Chemistry1.2.ů.+1.CH₂OHa= Proton transferb= Lewis acid/basec = Radical chain substitutiond Radical chain addition=2.AqueousacetoneOCH₂+Y HOe Electrophilic additionf E1 Eliminationg = E2 EliminationHCIIdentify the mechanism by which each of the reactions above proceeds from among themechanisms listed. Use the letters a- j for your answers.h= S1 Nucleophilic substitutioni= SN2 Nucleophilic substitutionj= Electrophilic aromatic substitution

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1. 2. of 1.. Å 2. + CH₂OH a= Proton transfer b= Lewis acid/base c= Radical chain substitution d= Radical chain addition Aqueous acetone OCH T e Electrophilic addition f= E1 Elimination g = E2 Elimination . HCI на h= S1 Nucleophilic substitution i= SN2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a- j for your answers. j Electrophilic aromatic substitution M

1. 2. of 1.. Å 2. + CH₂OH a= Proton transfer b= Lewis acid/base c= Radical chain substitution d= Radical chain addition Aqueous acetone OCH T e Electrophilic addition f= E1 Elimination g = E2 Elimination . HCI на h= S1 Nucleophilic substitution i= SN2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a- j for your answers. j Electrophilic aromatic substitution M

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter10: Organohalides

Section10.SE: Something Extra

Problem 45AP

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