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.

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.

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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.​

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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.