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. 8 1. 2. (CH3)3 COH + (CH3)3CMaBr (CH3), comgBr + Mechanism: (CH3)3c0JH + (CH3)3 cm (CH3)3 CH γ Mechanism: 3. CH3C CH CHO + H CH3MgBr + NaN H2 + Mechanism: CH3 C = GJ H Mechanism: 5' BF3 Mechanism: CO2 CH3 Jmg Br + NGÀNH, Omg Br C-H CHB CH3C=C-Na + инзт Li + cooli ༠༠; CH3OCH3 F3B

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. 8 1. 2. (CH3)3 COH + (CH3)3CMaBr (CH3), comgBr + Mechanism: (CH3)3c0JH + (CH3)3 cm (CH3)3 CH γ Mechanism: 3. CH3C CH CHO + H CH3MgBr + NaN H2 + Mechanism: CH3 C = GJ H Mechanism: 5' BF3 Mechanism: CO2 CH3 Jmg Br + NGÀNH, Omg Br C-H CHB CH3C=C-Na + инзт Li + cooli ༠༠; CH3OCH3 F3B

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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