6. Draw out the mechanism of the final step(s) of each reaction scheme (i.e., mechanism that starts at the indicated intermediate (A-C) and ends in the final product N-benzyl-3- phenylpropanamide). Use curved arrows to indicate the flow of electrons. Be sure to show any intermediates that are formed along the way. Show any by-products besides the ones provided. Scheme 1: Acid Chloride Route 0: HN Ö: Many steps co2 -CO HCI

6. Draw out the mechanism of the final step(s) of each reaction scheme (i.e., mechanism that starts at the indicated intermediate (A-C) and ends in the final product N-benzyl-3- phenylpropanamide). Use curved arrows to indicate the flow of electrons. Be sure to show any intermediates that are formed along the way. Show any by-products besides the ones provided. Scheme 1: Acid Chloride Route 0: HN Ö: Many steps co2 -CO HCI

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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