Answer:
(4) option is correct
Explanation:
Given that,
The conformation of 2-methyl-3-pentanol, as viewed along the C₂-C₃ bond.
We need to find the Newman structures
Using given structures
The structure of 2- methyl-3- pentanol is shown in figure.
Through C₂-C₃ carbon shown the structure of Newman projection in figure.
Here, carbon 2 is in front side and carbon 3 is in back side in the figure.
Hence, (4) option is correct.
Answer:
(S)-3-methoxy-3-methylbutan-2-ol
Explanation:
In this case, we have an <u>epoxide opening in acid medium</u>. The first step then is the <u>protonation of the oxygen</u>. Then the epoxide is broken to generate the most <u>stable carbocation</u>. The nucleophile (
) will attack the carbocation generating a new bond. Finally, the oxygen is <u>deprotonated</u> to obtain an ether functional group and we will obtain the molecule <u>(S)-3-methoxy-3-methylbutan-2-ol</u>.
See figure 1
I hope it helps!
If the battery was removed, the energy produced by the battery would not be able to continue its path along the circuit.
This statement would be best characterized by the law of conservation of momentum—choice C.