An unknown compound has a molecular formula of C,H,O. Its IR spectrum shows prominent absorptions at 2980, 2960, and 1718 cm. It exhibits the following signals in its 'HI NMR spectrum (ppm): 1.06 (triplet, 3H), 2.12 (singlet, 3H), 2.45 (quartet, 2H); and the following signals in its "C NMR spectrum ( ppm): 7.6, 29.5, 36.8, 208.8. Draw the structure of the unknown compound. Click and drag to start drawing a structure. O 0 Ö 0:0 X G 0* @
An unknown compound has a molecular formula of C,H,O. Its IR spectrum shows prominent absorptions at 2980, 2960, and 1718 cm. It exhibits the following signals in its 'HI NMR spectrum (ppm): 1.06 (triplet, 3H), 2.12 (singlet, 3H), 2.45 (quartet, 2H); and the following signals in its "C NMR spectrum ( ppm): 7.6, 29.5, 36.8, 208.8. Draw the structure of the unknown compound. Click and drag to start drawing a structure. O 0 Ö 0:0 X G 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
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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