Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. • You do not have to consider stereochemistry.
Include all valence lone pairs in your answer.
. In cases where there is more than one answer, just draw one.

Following are the answer to this question:

Explanation:

In the given example of aromatic electrophilic substitution and transforms toluene into p-isopropyl toluene. The group CH3 is also an initiating group o, p-directing (by + Inductive effect). Throughout this scenario, only para-substitution occurs also because O- replaced steric and unpredictable transitional cation procedures.

Please find the attachment of diagram:

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