Alkene Reduction

Alkene reduction is a chemical transformation that converts a carbon-carbon double bond into a single bond, typically by adding hydrogen across the alkene. In catalytic hydrogenation, molecular hydrogen interacts with a metal catalyst such as palladium, platinum, or nickel, enabling stepwise addition of hydrogen atoms to the double bond and often producing syn addition. This reaction changes molecular saturation and can influence stereochemistry, selectivity, and physical properties. It is widely used in organic synthesis, pharmaceutical and fine-chemical manufacturing, and the preparation of fuels, fats, and other reduced compounds.

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JoVE Core - Organic Chemistry
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Oxymercuration-Reduction of Alkenes

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2025

Oxymercuration–reduction of alkenes is one of the major reactions converting alkenes to alcohols. It involves the hydration of alkenes with mercuric acetate in a mixture of tetrahydrofuran and water, forming an organomercury adduct. This is followed by a demercuration step in which the adduct is reduced to an alcohol using sodium borohydride. In the mixture of water and tetrahydrofuran, tetrahydrofuran acts as a solvent dissolving the alkene and the aqueous mercuric acetate solution, while...

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JoVE Core - Organic Chemistry
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Reduction of Alkenes: Catalytic Hydrogenation

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2023

Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation. Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts. The hydrogenation process takes place on the surface of...

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JoVE Science Education - Chemistry

Ozonolysis of Alkenes

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2023

Source: Vy M. Dong and Zhiwei Chen, Department of Chemistry, University of California, Irvine, CA This experiment will demonstrate an example of an ozonolysis reaction to synthesize vanillin from isoeugenol (Figure 1). Ozonolysis of alkenes, an oxidation reaction between ozone and an alkene, is a common method to prepare aldehydes, ketones, and carboxylic acids. This experiment also demonstrates the use of an ozone generator and a low temperature (−78 °C) reaction. Figure 1. Diagram showing...

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JoVE Core - Organic Chemistry
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Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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2023

Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry. The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation

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2023

Introduction Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate. Thermodynamic Stability Catalytic hydrogenation reactions help evaluate the relative thermodynamic stability of hydrocarbons. For example, the heat of hydrogenation of acetylene is −176 kJ/mol, and that of ethylene is −137 kJ/mol. The higher exothermicity associated with...

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