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ioda
3 years ago
5

Draw the structural formula of the major product of the reaction of (S)-2,2,3-trimethyloxirane with MeOH, H . Use the wedge/hash

bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it.

Chemistry
1 answer:
Katarina [22]3 years ago
8 0

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 (CH_3OH) 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!

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