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balu736 [363]
3 years ago
12

Draw the organic product formed when the structure shown below undergoes a reaction with nanh2. there is no aqueous workup in th

is reaction.

Chemistry
1 answer:
blagie [28]3 years ago
5 0

Answer:

Prop-1-yn-1-ide

Explanation:

In this case, we will have an <u>acidic hydrogen</u> upon the left carbon in the alkyne. In the presence of a<u> base</u>, we can <u>remove</u> this hydrogen. In this reaction the base will be NH_2^-. The <u>amidure ion</u> will remove the hydrogen of the alkyne to produce a <u>carboanion</u>. (See figure)

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