Me Me Ме Me Ме H20 Br Br HO. + Но H Et Et RDS Et H Et Et transition state carbocation intermediate 우

Pushing Electrons
4th Edition
ISBN:9781133951889
Author:Weeks, Daniel P.
Publisher:Weeks, Daniel P.
Chapter1: Lewis Structures
Section: Chapter Questions
Problem 63EQ
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c. Snl reactions dominate under polar protic solvents. Increasing the polarity of the solvent will increase
the rate of the reaction because the polar solvent will stabilize the dispersed charges on the transition
state more than it will stabilize the neutral reactant. Label areas of ô* and & on the molecules of the
transition state of the SN1 reaction below:
Me
Me
Ме
Me
Me
H20
Br
-Br
OH
+
НО
\'H
Et
Et
RDS
Et
H Et
Et
transition state
not isolable
carbocation intermediate
not isolable
Transcribed Image Text:c. Snl reactions dominate under polar protic solvents. Increasing the polarity of the solvent will increase the rate of the reaction because the polar solvent will stabilize the dispersed charges on the transition state more than it will stabilize the neutral reactant. Label areas of ô* and & on the molecules of the transition state of the SN1 reaction below: Me Me Ме Me Me H20 Br -Br OH + НО \'H Et Et RDS Et H Et Et transition state not isolable carbocation intermediate not isolable
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