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Chemistry, 30.07.2021 02:10, bobelliot67789
During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene ring, that direct ortho/para further stabilize this intermediate by participating in the resonance delocalization of the positive charge. Assume that the following group is present on a benzene ring at position 1 and that you are brominating the ring at positon 4. Draw the structure of the resonance contributor that shows this group actively participating in the charge delocalization. OCH3
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During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Gr...
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