2 Cn A Proton Transfer B Lewis Acid Base C Radical Chain Substitution Dmso D Electrophilic Addition E E1 Eliminatio 1 (21.15 KiB) Viewed 19 times
2 Cn A Proton Transfer B Lewis Acid Base C Radical Chain Substitution Dmso D Electrophilic Addition E E1 Eliminatio 2 (23.24 KiB) Viewed 19 times
2. . CN a Proton transfer b= Lewis acid/base c= Radical chain substitution DMSO d Electrophilic addition e E1 Elimination. f = E2 Elimination KBr 9= SN1 Nucleophilic substitution h= SN2 Nucleophilic substitution B Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters ai for your answers. 1. 2.
1. 2. ty OE! N(CH₂) a Proton transfer b= Lewis acid/base c = Radical chain substitution 2. [Review Topics] + d= Electrophilic addition e E1 Elimination. f= E2 Elimination [References] HN(CH₂), Cl OEt NaBr g= SN1 Nucleophilic substitution h = SN2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a- i for your answers. 1.
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