Show how you might synthesize this compound from an alkyl bromide and a nucleophile in an SN2 reaction. N3 • 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 include counter-ions, e.g., Na", I", in your answer.

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To synthesize this compound from an alkyl bromide: The 3-bromo-2-methylpentane is the alkyl bromide and azide is the nucleophile.

How to synthesize the compound from an alkyl bromide and a nucleophile in an SN2 reaction?

The bromine leaving group initiates the reaction, which is then followed by an assault on the electrophilic carbon at the bromine leaving site by the nucleophile azide.

In this reaction, azide and alkyl bromide mix to form the desired product using the SN2 mechanism. Through a coordinated process, the bromine atom is simultaneously removed and sodium azide, acting as a nucleophile, attacks the carbon-containing bromine group to produce the SN2 product.

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