The reaction between the alkyl halide and acyl halide in the presence of Lewis acid is called the Friedel-craft reaction.
The difference between the alkyl group and acyl group reaction is that during alkylation the benzene attack first on the carbon that attracts the electron-rich elements and during acylation, the pi-bond between C-O break first.
The reaction between Anisole and Ethanoyl chloride in the presence of anhydrous Aluminum chloride to form 2-Methoxy-acetophenone at ortho and para position with minor and major products.
The general reaction of the Friedel-craft reaction is shown below:
The importance of Aluminum chloride in the Friedel-craft reaction is given below:
It acts as a Lewis acid that undergoes an electrophile substitution reaction.
Aluminum chloride is a covalent compound in which three Aluminum electrons are shared with the three Chlorine atoms through a covalent bond. It acts as an electrophile due to electron deficiency.
Lewis acid removes the halide from the alkyl halide and acyl halide and forms carbocation.