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Exam 5: Stereoisomerism

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Question 41

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Draw the enantiomer of the following compound.

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Question 42

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Identify the relationship between these two structures.

A) diastereomers
B) enantiomers
C) identical
D) unrelated compounds

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Question 43

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Which of the following is the correct structure for the compound (S) -3-methylheptane.

Assign the following stereocenter as having the R or S absolute configuration.

Is the following alkene cis, trans, or neither?

Draw in the plane of symmetry in the following compound.

What is the relationship between the two structures shown?

Draw the Fischer projection of the following compound.

Which of the following is a correct Fischer projection of the following compound?

Assign the absolute configuration of the chirality center as R or S.

If a sample of carvone gives a specific rotation of 0 and the specific rotation of pure (R)-carvone is −61, what is the configuration of the unknown sample?

Locate the chirality center(s) in the following compound.

What is the relationship between the following two compounds?

Draw a diastereomer of the following compound.

Is the following alkene E, Z, or neither?

Redraw the structure below as a wedge-dash structure and label all stereocenters with their absolute configuration.

Rank the following from highest to lowest priority according to the Cahn-Ingold-Prelog system. I. -F II. -H III. -OH IV. -SH

How many possible stereoisomers are there for Crestor (rosuvastatin) , a medication used to reduce cholesterol?

Draw in the plane of symmetry in the following compound.

Provide an IUPAC name of the following compound.