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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

#SPJ4

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An unknown compound is found to have a molar mass of 392.16 g/mol. If the empirical formula is C2H5PF2, what is the molecular fo
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Answer:

C8H20P4F8

Explanation:

Molecular formula is based off a ratio of the molecular formula's molar mass divided by the empirical formula's molar mass.

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2(12.01) + 5(1.01) + 30.97 + 2(18.99) = 98.02

We then divide the molecular molar mass by the empirical molar mass.

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