SN2 Reaction between Acetylide Anion and Chloromethane

 

Acetylide anion, formed by deprotonation of the alkyne with a strong base (such as NaNH2) is a strong nucleophile and readily undergoes SN2 reactions with alkyl halides. In this example, acetylide anion displaces chloride from chloromethane to give propyne. Note the planar central carbon in the SN2 transition state.