5. A Compound (C7H₁40) has a strong infrared absorption at 1715 cm¹. The ¹HNMR spectrum has two signals at 8 1.10 (doublet) and 8 2.77 (septet), ratio 6:1. The 13CNMR spectrum shows three lines at 8 218, 39, and 18. Which of the following structure best fits with this spectroscopic data? H 2
5. A Compound (C7H₁40) has a strong infrared absorption at 1715 cm¹. The ¹HNMR spectrum has two signals at 8 1.10 (doublet) and 8 2.77 (septet), ratio 6:1. The 13CNMR spectrum shows three lines at 8 218, 39, and 18. Which of the following structure best fits with this spectroscopic data? H 2
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
Chapter14: Mass Spectrometry
Section: Chapter Questions
Problem 14.27P: Following is the mass spectrum of an unknown compound. The two highest peaks are at m/z 120 and 122....
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![5. A Compound (C7H140) has a strong infrared absorption at 1715 cm³¹. The ¹HNMR
spectrum has two signals at 8 1.10 (doublet) and 8 2.77 (septet), ratio 6:1.
The 13CNMR spectrum shows three lines at 8 218, 39, and 18.
Which of the following structure best fits with this spectroscopic data?
X
H
?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fd0f9e2f8-43df-4240-86bc-25bf307c27d3%2F4bacfd85-576a-48c5-ad3d-d336fd3dc004%2Fbn4svmj_processed.jpeg&w=3840&q=75)
Transcribed Image Text:5. A Compound (C7H140) has a strong infrared absorption at 1715 cm³¹. The ¹HNMR
spectrum has two signals at 8 1.10 (doublet) and 8 2.77 (septet), ratio 6:1.
The 13CNMR spectrum shows three lines at 8 218, 39, and 18.
Which of the following structure best fits with this spectroscopic data?
X
H
?
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