
Jason S. answered 01/07/15
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Biology & Chemistry Tutor
A) In the first part of the reaction, the NaNH2 will act as a nucleophile, attacking the hydrogen on the triple bond and deprotonating the alkyne, yielding NH3 + CH3CC- (Alkyne carbanion) Na+
The CH3CC- will then act as a nucleophile, attacking the CH3Br and forcing the Br group to leave as an anion (Br-). This leaves the final product of CH3CCCH3 + Br- NA+ + NH3