3. Which C7H₁40 isomers give rise to the spectra shown below? (Hint: the IR spectra of both molecules would contain a strong peak at ~1710 cm-¹.) a. C. 8 7 6 6 5 4 8 (ppm) 5 2 4 8 (ppm) Note: From left to right, the peak multiplicities are septet and doublet. 3 All singlets 2 1 1 0
3. Which C7H₁40 isomers give rise to the spectra shown below? (Hint: the IR spectra of both molecules would contain a strong peak at ~1710 cm-¹.) a. C. 8 7 6 6 5 4 8 (ppm) 5 2 4 8 (ppm) Note: From left to right, the peak multiplicities are septet and doublet. 3 All singlets 2 1 1 0
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
Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions
Section: Chapter Questions
Problem 20.25P
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Question
![3. Which C7H₁40 isomers give rise to the spectra shown below? (Hint: the IR spectra of both
molecules would contain a strong peak at ~1710 cm-¹.)
a.
C.
8
7
8
7
6
5
5
4
8 (ppm)
4
8 (ppm)
Note: From left to right, the peak multiplicities are septet and doublet.
3
3
2
All singlets
2
1
0
0](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fef179162-973e-41f0-bb3a-1bfb38a065ce%2Fbdd2e84f-0abc-4121-b17c-292d559ddf9c%2Fjh0kdr_processed.png&w=3840&q=75)
Transcribed Image Text:3. Which C7H₁40 isomers give rise to the spectra shown below? (Hint: the IR spectra of both
molecules would contain a strong peak at ~1710 cm-¹.)
a.
C.
8
7
8
7
6
5
5
4
8 (ppm)
4
8 (ppm)
Note: From left to right, the peak multiplicities are septet and doublet.
3
3
2
All singlets
2
1
0
0
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