Its found experimentally that a substituted cyclohexanol with an axial -OH group reacts with aqueous CrO 3

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It’s found experimentally that a substituted cyclohexanol with an axial -OH group reacts with aqueous CrO3 more rapidly than its isomer with an equatorial -OH group. Draw both cis- and trans-4-tert-butylcyclohexanol, and predict which oxidizes faster.

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