<span>C. Static electricity. Except that electrons are never really at rest.</span>
Answer:The IUPAC name of compound would be Hex-3-yn-ol
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.
Answer: The correct option is C.
Explanation: Beta minus (
) decay is the decay in which a neutron is converted into proton and releases beta particle or generally known as electron.
There is an increase in the Atomic number because one protons is being formed.
In the case of beta-minus decay of phosphorous, the P-nucleus gets changed to Sulfur nucleus. The balanced Chemical equation for this process is:
![^{32}_{15}\textrm{P}\rightarrow ^{32}_{16}\textrm{S}+^0_{-1}\beta](https://tex.z-dn.net/?f=%5E%7B32%7D_%7B15%7D%5Ctextrm%7BP%7D%5Crightarrow%20%5E%7B32%7D_%7B16%7D%5Ctextrm%7BS%7D%2B%5E0_%7B-1%7D%5Cbeta)
Hence, the correct option is C.