Below are the structures for trans-1-chloro-2-t-butylcyclohexane and cis-1- chloro-2-t-butylcyclohexane. Both molecules can react with a base to form an alkene. cis-1-chloro-2-t-butylcyclohexane reacts 10x faster than trans-1-chloro2-t-butylcyclohexane. Use chair conformations to explain why the cis isomer is more reactive.
Below are the structures for trans-1-chloro-2-t-butylcyclohexane and cis-1- chloro-2-t-butylcyclohexane. Both molecules can react with a base to form an alkene. cis-1-chloro-2-t-butylcyclohexane reacts 10x faster than trans-1-chloro2-t-butylcyclohexane. Use chair conformations to explain why the cis isomer is more reactive.
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Below are the structures for trans-1-chloro-2-t-butylcyclohexane and cis-1-
chloro-2-t-butylcyclohexane. Both molecules can react with a base to form an
alkene . cis-1-chloro-2-t-butylcyclohexane reacts 10x faster than trans-1-chloro2-t-butylcyclohexane. Use chair conformations to explain why the cis isomer is
more reactive.
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