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2 answers:
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Answer:
See answer below
Explanation:
The picture below will show you the final product and mechanism.
In the first step, the NaNH₂ is a strong base, so, this base will substract the hydrogen from carbon 2, to generate a negative charge there, and then, carbon 2 becomes a nucleophyle.
As a nucleophyle it will attack to the CH₃I in the next step, and it will attach to the CH₃.
The second step is just a regular step to reduce the triple bond of the alkyne to alkane or alkene, this will depend on the quantity of the reactant. In this case, an alkene.
Hope this helps,,,,,,k
