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Treatment of 1,2-dimethylcyclopentene with OsO4, followed by aqueous NaHSO3, produces which of the following: Oll O III OIV OV OI OH CH3 CH3 OH II OH CH3 OH CH3 III OH CH3 H CH3 CH3 H for IV "OH CH3 CH3 H "H CH3

Treatment of 1,2-dimethylcyclopentene with OsO4, followed by aqueous NaHSO3, produces which of the following: Oll O III OIV OV OI OH CH3 CH3 OH II OH CH3 OH CH3 III OH CH3 H CH3 CH3 H for IV "OH CH3 CH3 H "H CH3

Chemistry
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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### Question: **Treatment of 1,2-dimethylcyclopentene with OsO4, followed by aqueous NaHSO3, produces which of the following:** The structures of the compounds labeled I to V are as follows: - **I** - Two hydroxyl (OH) groups are attached to the carbon atoms at the 1 and 2 positions of a cyclopentene ring. - Each hydroxyl-bearing carbon also has a methyl group (CH3) attached, resulting in two CH3 groups opposite each other on the ring. - **II** - Two hydroxyl (OH) groups are attached on the 1 and 2 positions of a cyclopentene ring, similar to I. - The arrangement of the hydroxyl groups differs from structure I. - **III** - Two hydroxyl (OH) groups are attached on the 1 and 2 positions of a cyclopentane ring. - The relative positions of the hydroxyl groups differ from structures I and II. - **IV** - Two hydroxyl (OH) groups are attached on the 1 and 2 positions of a cyclopentane ring. - The arrangement of these is staggered differently from structures I, II, and III. - **V** - A compound with no hydroxyl groups. ### Options: - **II** - **III** - **IV** - **V** - **I** **Graphs/Diagrams Explanation:** There are five molecular structures shown as options I to V. - **I, II, III & IV**: Each of these contains a cyclopentane ring with varying positions and arrangements of hydroxyl (OH) and methyl (CH3) groups. - **V**: This structure, differs from others as it lacks any hydroxyl groups and includes two oppositely positioned methyl groups on the ring structure.
Transcribed Image Text:### Question: **Treatment of 1,2-dimethylcyclopentene with OsO4, followed by aqueous NaHSO3, produces which of the following:** The structures of the compounds labeled I to V are as follows: - **I** - Two hydroxyl (OH) groups are attached to the carbon atoms at the 1 and 2 positions of a cyclopentene ring. - Each hydroxyl-bearing carbon also has a methyl group (CH3) attached, resulting in two CH3 groups opposite each other on the ring. - **II** - Two hydroxyl (OH) groups are attached on the 1 and 2 positions of a cyclopentene ring, similar to I. - The arrangement of the hydroxyl groups differs from structure I. - **III** - Two hydroxyl (OH) groups are attached on the 1 and 2 positions of a cyclopentane ring. - The relative positions of the hydroxyl groups differ from structures I and II. - **IV** - Two hydroxyl (OH) groups are attached on the 1 and 2 positions of a cyclopentane ring. - The arrangement of these is staggered differently from structures I, II, and III. - **V** - A compound with no hydroxyl groups. ### Options: - **II** - **III** - **IV** - **V** - **I** **Graphs/Diagrams Explanation:** There are five molecular structures shown as options I to V. - **I, II, III & IV**: Each of these contains a cyclopentane ring with varying positions and arrangements of hydroxyl (OH) and methyl (CH3) groups. - **V**: This structure, differs from others as it lacks any hydroxyl groups and includes two oppositely positioned methyl groups on the ring structure.
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