When
Nucleophile (Alkoxide) reacts with Alkyl Halide (
Substrate), Ether (
product) is formed with the elimination of
Leaving group (Iodide in this case).
This is
SN² a nucleophilic substitution reaction which takes place in primary alkyl halides. Reaction is given as,
A fusion reaction takes place between carbon and another element. Neutrons are released, and a different element is formed. The different element is Lighter than helium.
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!
I would say the first three. But I'm not 100% sure. I'm truly sorry if it's wrong