Acid-catalyzed hydrolysis of a 1, 2-epoxycyclohexane produces a trans-diaxial 1, 2diol. What product would you expect to

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Acid-catalyzed hydrolysis of a 1, 2-epoxycyclohexane produces a trans-diaxial 1, 2—diol. What product would you expect to obtain from acidic hydrolysis of cis-3-tert-butyl-1, 2-epoxycyclohexane? (Recall that the bulky tert-butyl group locks the cyclohexane ring into a specific conformation.)

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