Compound A has a molecular formula C5H11NO and a HNMR spectrum as such: 8.05 (s, 1H), 3.04 (s, 3H), 2.67 (t, 2H), 1.55 (m, 2H), 0.91 (t, 3H). The CNMR shows one peak above 160ppm. When hydrolyzed with H3O+, two compounds are formed B and C after aqueous workup. Draw the structures of A, B, and C.
Compound A has a molecular formula C5H11NO and a HNMR spectrum as such: 8.05 (s, 1H), 3.04 (s, 3H), 2.67 (t, 2H), 1.55 (m, 2H), 0.91 (t, 3H). The CNMR shows one peak above 160ppm. When hydrolyzed with H3O+, two compounds are formed B and C after aqueous workup. Draw the structures of A, B, and C.
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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Compound A has a molecular formula C5H11NO and a HNMR spectrum as such: 8.05 (s, 1H), 3.04 (s, 3H), 2.67 (t, 2H), 1.55 (m, 2H), 0.91 (t, 3H). The CNMR shows one peak above 160ppm. When hydrolyzed with H3O+, two compounds are formed B and C after aqueous workup. Draw the structures of A, B, and C.
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