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[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.

Chemistry
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
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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 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.
Transcribed Image Text:[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.
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