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

Respuesta :

Answer:

Prop-1-yn-1-ide

Explanation:

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

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