E1 eliminations of alkyl halides are rarely useful for synthetic purposes because they give mixtures of substitution and elimination products. Explain why the sulfuric acid-catalyzed dehydration of cyclohexanol gives a good yield of cyclohexene even
though the reaction goes by an E1 mechanism. (Hint: What are the nucleophiles in the reaction mixture? What products are
formed if these nucleophiles attack the carbocation? What further reactions can these substitution products undergo?)
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