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

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter8: Addition Via Carbocation
Section: Chapter Questions
Problem 8E
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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
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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