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R3NC12H19NO3+2R3NH+Br A Treotment of 2-amino-2-methylcyclohexanone with methyl 2,4-dibromobutanoate in the prosence of a nonnucleophilic base, R1N, involves two succossive SN2 reactions and gives compound A.

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R3NC12H19NO3+2R3NH+Br A Treotment of 2-amino-2-methylcyclohexanone with methyl 2,4-dibromobutanoate in the prosence of a nonnucleophilic base, R1N, involves two succossive SN2 reactions and gives compound A. Propose a structural formula for compound A. Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction. - Use the wedge/hash bond tools to indicate stereochemistry where it exists. - Only draw the reactants. Separate multiple reactants using the + sign from the drop-down menu. - If there is more than one possible combination of alkyl bromide and nucleophile, draw only one combination. - Do not inciude counter-ions, e.g., Na+,I, in your

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