Question: Draw resonance structures of the intermediate carbocations in the bromination of naphthalene, and account for the fact that naphthalene undergoes electrophilic substitution at C1 rather
Draw resonance structures of the intermediate carbocations in the bromination of naphthalene, and account for the fact that naphthalene undergoes electrophilic substitution at C1 rather than C2.

Br Br2 Br2
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Resonance forms for the intermediate from attack at C1 Br H 8888 080828 H B... View full answer
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