Write a structural formula for the most stable cyclohexadienyl cation intermediate formed in each of the following
Question:
(a) Bromination of p-xylene
(b) Chlorination of m-xylene
(c) Nitration of acetophenone
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(e) Nitration of isopropylbenzene
(f ) Bromination of nitrobenzene
(g) Sulfonation of furan
(h) Bromination of pyridine
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a There are three principal resonance forms of the cyclohexadienyl cation intermediate formed by attack of bromine on pxylene Any one of these resonan...View the full answer
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