The mass spectrum of compound A shows the molecular lon at miz 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 IR absorption at 1620-1680 cm but not at 3010-3090 cm

Organic Chemistry
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ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter17: Alcohols And Phenols
Section17.SE: Something Extra
Problem 55AP: A compound of unknown structure gave the following spectroscopic data: Mass spectrum: M+=88.1 IR:...
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The mass spectrum of compound A shows the molecular lon at mz 85, an M+1 peak at m/2 86 of approximately 6% abundance relative to M, and an M+ 2 peak at m/e 87 of
less than 0.19% abundance relative to M.
Assuming that compound A has only C, H, and one Natoms, determine the molecular formula, and then draw a possible structure if compound A has IR absorption at
1620-1680 cm but not at 3010-3090 cm1.
• You do not have to consider stereochemistry.
• You do not have to explicitly draw H atoms
• Il more than one structure fits the description, draw them al.
• Separate structures with + signs from the drop-down menu.
Chemboodie
Transcribed Image Text:The mass spectrum of compound A shows the molecular lon at mz 85, an M+1 peak at m/2 86 of approximately 6% abundance relative to M, and an M+ 2 peak at m/e 87 of less than 0.19% abundance relative to M. Assuming that compound A has only C, H, and one Natoms, determine the molecular formula, and then draw a possible structure if compound A has IR absorption at 1620-1680 cm but not at 3010-3090 cm1. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms • Il more than one structure fits the description, draw them al. • Separate structures with + signs from the drop-down menu. Chemboodie
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