The electrophilic bromination or chlorination of benzene requires Lewis acid along with the halogen.
The bromination or chlorination of benzene is an example of an electrophilic aromatic substitution reaction.
During the reaction, the bromine forms a sigma bond to the benzene ring, yielding an intermediate. Subsequently a a proton is removed from the intermediate to form a substituted benzene ring.
This reaction is achieved with the help of Lewis acid as catalysts.
Thus, the electrophilic bromination or chlorination of benzene requires Lewis acid along with the halogen.
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