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Chapter 6: Q100P (page 287)

What stereoisomers are obtained when (S)-3-methyl-1-pentene reacts with Cl2?

Short Answer

Expert verified

The formation of the stereoisomer is trans-1,2dichloro-(S)-3-methyl- pentane.

Step by step solution

01

Definition of stereoisomers

Stereoisomers are those which has the same linkage with the main group but their orientation is space are different.

02

Reaction mechanism

The structure of parent molecule is S. so it is given by,

So, the formation of the product is trans-1,2dichloro-(S)-3-methyl- pentane.

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Most popular questions from this chapter

eDraw structures for the following:

a. 2-propyloxirane

b. cyclohexene oxide

c. 2,2,3,3-tetramethyloxirane

d. 2,3-epoxy-2-methylpentane

a. How many s bond orbitals are available for overlap with the vacant p orbital in the methyl cation?

b. Which is more stable: a methyl cation or an ethyl cation? Why?

What reagents are needed to synthesize the following alcohols?

What aspect of the structure of the alkene does ozonolysis not tell you ?

What stereoisomers would you expect to obtain from each of the following reactions
See all solutions

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