9. Identify the major product of each reaction and indicate whether the reaction is likely to proceed by a bimolecular (S2) or a unimolecular (SN1) mechanism. Why is each reaction likely to proceed via the mechanism you have chosen? (Hint: The leaving groups -OSO₂CF3 and -OMs are also sulfonates (like tosylate, -OTS), so they are also good leaving groups.) a) b) oso,CF, Br OMS Nal acetone CH,OH 80% H₂O, 20 % ethanol

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter14: Elimination
Section: Chapter Questions
Problem 36E
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9. Identify the major product of each reaction and indicate whether the reaction is likely
to proceed by a bimolecular (SN2) or a unimolecular (SN1) mechanism. Why is each
reaction likely to proceed via the mechanism you have chosen? (Hint: The leaving
groups -OSO2CF3 and -OMs are also sulfonates (like tosylate, -OTS), so they are
also good leaving groups.)
a)
b)
d)
Oso₂CF,
OMs
Br
Nal
acetone
NaCN
DMF
CH₂OH
80% H₂O, 20% ethanol
-6-
Transcribed Image Text:9. Identify the major product of each reaction and indicate whether the reaction is likely to proceed by a bimolecular (SN2) or a unimolecular (SN1) mechanism. Why is each reaction likely to proceed via the mechanism you have chosen? (Hint: The leaving groups -OSO2CF3 and -OMs are also sulfonates (like tosylate, -OTS), so they are also good leaving groups.) a) b) d) Oso₂CF, OMs Br Nal acetone NaCN DMF CH₂OH 80% H₂O, 20% ethanol -6-
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