The cis isomer of 4-tert-butyl-1-bromocyclohexane undergoes E2 elimination about 1,000 times faster than the trans isomer. Explain why the cis isomer reacts faster. (Hint: It is not because of steric hindrance.) Br + NaOH Fast (H,C)C (H,C),C Br + NaOH Slow (H,C),C (H,C),C

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8.32 The cis isomer of 4-tert-butyl-1-bromocyclohexane undergoes E2 elimination about 1,000 times faster than the trans
isomer. Explain why the cis isomer reacts faster. (Hint: It is not because of steric hindrance.)
Br
NaOH
Fast
(H;C),C
(H3C),C
Br
NaOH
Slow
(H,C),C
(H,C),C
Transcribed Image Text:8.32 The cis isomer of 4-tert-butyl-1-bromocyclohexane undergoes E2 elimination about 1,000 times faster than the trans isomer. Explain why the cis isomer reacts faster. (Hint: It is not because of steric hindrance.) Br NaOH Fast (H;C),C (H3C),C Br NaOH Slow (H,C),C (H,C),C
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