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Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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
Transcribed Image Text:Why does a carbocation (right) form, as opposed to tert-pentyl chloride in one concerted step?
Тонг
Select one or more:
slow
a.
Chloride is a hindered nucleophile
b.
The positive charge on the carbocation is stabilized through resonance
C.
The carbocation intermediate is very stable
d.
The methyl and ethyl groups sterically block an SN₂ backside attack
H₂O
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