Answer:
The final product of the reaction is (2S,3S)-2-ethoxy-3-methylpentane.
Explanation:
The given reaction undergoes [tex]S_{N}2[/tex] mechanism in which the nucleophile attacks the backside and it is substituted by the elimination of bromine.
Due to the backside attack of nucleophile , the inverse in stereo-chemistry is observed.
After the substitution of ethoxy group, the configuration is assigned according to the priority it shows clock wise direction(R) - configuration.
When hydrogen faces the front side , it results shows inverse configuration i.e, S- configuration.
The chemical reaction is as follows.
