Answer:
See explanation
Step-by-step explanation:
The chlorination of benzene occurs in the presence of a Lewis acid. A Lewis acid is a compound that can accept a lone pair of electrons.
The first step in the chlorination of benzene is the formation of the ion Cl^+ which attacks the benzene ring.
This ion is formed when the Cl2 molecule undergoes heterolytic fission assisted by FeCl3 to yield FeCl4^- and Cl^+.
The Cl^+ electrophile now attacks the benzene ring to yield chlorobenzene.