Answer:The IUPAC name of compound would be Hex-3-yn-ol
Step-by-step explanation:
When butyne is treated with LDA it leads to generation of carbanion on the terminal alkyne.
As LDA is disopropyl amide which happens to be quite a good base and hence it is sufficiently basic to abstract the acidic proton on the terminal alkyne.
So this proton abstraction leads to generation of a carbanion which can now acts as a nucleophile in step 2.
In step 2 the generated carbanion attacks the strained epoxide ring to open the strained epoxide ring .The product of step 2 leads to generation of hex-3-yn-1-olate
Further on treating the product formed in step 2 with the dilute acid it leads to the formation of alcohol as the negative charge on oxygen can now be neutralised.
Kindly refer the mechanism for structure of compounds.