[References] The mass spectrum of compound A shows the molecular ion 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/= 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 nas a 5-membered ring. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If more than one structure fits the description, draw them all. • Separate structures with + signs from the drop-down menu. opy aste ChemDoodle 10 42 98% 3/2-

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Chapter1: Chemical Foundations
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[References]
The mass spectrum of compound A shows the molecular ion 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 a 5-membered ring.
• You do not have to consider stereochemistry.
• You do not have to explicitly draw H atoms.
• If more than one structure fits the description, draw them all.
Separate structures with + signs from the drop-down menu.
C
opy aste
1.
ChemDoodle
10:3
98%
3/24)
Transcribed Image Text:ome O YouTube Translate Open Vellum Course Home [References] The mass spectrum of compound A shows the molecular ion 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 a 5-membered ring. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If more than one structure fits the description, draw them all. Separate structures with + signs from the drop-down menu. C opy aste 1. ChemDoodle 10:3 98% 3/24)
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