1. 2. Ph 1. Ph 2 OH AlBrs a = Proton transfer b = Lewis acid/base c = Radical chain substitution NMe₂ H₂SO4 Ph Ph NMe₂ Tamoxifen anti (brest) cancer drug AlBr J Ph Ph C d = Radical chain addition e = Electrophilic addition f = E1 Elimination NMе₂ Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution iSN2 Nucleophilic substitution

1. 2. Ph 1. Ph 2 OH AlBrs a = Proton transfer b = Lewis acid/base c = Radical chain substitution NMe₂ H₂SO4 Ph Ph NMe₂ Tamoxifen anti (brest) cancer drug AlBr J Ph Ph C d = Radical chain addition e = Electrophilic addition f = E1 Elimination NMе₂ Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. g= E2 Elimination h = SN1 Nucleophilic substitution iSN2 Nucleophilic substitution

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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