stable carbocation than but-2-ene. - When 1-methylcyclopentene undergoes an addition reaction with a carbocation intermediate, the carbocation will form on Carbon 5. - 3,3-diethylhex-1-ene will undergo rearrangement upon formation of a carbocation. - 3-methylcyclopentene will undergo rearrangement upon formation of a carbocation. - 1-ethylcyclopent-1-ene is the name of the product of reaction of 1-bromo-2-ethylcyclopentane with KOH in ethanol solvent
stable carbocation than but-2-ene. - When 1-methylcyclopentene undergoes an addition reaction with a carbocation intermediate, the carbocation will form on Carbon 5. - 3,3-diethylhex-1-ene will undergo rearrangement upon formation of a carbocation. - 3-methylcyclopentene will undergo rearrangement upon formation of a carbocation. - 1-ethylcyclopent-1-ene is the name of the product of reaction of 1-bromo-2-ethylcyclopentane with KOH in ethanol solvent
World of Chemistry, 3rd edition
3rd Edition
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Chapter20: Organic Chemistry
Section: Chapter Questions
Problem 4STP
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- 2-methylpropene produces the more stable carbocation than but-2-ene.
- When 1-methylcyclopentene undergoes an addition reaction with a carbocation intermediate, the carbocation will form on Carbon 5.
- 3,3-diethylhex-1-ene will undergo rearrangement upon formation of a carbocation.
- 3-methylcyclopentene will undergo rearrangement upon formation of a carbocation.
- 1-ethylcyclopent-1-ene is the name of the product of reaction of 1-bromo-2-ethylcyclopentane with KOH in ethanol solvent
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