please help with this question. thank you. Given that compound X has a molecular formula of C6H10O2, gave three peaks in its 13C NMR spectrum (14, 63 and 158 ppm) and two peaks in its 1H NMR spectrum (1.4 ppm, triplet and 4.3 ppm, quartet), provide a structure for compound X and briefly explain.

please help with this question. thank you. Given that compound X has a molecular formula of C6H10O2, gave three peaks in its 13C NMR spectrum (14, 63 and 158 ppm) and two peaks in its 1H NMR spectrum (1.4 ppm, triplet and 4.3 ppm, quartet), provide a structure for compound X and briefly explain.

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

Chapter17: Carboxylic Acids

Section: Chapter Questions

Problem 17.17P

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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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please help with this question. thank you.

Given that compound X has a molecular formula of C6H10O2, gave three peaks in its 13C NMR spectrum (14, 63 and 158 ppm) and two peaks in its 1H NMR spectrum (1.4 ppm, triplet and 4.3 ppm, quartet), provide a structure for compound X and briefly explain.

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