Br Br „Me Me Br Me Br Me Br Me Ме A В D F Me Br Me Ме Br Br Br Br -Br Me Me G J 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
Br Br „Me Me Br Me Br Me Br Me Ме A В D F Me Br Me Ме Br Br Br Br -Br Me Me G J 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
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter21: Benzene And The Concept Of Aromaticity
Section: Chapter Questions
Problem 21.44P
Related questions
Question
7.+ 8.
![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](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd7323f76-5a9c-46b6-9930-86cefe6607d1%2Fc93fd886-f19d-4b29-be11-e0f316dd1408%2Fwtqfcka_processed.jpeg&w=3840&q=75)
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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