An electrophilic aromatic substitution occurs when benzene is attacked by an electrophile and is substituted by hydrogen, since halogens are not sufficiently electrophile to break the aromatic benzene so a catalyst is needed to break the benzene ring.
Chlorobenzene reacts with chlorine gas and forms dichlorobenzene at the ortho and para positions by initiating the chromium ion.
There is a deactivation of chlorine ion but the ortho and para are directing.
The general equation of halogenation of benzene is shown below:
The importance of in halogenation of benzene:
Arenes react with the halogens in the presence of (Lewis acid) to form haloarenes.
When acts as Lewis acid in the reaction then there is a replacement of the chlorine atom in the place of a hydrogen atom from the benzene ring.
Chlorine polarizes in the substitution reaction by introducing a positive charge on the chlorine tom due to the as Lewis base in the reaction.