2. For each of the nucleophilic substitution reactions below (a-d), place a box around the most nucleophilic atom, circle the most electrophilic atom, and draw a straight arrow to point to the leaving group. Then predict the main carbon containing product of each reaction, drawing its line structure showing stereochemistry using wedges and dashes, if appropriate. Predict the type of mechanism: circle SN1 or SN2. a. b. C. d. e. Br O + Na CEN Θ Θ CI + Na N=N=N (NaN3) Zo. H I + O-H + Sigla Na + CH3 + TH= Na S-CH3 Br Ἡ water SN2 SN1 SN² SN1 SN2 SN1 SN2 SN1 SN2 SN1

2. For each of the nucleophilic substitution reactions below (a-d), place a box around the most nucleophilic atom, circle the most electrophilic atom, and draw a straight arrow to point to the leaving group. Then predict the main carbon containing product of each reaction, drawing its line structure showing stereochemistry using wedges and dashes, if appropriate. Predict the type of mechanism: circle SN1 or SN2. a. b. C. d. e. Br O + Na CEN Θ Θ CI + Na N=N=N (NaN3) Zo. H I + O-H + Sigla Na + CH3 + TH= Na S-CH3 Br Ἡ water SN2 SN1 SN² SN1 SN2 SN1 SN2 SN1 SN2 SN1

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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