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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To answer this question lets first draw both cis and trans4tertbutylcyclohexanol The OH group can be ...View the full answer
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