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Chapter 4: Q.4-29E (page 114)

Draw a stereoisomer of trans-1, 3-dimethylcyclobutane.

Short Answer

Expert verified

There is only one stereoisomer of trans-1, 3-dimethylcyclobutane.

Step by step solution

01

Definition of stereoisomers

Stereoisomers are the isomers that have the same connectivity but difference in the spatial arrangement of atoms in space.

There are two types of stereoisomers enantiomers and diastereomers. Enantiomers are the stereoisomers that are the mirror images of each other while diastereomers are not mirrored images of each other.

02

Different stereoisomers of trans-1, 3-dimethylcyclobutane

There is only one stereoisomer of trans-1, 3-dimethylcyclobutane which is cis-1, 3-dimethylcyclobutane. It is shown as follow;

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Most popular questions from this chapter

In light of your answer to Problem 4-48, draw the two chair conformations of 1,1,3-trimethylcyclohexane and estimate the amount of strain energy in each. Which conformation is favored?

Draw two different chair conformations of trans-1,4 dimethylcyclohexane, and label all positions as axial or equatorial.

A 1, 2-cis disubstituted cyclohexane, such as cis-1, 2-dichlorocyclohexane, must have one group axial and one group equatorial. Explain.

Galactose, a sugar related to glucose, contains a six-membered ring in which all the substituents except the-OH group, indicated below in red, are equatorial. Draw galactose in its more stable chair conformation.

Why do you suppose an axial cyano (鈥揅N) substituent causes practically no 1,3-diaxial steric strain (0.4 kJ/mol)? Use molecular models to help with your answer.
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