15. A compound, C7H14O, gives rise to the 13C and 1H NMR data shown below. Draw its structure. 13C NMR: 8 29.8, 30.9, 32.3, 56.0, 208.4 1H NMR: 8 1.02 (9H, singlet), 2.12 (3H, singlet), and 2.33 (2H, singlet)

15. A compound, C7H14O, gives rise to the 13C and 1H NMR data shown below. Draw its structure. 13C NMR: 8 29.8, 30.9, 32.3, 56.0, 208.4 1H NMR: 8 1.02 (9H, singlet), 2.12 (3H, singlet), and 2.33 (2H, singlet)

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

Chapter18: Functional Derivatives Of Carboxylic Acids

Section: Chapter Questions

Problem 18.18P: Propose a structural formula for each compound consistent with its 1H-NMR and 13C-NMR spectra. (a)...

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NMR Spectroscopy

NMR stands for Nuclear Magnetic Resonance in which the study of different molecules is done based on the interaction of radiofrequency electromagnetic radiations with the nuclei of molecules placed in a strong magnetic field. A precise study of spectra of visible light and all bands of electromagnetic radiation is called spectroscopy.

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15. A compound, C7H14O, gives rise to the 13C and 1H NMR data shown below. Draw its structure.
13C NMR: 8 29.8, 30.9, 32.3, 56.0, 208.4
1H NMR: 8 1.02 (9H, singlet), 2.12 (3H, singlet), and 2.33 (2H, singlet)

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