1. Which 2 isomers would react fastest in an SN2 reaction? 2. Which 4 isomers could participate in both SN1 and E2? 3. Which 4 isomers could create terminal alkenes in bimolecular elimination? 4. Which 2 isomers would not work in E1/E2 but could react in SN1/SN2? 5. Which 4 isomers would not participate in substitution or elimination? 6. Which isomer could participate in SN1 but not SN2? 7. Which 3 isomers contain secondary leaving groups? 8. Which 3 isomers could create resonance stabilized carbocations?
1. Which 2 isomers would react fastest in an SN2 reaction? 2. Which 4 isomers could participate in both SN1 and E2? 3. Which 4 isomers could create terminal alkenes in bimolecular elimination? 4. Which 2 isomers would not work in E1/E2 but could react in SN1/SN2? 5. Which 4 isomers would not participate in substitution or elimination? 6. Which isomer could participate in SN1 but not SN2? 7. Which 3 isomers contain secondary leaving groups? 8. Which 3 isomers could create resonance stabilized carbocations?
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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1. + 2.

Transcribed Image Text:Twelve constitutional isomers exist with the molecular formula C4H¬Br. Answer the following questions
concerning their reactivity in substitution/elimination reactions. Assume no rearrangements occur.
Br
Br
Me
Me
Br
Me
Br
Me
Br
Me
Me
A
В
C
D
E
F
Me
Me
Me
Br
Br
Br
Br
Br
Br
Me
Me
G
J
K
1.
Which 2 isomers would react fastest in an SN2 reaction?
2. Which 4 isomers could participate in both SN1 and E2?
3. Which 4 isomers could create terminal alkenes in bimolecular elimination?
4. Which 2 isomers would not work in E1/E2 but could react in SN1/SN2?
5. Which 4 isomers would not participate in substitution or elimination?
6.
Which isomer could participate in SN1 but not SN2?
7. Which 3 isomers contain secondary leaving groups?
8.
Which 3 isomers could create resonance stabilized carbocations?
1
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