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Draw the most stable chair conformer of the most stable isomer of 1,3,5-trimethylcyclohexane.

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Which of the following illustrates an axial OH?


A) Which of the following illustrates an axial OH? A) B) C) D)
B) Which of the following illustrates an axial OH? A) B) C) D)
C) Which of the following illustrates an axial OH? A) B) C) D)
D) Which of the following illustrates an axial OH? A) B) C) D)

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

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Are the two substituents cis or trans? Are the two substituents cis or trans? A) trans B) cis C) neither


A) trans
B) cis
C) neither

D) None of the above
E) A) and C)

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Which of the following compounds are constitutional isomers?


A) Which of the following compounds are constitutional isomers? A) B) C) D)
B) Which of the following compounds are constitutional isomers? A) B) C) D)
C) Which of the following compounds are constitutional isomers? A) B) C) D)
D) Which of the following compounds are constitutional isomers? A) B) C) D)

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

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Draw the gauche conformer of the following compound looking down the indicated bond. Draw the gauche conformer of the following compound looking down the indicated bond.

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What is the IUPAC name of the following compound? What is the IUPAC name of the following compound? A) 2,5-diethylhexane B) 3,6-dimethyloctane C) 2-ethyl-5-methylheptane D) 2,5-dimethylheptane


A) 2,5-diethylhexane
B) 3,6-dimethyloctane
C) 2-ethyl-5-methylheptane
D) 2,5-dimethylheptane

E) B) and C)
F) B) and D)

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Which of the following is a gauche conformer?


A) Which of the following is a gauche conformer? A) B) C) D)
B) Which of the following is a gauche conformer? A) B) C) D)
C) Which of the following is a gauche conformer? A) B) C) D)
D) Which of the following is a gauche conformer? A) B) C) D)

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

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Which is the most stable chair conformer of the following compound? Which is the most stable chair conformer of the following compound? A) B) C) D)


A) Which is the most stable chair conformer of the following compound? A) B) C) D)
B) Which is the most stable chair conformer of the following compound? A) B) C) D)
C) Which is the most stable chair conformer of the following compound? A) B) C) D)
D) Which is the most stable chair conformer of the following compound? A) B) C) D)

E) C) and D)
F) B) and C)

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Which pair of the following compounds are constitutional isomers?


A) Which pair of the following compounds are constitutional isomers? A) B) C) D)
B) Which pair of the following compounds are constitutional isomers? A) B) C) D)
C) Which pair of the following compounds are constitutional isomers? A) B) C) D)
D) Which pair of the following compounds are constitutional isomers? A) B) C) D)

E) B) and D)
F) B) and C)

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Which of the following cycloalkanes has the most angle strain?


A) Which of the following cycloalkanes has the most angle strain? A) B) C) D)
B) Which of the following cycloalkanes has the most angle strain? A) B) C) D)
C) Which of the following cycloalkanes has the most angle strain? A) B) C) D)
D) Which of the following cycloalkanes has the most angle strain? A) B) C) D)

E) B) and D)
F) C) and D)

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Which of the following is the least stable chair conformer of the most stable isomer of 1-ethyl-2,4-dimethylcyclohexane?


A) Which of the following is the least stable chair conformer of the most stable isomer of 1-ethyl-2,4-dimethylcyclohexane? A) B) C) D)
B) Which of the following is the least stable chair conformer of the most stable isomer of 1-ethyl-2,4-dimethylcyclohexane? A) B) C) D)
C) Which of the following is the least stable chair conformer of the most stable isomer of 1-ethyl-2,4-dimethylcyclohexane? A) B) C) D)
D) Which of the following is the least stable chair conformer of the most stable isomer of 1-ethyl-2,4-dimethylcyclohexane? A) B) C) D)

E) A) and C)
F) C) and D)

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What is the correct stoichiometry of oxygen for the balanced oxidation reaction? What is the correct stoichiometry of oxygen for the balanced oxidation reaction?

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What is the correct stoichiometry of oxygen for the balanced oxidation reaction? What is the correct stoichiometry of oxygen for the balanced oxidation reaction?

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Draw both chair conformers of the following compound. Draw both chair conformers of the following compound.

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What are the structures and IUPAC names of all constitutional isomers of C6H14?

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Which is the least stable chair conformer of the following compound? Which is the least stable chair conformer of the following compound? A) B) C) D)


A) Which is the least stable chair conformer of the following compound? A) B) C) D)
B) Which is the least stable chair conformer of the following compound? A) B) C) D)
C) Which is the least stable chair conformer of the following compound? A) B) C) D)
D) Which is the least stable chair conformer of the following compound? A) B) C) D)

E) All of the above
F) None of the above

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Are the two substituents cis or trans? Are the two substituents cis or trans? A) trans B) cis C) neither


A) trans
B) cis
C) neither

D) A) and B)
E) A) and C)

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Draw the most stable chair conformer of the most stable isomer of 1,3,5-trimethylcyclohexane.

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Which is the least stable chair conformer of the following compound? Which is the least stable chair conformer of the following compound? A) B) C) D)


A) Which is the least stable chair conformer of the following compound? A) B) C) D)
B) Which is the least stable chair conformer of the following compound? A) B) C) D)
C) Which is the least stable chair conformer of the following compound? A) B) C) D)
D) Which is the least stable chair conformer of the following compound? A) B) C) D)

E) C) and D)
F) A) and D)

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What is the IUPAC name of the following compound? What is the IUPAC name of the following compound? A) 3-isopropyl-5-ethylheptane B) 2-methyl-3-ethyl-5-ethylheptane C) 3,5-diethyl-2-methylheptane D) 2-methyl-3,5-diethylheptane


A) 3-isopropyl-5-ethylheptane
B) 2-methyl-3-ethyl-5-ethylheptane
C) 3,5-diethyl-2-methylheptane
D) 2-methyl-3,5-diethylheptane

E) B) and C)
F) C) and D)

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