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Quiz Submissions – Exam #2
Kelly Johnson (username: 75KJ922478)
Attempt 1
Written: Jun 15, 2020 12:00 PM – Jun 15, 2020 1:30 PM
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Chapter_02_Alkanes_and_Cycloalkanes
Which of the following is the most stable conformation of cis-1-isopropyl-3-methylcyclohexane?
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What is the IUPAC name of the following compound?
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cis-1-tert-butyl-2-methylcyclopentane
trans-1-tert-butyl-2-methylcyclopentane
trans-1-isopropyl-4-methylcyclopentane
cis-1-isopropyl-2-methylcyclopentane
Which of the following compounds can adopt a chair conformation in which there are no axial methyl
groups?
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trans-1,3-dimethylcyclohexane
cis-1,2-dimethylcyclohexane
cis-1,4-dimethylcyclohexane
cis-1,3-dimethylcyclohexane
Which of the following undergoes the most exothermic combustion?
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2,2,3,3-tetramethylbutane
Which of the following cycloalkanes has the largest heat of combustion per carbon atom?
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Which of the following substituted cyclohexanes has the greatest energy for ring flipping from the
conformation in which the substituent is axial to the one where it is equatorial?
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The Newman projection of the gauche conformation of 1,2-dichloroethane is shown below.
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The most stable conformation of an alkane occurs when carbon−carbon bonds are staggered and bulky
groups are anti.
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The following pairs of Newman projections represent the same compound but in differing conformations.
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The following Newman projection represents 2-methylhexane.
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The following structures represent, from left to right, a cis and a trans isomer.
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Match the Newman projection for the conformation of 2-methylbutane to the indicated position on the
potential energy diagram.
Conformation A is represented by Roman numeral ____.