In organic chemistry, Friedel Craft reaction holds its own importance for synthesizing alkyl-aryl or acyl-aryl compounds in the presence of Lewis acid. This reaction was first reported in 1887 by Charles Friedel and James Mason Craft for their isolation of amyl benzene under the action of Lewis acid. However, the yield was found to be low due to the formation of other side products in the reaction. The reaction termed Friedel Craft alkylation. This reaction generally involves Lewis acids such as FeBr3, AlCl3, SnCl4, TiCl4, BF3, BeCl2, etc. The mechanism of the reaction shows the formation of carbocation which rearranges itself to direct the reaction in the forward reaction. Due to the formation of carbocations n-alkyl substituted product is difficult to form in this route. Let us understand the mechanism of the reaction step by step. The first point is the interaction of Lewis acid with the alkyl halide. The lone pair of halide interact with the vacant p-orbital of the Lewis acid and