Answer:
CH3Cl reacts with AlCl3 to give (CH3)+ and (AlCl4)-. AlCl3 acts as a Lewis acid and CH3Cl acts as a Lewis base. The
The (CH3)+ generated will then act as an electrophile to substitute a H on benzene. The product is toluene together with HCl as a side product.
This is an electrophilic substitution type reaction.