Question 3: 2-tertbutylcyclohexanol is quickly oxidized to the corresponding ketone when treated with chromium trioxide, as shown below. OH XOH tBu OH CrO3 A cis isomer (B) trans isomer O... tBu tBu The reaction tends to proceed more quickly when the -OH is placed in the equatorial position. Given this information, which isomer if 2- tBu tertbutylcyclohexanol would you expect undergo oxidation more rapidly? both will react with an equal rate 0

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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
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Question 3: 2-tertbutylcyclohexanol is quickly
oxidized to the corresponding ketone when treated
with chromium trioxide, as shown below.
OH
tBu
OH
CrO3
B trans isomer
Q..
tBu
tBu
The reaction tends to proceed more quickly when
the -OH is placed in the equatorial position. Given
this information, which isomer if 2-
tertbutylcyclohexanol would you expect undergo
oxidation more rapidly?
(A) cis isomer
C both will react with an equal rate
tBu
Transcribed Image Text:Question 3: 2-tertbutylcyclohexanol is quickly oxidized to the corresponding ketone when treated with chromium trioxide, as shown below. OH tBu OH CrO3 B trans isomer Q.. tBu tBu The reaction tends to proceed more quickly when the -OH is placed in the equatorial position. Given this information, which isomer if 2- tertbutylcyclohexanol would you expect undergo oxidation more rapidly? (A) cis isomer C both will react with an equal rate tBu
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