There are two stereoisomers of 1-tert-butyl-4-chlorocyclohexane. One of these isomers reacts with sodium ethoxide in an E2
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There are two stereoisomers of 1-tert-butyl-4-chlorocyclohexane. One of these isomers reacts with sodium ethoxide in an E2 reaction that is 500 times faster than the reaction of the other isomer. Identify the isomer that reacts faster, and explain the difference in rate for these two isomers.
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Because of the bulky tertbutyl group the trans isomer is essentially locked in a chai...View the full answer
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