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The carbon of cyanide acts as the nucleophile in this SN2 substitution reaction. The carbon attacks iodomethane at its carbon via backside attack (or opposite the side of iodine). It goes through a one step transition to achieve the final product of cyanomethane.

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Q: What is the mechanism for cyanide substituting into iodomethane?
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Related questions

Would chloromethane or iodomethane react faster?

Iodide is a better leaving group than chloride so iodomethane would react faster.


What is the chemical formula for Iodimethane?

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What is the name of the ion CN?

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