A carbon NMR spectrum has peaks at & 113 (1), 60 (2), and 15 (3). The numbers in the parentheses indicate the number of attached protons to each of the carbon signals. Explain why each of the following structures is NOT consistent with this spectrum. CH2OCH3 OCH2CH3 CH3OCH2-C-H CH3CH,0-C-CH3 CH,OCH3 0-CH3

A carbon NMR spectrum has peaks at & 113 (1), 60 (2), and 15 (3). The numbers in the parentheses indicate the number of attached protons to each of the carbon signals. Explain why each of the following structures is NOT consistent with this spectrum. CH2OCH3 OCH2CH3 CH3OCH2-C-H CH3CH,0-C-CH3 CH,OCH3 0-CH3

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions

Section19.SE: Something Extra

Problem 87AP: The proton NMR spectrum for a compound with formula C10H12O2 is shown below. The infrared spectrum...

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