic substitution, where the acetyl group is electrophilic and substitutes a hydrogen atom on the aromatic ring.