NO2NO2CI1.-NO2NO2OH2.+H2Ng = SN1 Nucleophilic substitutionh = SN2 Nucleophilic substitutionProton transferd = Electrophilic additiona =b = Lewis acid/baseEl Eliminatione =с —Radical chain substitutionf= E2 EliminationIdentify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i foryour answers.12.

The correct option is given as:

NO2 CI 1. NO2 `NO2 OH 2. H2N° a = Proton transfer d = Electrophilic addition g = Sn1 Nucleophilic substitution b = Lewis acid/base e = E1 Elimination h = SN2 Nucleophilic substitution c = Radical chain substitution f= E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers.

NO2 CI 1. NO2 `NO2 OH 2. H2N° a = Proton transfer d = Electrophilic addition g = Sn1 Nucleophilic substitution b = Lewis acid/base e = E1 Elimination h = SN2 Nucleophilic substitution c = Radical chain substitution f= E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers.

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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