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What set of reaction conditions would favor an sn2 reaction on 2-bromo-3-methylbutane?

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The set of reaction conditions would favor a sn2 reaction on 2-bromo-3-methylbutane is a strong nucleophile in an aprotic solvent. The correct option is D.

What is Sn2 reactions?

It is a type of nucleophilic substitution reaction. This mechanism is common in organic chemistry. In these reactions, one bond is break and one bond is formed simultaneously.

The sn2 is a nucleophile reaction, and it is a strong nucleophile. This type of reaction, will occur in the compounds in which there is one alkyl halide group and a good leaving group.

In 2-bromo-3-methylbutane, there is a bromine and methyl group both, so the favor would be a strong nucleophile in an aprotic solvent.

Thus, the correct option is D) strong nucleophile in an aprotic solvent.

To learn more about Sn2 reactions, refer to the link:

https://brainly.com/question/27548297

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The question is incomplete. Your complete question is given below:

A) weak nucleophile in a protic solvent

B) weak nucleophile in an aprotic solvent

C) strong nucleophile in a protic solvent

D) strong nucleophile in an aprotic solvent

E) none of the above

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