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timurjin [86]
2 years ago
13

Ethyl (r)-4-phenylhexanoate was treated with ethyl lithium followed by acid hydrolysis (to neutralize). How many stereoisomers o

f the resulting alcohol were formed?
Chemistry
1 answer:
Oksanka [162]2 years ago
4 0

3 stereoisomers of the resulting alcohol were formed when Ethyl (r)-4-phenylhexanoate was treated with ethyl lithium followed by acid hydrolysis (to neutralize).

<h3>Stereoisomers:</h3>

In contrast to atomic connection, stereoisomers differ in the spatial arrangement of their atoms. The mirror-image stereoisomers, a non-superimposable pair of two molecules that are mirror images of one another, are one of their most intriguing types of isomers.

These include non-enantiomeric optical isomers, cis-trans isomers, E-Z isomers, and meso compounds. Rarely do diastereomers share the same physical characteristics. Stereoisomers are isomers that share the same structure (i.e., the same pieces), but differ in how those parts are arranged in space.

Stereoisomers are isomers that share the same structure (i.e., the same pieces), but differ in how those parts are arranged in space.

Learn more about stereoisomers here:

brainly.com/question/18120547

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<h3>What is the boiling point?</h3>

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