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Exam 5: Stereoisomerism

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Question 41

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Draw a diastereomer 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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Draw in the plane of symmetry in the following compound.

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

What is the relationship between the two structures shown?

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

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

Draw the Fischer projection of the following compound.

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

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?

Is the following alkene cis, trans, or neither?

Draw the enantiomer of the following compound.

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

Draw in the plane of symmetry in the following compound.

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

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

Provide an IUPAC name of the following compound.

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

What is the relationship between the following two compounds?

Is the following alkene E, Z, or neither?