Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the α position. Predict the major products of the reactions of naphthalene with the following reagent.
(a) HNO3, H2SO4
(b) Br2, FeBr3
(c) CH3CH2COCl,
(d) isobutylene and HF
(e) cyclohexanol and BF3
(f) fuming sulfuric acid
Electrophilic aromatic substitution usually occurs at the 1-position of naphthalene, also called the α position. Predict the major products of the reactions of naphthalene with the following reagent.
(a) HNO3, H2SO4
(b) Br2, FeBr3
(c) CH3CH2COCl,
(d) isobutylene and HF
(e) cyclohexanol and BF3
(f) fuming sulfuric acid
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