2. Draw the product that results from the reaction shown in the scheme below. You should show the arrow pushing going from reactants to the product (hint: this is a concerted mechanism and there will be a single step here). You should only write the major diastereomer product, and if another enantiomer is formed you may simply write "+ enantiomer." Another hint: the preferred endo product will be formed from a transition state that has orbital overlap between the diene and the cyano (CN) group. NC I

2. Draw the product that results from the reaction shown in the scheme below. You should show the arrow pushing going from reactants to the product (hint: this is a concerted mechanism and there will be a single step here). You should only write the major diastereomer product, and if another enantiomer is formed you may simply write "+ enantiomer." Another hint: the preferred endo product will be formed from a transition state that has orbital overlap between the diene and the cyano (CN) group. NC I

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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Please answer the subparts 4, 5, 6 and 7. Please mention all the mechanism and needed reagents. Thanks
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Please also draw the two products from step 1 and the curved arrow notation for an SN2 reaction involving Br- in the final box, the final two structures formed after the SN2 reaction described in Step 2
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