[5 points] A compound X (molecular formula C6H12O2) gives a strong peak in its IR spectrum at 1740 cm ¹. The 1H NMR spectrum of X shows only two singlets, including one at 3.5 ppm. The 13C NMR spectrum is given below. Propose a structure for X. 180 160 140 120 100 PPM 80 60 60 40 40 20 20
[5 points] A compound X (molecular formula C6H12O2) gives a strong peak in its IR spectrum at 1740 cm ¹. The 1H NMR spectrum of X shows only two singlets, including one at 3.5 ppm. The 13C NMR spectrum is given below. Propose a structure for X. 180 160 140 120 100 PPM 80 60 60 40 40 20 20
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
Chapter13: Nuclear Magnetic Resonance Spectroscopy
Section: Chapter Questions
Problem 13.17P: Following are 1H-NMR spectra for compounds G, H, and I, each with the molecular formula C5H12O. Each...
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![[5 points] A compound X (molecular formula C6H12O2) gives a strong peak in its IR spectrum at 1740
cm ¹. The 1H NMR spectrum of X shows only two singlets, including one at 3.5 ppm. The 13C NMR
spectrum is given below. Propose a structure for X.
180
160
140
120
100
PPM
80
60
60
40
40
20
20](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F0db91a56-614f-45ad-8d1f-9b79a1c3c3ed%2F404e844b-7253-426b-b51f-05762665ca2e%2Fp28n3_processed.png&w=3840&q=75)
Transcribed Image Text:[5 points] A compound X (molecular formula C6H12O2) gives a strong peak in its IR spectrum at 1740
cm ¹. The 1H NMR spectrum of X shows only two singlets, including one at 3.5 ppm. The 13C NMR
spectrum is given below. Propose a structure for X.
180
160
140
120
100
PPM
80
60
60
40
40
20
20
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