23.)а.)correct mechanistic arrows, provide the step-by-step mechanism that shows how the followingSUBSTITUTION reactions proceed. Provide correct stereochemistry in the final product(s).Determine the anticipated SUBSTITUTION mechanism for the reaction below. UsingBrNaSCH3DMSOMechanismb.)mechanistic arrows, provide the step-by-step mechanism that shows how the following ELIIMINATIONreactions proceed. Provide correct stereochemistry in the final product(s).Determine the anticipated ELIIMINATION mechanism for the reaction below. Using correctBrNaOCH3acetone, heatMechanism

a) Here, substrate is secondary alkyl bromide and nucleophile is strongest that is NaSCH3 and…

NaSCH3 DMSO Mechanism Determine the anticipated ELIIMINATION mechanism for the reaction below. Using correct b.) mechanistic arrows, provide the step-by-step mechanism that shows how the following ELIIMINATION reactions proceed. Provide correct stereochemistry in the final product(s). ae NaOCH3 acetone, heat Mechanism

NaSCH3 DMSO Mechanism Determine the anticipated ELIIMINATION mechanism for the reaction below. Using correct b.) mechanistic arrows, provide the step-by-step mechanism that shows how the following ELIIMINATION reactions proceed. Provide correct stereochemistry in the final product(s). ae NaOCH3 acetone, heat Mechanism

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations

Section11.SE: Something Extra

Problem 37MP

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