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Draw all possible stereoisomers for each compound. Label pairs of enantiomers and diastereomers.

a.

b.

c.

Short Answer

Expert verified

a. The A and B pair are diastereomers. The B and C pair are enantiomers.

b. The A and B, and C and D pairs are enantiomers. The A and C, A and D, B and C, B and D are diastereomers.

c. The A and B pair are diastereomers.

Step by step solution

01

Stereoisomers  

The count of stereoisomers can be calculated by the chiral centers. The more the number of chiral centers, the more will be the stereoisomers.

The formula to calculate stereoisomers is: , where n is the count of chiral center.

02

Enantiomers and diastereomers

If the stereoisomers have the mirror images non-superimposable and, therefore, they have opposite configurations (R isomer and S isomer), then the isomers are termed as enantiomers.

If the stereoisomers are not associated with any kind of mirror image, and they have cis-trans geometry then, the isomers are termed as diastereomers.

03

Explanation

a. The molecule has two chiral centers due to the presence of four different groups at each chiral center.

One cis molecule and one trans molecule can be drawn. The cis molecule has a plane of symmetry due to the presence of two methyl groups above the plane. The trans molecule has its enantiomer because there is no plane of symmetry.

Therefore, the number of stereoisomers is three.

  • The A and B pair are diastereomers.
  • The B and C pair are enantiomers.

Stereoisomers

b. The molecule has two chiral centers due to the presence of four different groups at each chiral center. Therefore, it should have four stereoisomers maximum.

One cis molecule and one trans molecule can be drawn. The cis molecule has its enantiomers due to the absence of any plane of symmetry (methyl and OH groups are there).

The trans molecule has its enantiomer because there is no plane of symmetry.

Therefore, the number of stereoisomers is four.

  • The A and B, C, and D pairs are enantiomers due to opposite configurations or non-superimposable mirror images.
  • The A and C, A and D, B and C, B and D are diastereomers due to cis and trans geometry.

Stereoisomers

Stereoisomers

c. The molecule has two chiral centers due to the presence of four different groups at each chiral center.

One cis molecule and one trans molecule can be drawn. The cis molecule has a plane of symmetry due to the presence of two chloride groups above the plane.

The trans molecule also has a plane of symmetry due to the presence of two chloride groups.

Therefore, the number of stereoisomers is two.

  • The A and B pair are diastereomers.

Stereoisomers

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Most popular questions from this chapter

What is the maximum number of stereoisomers possible for a compound with:

a. three stereogenic centers;

b. eight stereogenic centers?

A molecule is achiral if it has a plane of symmetry in any conformation. Each of the following conformations does not have a plane of symmetry, but rotation around a carbonโ€“carbon bond forms a conformation that does have a plane of symmetry. Draw this conformation for each molecule.

a.

b.

Label each pair of compounds as constitutional isomers, stereoisomers, or not isomers of each other.

The amino acid (S)-alanine has the physical characteristics listed under the structure.

a. What is the melting point of (R)-alanine?

b. How does the melting point of a racemic mixture of (R)- and (S)-alanine compare to the melting point of (S)-alanine?

c. What is the specific rotation of (R)-alanine, recorded under the same conditions as the reported rotation of (S)-alanine?

d. What is the optical rotation of a racemic mixture of (R)- and (S)-alanine?

e. Label each of the following as optically active or inactive: a solution of pure (S)-alanine; an equal mixture of (R)- and (S)-alanine; a solution that contains 75% (S)- and 25% (R)-alanine.

The shrub ma huang (Section 5.4 A) contains two biologically active stereoisomers-ephedrine and pseudoephedrine-with two stereogenic centers as shown in the given structure. Ephedrine is one component of a once popular combination drug used by body builders to increase energy and alertness, while pseudoephedrine is a nasal decongestant.

a. Draw the structure of naturally occurring (โ€“)-ephedrine, which has the 1R,2Sconfiguration.

b. Draw the structure of naturally occurring (+)-pseudoephedrine, which has the 1S,2Sconfiguration.

c. How are ephedrine and pseudoephedrine related?

d. Draw all other stereoisomers of (โ€“)-ephedrine and (+)-pseudoephedrine and give the R,Sdesignation for all stereogenic centers.

e. How is each compound drawn in part (d) related to (โ€“)-ephedrine?

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