8.3 What product would you obtain from catalytic hydrogenation of the following alkene? H₂ Pd/C

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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**8.3 What product would you obtain from catalytic hydrogenation of the following alkene?**

The image shows a chemical reaction involving an alkene undergoing catalytic hydrogenation. The starting molecule is a five-membered carbon ring (cyclopentene) with a double bond and two alkyl substituents attached, represented by lines extending from the ring.

The reaction is carried out in the presence of hydrogen gas (H₂) and a palladium on carbon (Pd/C) catalyst. The arrow indicates the conversion of the starting compound under these conditions.

Catalytic hydrogenation typically converts alkenes to alkanes by adding hydrogen across the double bond, resulting in a saturated compound without any double bonds. The reaction will yield a cyclopentane with two alkyl groups attached, replacing the double bond with single bonds.
Transcribed Image Text:**8.3 What product would you obtain from catalytic hydrogenation of the following alkene?** The image shows a chemical reaction involving an alkene undergoing catalytic hydrogenation. The starting molecule is a five-membered carbon ring (cyclopentene) with a double bond and two alkyl substituents attached, represented by lines extending from the ring. The reaction is carried out in the presence of hydrogen gas (H₂) and a palladium on carbon (Pd/C) catalyst. The arrow indicates the conversion of the starting compound under these conditions. Catalytic hydrogenation typically converts alkenes to alkanes by adding hydrogen across the double bond, resulting in a saturated compound without any double bonds. The reaction will yield a cyclopentane with two alkyl groups attached, replacing the double bond with single bonds.
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