Compound X has the molecular formula C6H10. X decolorizes bromine in carbon tetrachloride. X also shows IR absorption at about 3
1 answer:
Answer:
The correct answer is - option D. (check image)
Explanation:
Alkynes and alkenes both decolorized bromine in carbon tetrachloride. The absorption of the IR at about 3300 cm-1 for the X here that are found in the terminal alkynes absorption range only. In presence of excess hydrogen and a nickel catalyst, x gives the 2-methyl pentane.
The most likely structure for X is: CH3-CH3-ch-CH2-C≡CH
You might be interested in
Answer:
The equations are
1)
2)
Explanation:
There are two ionization steps in the dissociation of hydroselenic acid.
In first dissociation the H₂Se loses one proton and forms hydrogen selenide ion as shown below:
The next step is again removal of a proton from the base formed above.
Answer:
Explanation:
Hello,
In this case, we are asked to compute the by mass percent representing the toxicity of ethylene glycol in the body mass. In such a way, since the by mass percent is computed with the shown below formula:
We can use the given masses to obtain:
Best regards.