[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-
[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-
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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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)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F78d3386d-6d53-402c-988d-2c02b5589a57%2F2b23be80-b0e3-4ad5-9abf-dd5910bf576a%2Fcsp00vs_processed.jpeg&w=3840&q=75)
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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