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1 | |
CH2CH(CH2)4CH3 is: |
| | A) | 2-Hexene |
| | B) | cis-2-Heptene |
| | C) | 1-Methylcyclohexene |
| | D) | 1-Heptene |
| | E) | 1-Heptyne |
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2 | |
Cis-2-hexene is an isomer of which of the following: |
| | A) | Hexane |
| | B) | 2-Methylpentane |
| | C) | 1-Methylcyclopentane |
| | D) | 1-Methylcyclohexane |
| | E) | None of the above |
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3 | |
When 2,3-dimethyl-2-butene is exposed to hydrogen gas under pressure with a Ni catalyst the product is: |
| | A) | Hexane |
| | B) | 3-Hexyne |
| | C) | 2,3-Dimethylbutane |
| | D) | trans-1,2-Dimethylcyclobutane |
| | E) | cis-1,2-Dimethylcyclobutane |
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4 | |
Which of the following when exposed to chlorine will produce 2,3-dichloropentane? |
| | A) | cis-2-Pentene |
| | B) | Pentane |
| | C) | 1-Pentyne |
| | D) | Cyclopentane |
| | E) | 1,2-Dichlorohexane |
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5 | |
Trans-2-hexene when reacted with chlorine produces |
| | A) | cis-2-Hexene |
| | B) | Hexane |
| | C) | 2,3-Dichlorohexane |
| | D) | 1-Hexane |
| | E) | 1,2-Dichlorohexane |
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6 | |
Which of the following substance will cause bromine to lose its color? |
| | A) | Pentane |
| | B) | Cyclopentane |
| | C) | 1-Methylcyclopentane |
| | D) | cis-2-Pentene |
| | E) | None of the above |
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7 | |
An alkene exposed to water and an acid catalyst produces |
| | A) | An alkane |
| | B) | An alkyne |
| | C) | An aromatic compound |
| | D) | An alcohol |
| | E) | None of the above |
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8 | |
2-Butene treated with potassium permanganate produces: |
| | A) | Butanoic acid |
| | B) | 2-Butyne |
| | C) | 2-Butanol |
| | D) | 2,3-Butandiol |
| | E) | Butanoic acid |
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9 | |
An alkene was treated with potassium permanganate to produce 3,4-heptandiol. What was original alkene? |
| | A) | 2-Butene |
| | B) | 3-Hexene |
| | C) | 3-Heptene |
| | D) | 2-Heptene |
| | E) | None of the above |
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10 | |
An alkene exposed to water and acid produced octan-3-ol and octan-4-ol. What was the starting alkene? |
| | A) | cis and/or trans-3-octanol |
| | B) | cis and/or trans 4-octanol |
| | C) | cis and/or trans 2-octanol |
| | D) | A and B |
| | E) | A and C |
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