[References The mass spectrum of compound A shows the molecular lon at m/z 85, an M + 1 peak at m/z 86 of approximately 6% abundance relative to M, and an M + 2 peak at m/z 87 of less than 0.1% abundance relative to M. Assuming that compound A has only C, H, and one N atoms, determine the molecular formula, and then draw a possible structure if compound A has an IR absorption at 1620-1680 cm 1, 2 absorptions at 3280-3450 cm¹, and a (q, 1H) absorption at 4.6-5.7 8 in the ¹H-NMR spectrum.

[References The mass spectrum of compound A shows the molecular lon at m/z 85, an M + 1 peak at m/z 86 of approximately 6% abundance relative to M, and an M + 2 peak at m/z 87 of less than 0.1% abundance relative to M. Assuming that compound A has only C, H, and one N atoms, determine the molecular formula, and then draw a possible structure if compound A has an IR absorption at 1620-1680 cm 1, 2 absorptions at 3280-3450 cm¹, and a (q, 1H) absorption at 4.6-5.7 8 in the ¹H-NMR spectrum.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter12: Structure Determination: Mass Spectrometry And Infrared Spectroscopy

Section12.SE: Something Extra

Problem 48AP: The infrared spectrum of the compound with the mass spectrum shown below lacks any significant...

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