BUCINm ol compound A shows the molecular ion at mz 85, an M+1 peak at m 86 of appeoximately 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, detennine 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 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.

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ihe mass spectrum of compound A shows the inolecular ion at mz 85, an M 1 peak at m 86 of approximately 6% abundance relative to M, and an M2 pcak at m
87 of less than 0.1% abundance relative to M.
Assuming that compound A has only C, H, and one N atoms, detennine the molecular formula, and then draw a possible structure if copound A has IR absorptinn
at 1620-1680 cm but not at 3010-3090 cm.
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.
O IF
ChemDoodle
Neat
Transcribed Image Text:ihe mass spectrum of compound A shows the inolecular ion at mz 85, an M 1 peak at m 86 of approximately 6% abundance relative to M, and an M2 pcak at m 87 of less than 0.1% abundance relative to M. Assuming that compound A has only C, H, and one N atoms, detennine the molecular formula, and then draw a possible structure if copound A has IR absorptinn at 1620-1680 cm but not at 3010-3090 cm. 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. O IF ChemDoodle Neat
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