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5. Using curved arrows, draw the mechanism of both steps involved in the synthetic pathway to imidazole (5). H;C CH;Co0 NH,* H3C ENH H3C -N HN -H -H H3C- H H;C- `NH H3C- 1 2 4 5 6. Suggest a reasonable retrosynthetic approach to disconnect oxazole (1) and draw the mechanism of the forward Robinson-Gabriel reaction: H3C -N H3C `N- 1 ZI

5. Using curved arrows, draw the mechanism of both steps involved in the synthetic pathway to imidazole (5). H;C CH;Co0 NH,* H3C ENH H3C -N HN -H -H H3C- H H;C- `NH H3C- 1 2 4 5 6. Suggest a reasonable retrosynthetic approach to disconnect oxazole (1) and draw the mechanism of the forward Robinson-Gabriel reaction: H3C -N H3C `N- 1 ZI

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
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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5. Using curved arrows, draw the mechanism of both steps involved in the synthetic pathway to imidazole (5). H3C CH,Co0 NH,* H3C ENH H3C -N- HN -H H3C H3C- `NH H3C H 1 2 3 4 5 6. Suggest a reasonable retrosynthetic approach to disconnect oxazole (1) and draw the mechanism of the forward Robinson-Gabriel reaction: H3C -N H3C `N- 1
Transcribed Image Text:5. Using curved arrows, draw the mechanism of both steps involved in the synthetic pathway to imidazole (5). H3C CH,Co0 NH,* H3C ENH H3C -N- HN -H H3C H3C- `NH H3C H 1 2 3 4 5 6. Suggest a reasonable retrosynthetic approach to disconnect oxazole (1) and draw the mechanism of the forward Robinson-Gabriel reaction: H3C -N H3C `N- 1
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