nucleophile: e-donor electrophile: E acceptor Q. No. IV). organometallics are always nucleophiles Predict the products for each of the following reactions. Indicate a rational mechanism in each case. Label each reactant as a nucleophile or an electrophile. 5. 1. 2. (CH3)3 COH + (CH3)3CMaBr (CH3)3c0mgBr Mechanism: + (CH3)3c0JH + (CH3)3c-mg B (CH3)3 CH Mechanism: CHO 3. CH,C CH + + H CH3MgBr NaN H2 + Mechanism: CH3 C = GJ H Li Mechanism: BF3 Mechanism: L-A CO2 + CH3Jmg Br omgBr Ç-H сна CH3C=C-Na + NGÀNH, NH3T ༠༠; CH3 CH3OCH3

nucleophile: e-donor electrophile: E acceptor Q. No. IV). organometallics are always nucleophiles Predict the products for each of the following reactions. Indicate a rational mechanism in each case. Label each reactant as a nucleophile or an electrophile. 5. 1. 2. (CH3)3 COH + (CH3)3CMaBr (CH3)3c0mgBr Mechanism: + (CH3)3c0JH + (CH3)3c-mg B (CH3)3 CH Mechanism: CHO 3. CH,C CH + + H CH3MgBr NaN H2 + Mechanism: CH3 C = GJ H Li Mechanism: BF3 Mechanism: L-A CO2 + CH3Jmg Br omgBr Ç-H сна CH3C=C-Na + NGÀNH, NH3T ༠༠; CH3 CH3OCH3

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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