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Draw the meso isomer of the following compound. Draw the meso isomer of the following compound.

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Which of the following is the correct IUPAC name for the following structure? Which of the following is the correct IUPAC name for the following structure?   A) (S) -2-ethylhexane B) (S) -3-methylheptane C) (R) -2-ethylhexane D) (R) -3-methylheptane


A) (S) -2-ethylhexane
B) (S) -3-methylheptane
C) (R) -2-ethylhexane
D) (R) -3-methylheptane

E) A) and B)
F) A) and D)

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Is the following alkene cis,trans,or neither? Is the following alkene cis,trans,or neither?

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What is the relationship of the following two structures? What is the relationship of the following two structures?   A) Enantiomers B) Diastereomers C) Constitutional Isomers D) Identical


A) Enantiomers
B) Diastereomers
C) Constitutional Isomers
D) Identical

E) All of the above
F) B) and D)

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Convert the following structure into a Fischer projection. Convert the following structure into a Fischer projection.

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Assign the chiral center as R or S. Assign the chiral center as R or S.

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Convert the following Fischer projection into a wedge/dash drawing. Convert the following Fischer projection into a wedge/dash drawing.

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Locate the chiral centers in the following compound. Locate the chiral centers in the following compound.

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Is the following a meso compound? Is the following a meso compound?

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What is the % of the S enantiomer in a sample of carvone that has a specific rotation of 30,given that the specific rotation of R-carvone is -61?


A) 25.5%
B) 51%
C) 49%
D) 74.5%

E) A) and B)
F) A) and C)

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What is the relationship between the following two compounds? What is the relationship between the following two compounds?   A) Constitutional isomers B) Stereoisomers C) Identical D) Not isomers,different compounds entirely.


A) Constitutional isomers
B) Stereoisomers
C) Identical
D) Not isomers,different compounds entirely.

E) All of the above
F) B) and C)

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What is the specific rotation of a sample of carvone that is an equal mixture of the R and S enantiomers (R- carvone has a specific rotation of -61) ?


A) -61
B) 64
C) 0
D) 61

E) A) and B)
F) A) and C)

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Draw the meso isomer of the following compound. Draw the meso isomer of the following compound.

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What is the relationship between the following two compounds? What is the relationship between the following two compounds?   A) Constitutional isomers B) Stereoisomers C) Identical D) Not isomers,different compounds entirely.


A) Constitutional isomers
B) Stereoisomers
C) Identical
D) Not isomers,different compounds entirely.

E) All of the above
F) A) and C)

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What is the relationship between the following two compounds? What is the relationship between the following two compounds?   A) Constitutional isomers B) Stereoisomers C) Identical D) Not isomers,different compounds entirely.


A) Constitutional isomers
B) Stereoisomers
C) Identical
D) Not isomers,different compounds entirely.

E) B) and C)
F) A) and B)

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Draw all possible stereoisomers of 1,3,5-trichlorocyclohexane.

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Locate the chiral centers in the following compound. Locate the chiral centers in the following compound.

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Locate the chiral centers in the following compound. Locate the chiral centers in the following compound.

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Convert the following Fischer projection into a wedge/dash drawing. Convert the following Fischer projection into a wedge/dash drawing.

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What is the relationship between the following two compounds? What is the relationship between the following two compounds?   A) Constitutional isomers B) Stereoisomers C) Identical D) Not isomers,different compounds entirely.


A) Constitutional isomers
B) Stereoisomers
C) Identical
D) Not isomers,different compounds entirely.

E) A) and C)
F) B) and C)

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