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This equation shows the reaction of trans-2,3-dimethyloxirane with hydrogen chloride to form 3-chloro-2-butanol.
how many total stereoisomer are possible for 3-Chloro-2-butanol?
Given that opening of the epoxide ring in this reaction is stereoselective, provide the names of the only two isomeric products using IUPAC guidelines.
Product one: _______ 3-chloro-2-butanol
Product two: _______3-chloro-2-butanol

Respuesta :

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Answer:

Product one: (2S, 3R)-3-chloro-2-butanol

Product two: (3S, 2R)-3-chloro-2-butanol

Explanation:

The IUPAC  name of the products following IUPAC guidelines are :

Product one: (2S, 3R)-3-chloro-2-butanol

Product two: (3S, 2R)-3-chloro-2-butanol

attached below is a pictorial representation of the formation of the 3-chloro-2-butanol via backside attack of Nucleophile

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