Write a structural formula for the most stable cyclohexadienyl cation intermediate formed in each of the following reactions. Is this intermediate more or less stable than the one formed from benzene?
(a) Bromination of p-xylene
(b) Chlorination of m-xylene
(c) Nitration of acetophenone
(d) Friedel-Crafts acylation of anisole with acetyl chloride
(e) Nitration of isopropylbenzene
(f) Bromination of nitrobenzene
(g) Sulfonation of furan
(h) Bromination of pyridine
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