To synthesize the following via a single-step $S_{N} 2$ reaction starting from an alkyl halide,

allyl fluoride is treaded with $K C N$ in a polar protic solvent

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allyl fluoride is treaded with $K C N$ in a polar aprotic solvent

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allyl chloride is treaded with $K C N$ in a polar protic solvent

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allyl chloride is treaded with $K C N$ in a polar aprotic solvent

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Solution

The correct option is D
allyl chloride is treaded with $K C N$ in a polar aprotic solvent

For good $S_{N} 2$ , a salt like $K C N$ is used with the following substrate in apolar aprotic solvent like DMSO:

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Similar questions

Assume you get to start with an alkyl halide. To synthesize the following via a single-step $S_{N} 2$ reaction,
which of the following options is appropriate ?

To synthesize the following via a single-step $S_{N} 2$ reaction starting from an alkyl halide,

Assume you get to start with an alkyl halide. To synthesize the following via a single-step $S_{N} 2$ reaction,
which of the following options is appropriate ?

To synthesize the given compound via an $S_{N} 2$ reaction, which of the following options is appropriate:

Observe the given compound.

Which of the following is best suited to synthesize the compound via an $S_{N} 2$ reaction?

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To synthesize the following via a single-step SN2 reaction starting from an alkyl halide,

The correct option is D allyl chloride is treaded with KCN in a polar aprotic solvent For good SN2, a salt like KCN is used with the following substrate in apolar aprotic solvent like DMSO:

To synthesize the following via a single-step $S_{N} 2$ reaction starting from an alkyl halide,

The correct option is D
allyl chloride is treaded with $K C N$ in a polar aprotic solvent

For good $S_{N} 2$ , a salt like $K C N$ is used with the following substrate in apolar aprotic solvent like DMSO: