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