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
(d) Friedel–Crafts acylation of anisole with CH3CCI
(e) Nitration of isopropyl benzene
(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 CHH CH Br CH H CH Br CH ...View the full answer
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