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(10 pts) 7. Draw trans-1,2-dibromocyclopentane. Show how you would make this molecule from cyclopentane and any inorganic reagents (10 pts) 8. Determine the structure of compound E, whose NMR is shown below. The formula for E is C, H,,O·There are no broad signals in the IR at 3400 cm' and no strong bands near 1700 cm There is a signal in the IR at 3050 cm. Assign the NMR signals to the structure you propose. Compound E 7 Show transcribed image text (10 pts) 7. Draw trans-1,2-dibromocyclopentane. Show how you would make this molecule from cyclopentane and any inorganic reagents (10 pts) 8. Determine the structure of compound E, whose NMR is shown below. The formula for E is C, H,,O·There are no broad signals in the IR at 3400 cm' and no strong bands near 1700 cm There is a signal in the IR at 3050 cm. Assign the NMR signals to the structure you propose. Compound E 7
(10 pts) 7. Draw trans-1,2-dibromocyclopentane. Show how you would make this molecule from cyclopentane and any inorganic reagents (10 pts) 8. Determine the structure of compound E, whose NMR is shown below. The formula for E is C, H,,O·There are no broad signals in the IR at 3400 cm' and no strong bands near 1700 cm There is a signal in the IR at 3050 cm. Assign the NMR signals to the structure you propose. Compound E 7
Show transcribed image text (10 pts) 7. Draw trans-1,2-dibromocyclopentane. Show how you would make this molecule from cyclopentane and any inorganic reagents (10 pts) 8. Determine the structure of compound E, whose NMR is shown below. The formula for E is C, H,,O·There are no broad signals in the IR at 3400 cm' and no strong bands near 1700 cm There is a signal in the IR at 3050 cm. Assign the NMR signals to the structure you propose. Compound E 7 1
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Casey DurganLv2
26 May 2019
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