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hydrogenate$36444$ - vertaling naar grieks
CHEMICAL REACTION BETWEEN MOLECULAR HYDROGEN AND ANOTHER COMPOUND OR ELEMENT, USUALLY IN THE PRESENCE OF A CATALYST SUCH AS NICKEL, PALLADIUM OR PLATINUM
Hydrogenated; Catalytic addition of hydrogen; Hydrogenate; Hydrogenated Oils; Hydrogenated cooking oils; Biohydrogenation; Hydrogenated vegetable oils; Hydrogenated oils; Catalytic hydrogenation; Hydrogenated protein; Partially hydrogenated oil; Partially Hydrogenated Oils; Homogeneous hydrogenation catalysis; User:Kwedar1/sandbox; Wikipedia talk:Articles for creation/Rhodium Catalyzed Hydrogenation; Rhodium Catalyzed Hydrogenation; Rhodium catalyzed hydrogenation; Hydrogenator; Hydroretorting; Hydroretorting process; Rhodium-catalyzed hydrogenation; Hydrogenation energy
![The [[transition state]] of two transfer-hydrogenation reactions from ruthenium-hydride complexes onto carbonyls](https://commons.wikimedia.org/wiki/Special:FilePath/THintermed.png?width=200 "The [[transition state]] of two transfer-hydrogenation reactions from ruthenium-hydride complexes onto carbonyls")
![[[Dichlorotris(triphenylphosphine)ruthenium(II)]] is a precatalyst based on ruthenium.](https://commons.wikimedia.org/wiki/Special:FilePath/Dichlorotris(triphenylphosphine)ruthenium(II).png?width=200 "[[Dichlorotris(triphenylphosphine)ruthenium(II)]] is a precatalyst based on ruthenium.")
![[[Crabtree's catalyst]] is a highly active catalyst featuring iridium.](https://commons.wikimedia.org/wiki/Special:FilePath/Crabtree.svg?width=200 "[[Crabtree's catalyst]] is a highly active catalyst featuring iridium.")
![[[(S)-iPr-PHOX]] is a typical chelating phosphine ligand used in asymmetric hydrogenation.](https://commons.wikimedia.org/wiki/Special:FilePath/(S)-iPr-PHOX.svg?width=200 "[[(S)-iPr-PHOX]] is a typical chelating phosphine ligand used in asymmetric hydrogenation.")
![Partial hydrogenation of [[phenylacetylene]] using the [[Lindlar catalyst]].](https://commons.wikimedia.org/wiki/Special:FilePath/PhC2HH2.png?width=200 "Partial hydrogenation of [[phenylacetylene]] using the [[Lindlar catalyst]].")
![Hydrogenation of an imine using a [[Raney nickel]] catalyst, a popular heterogeneous catalyst.](https://commons.wikimedia.org/wiki/Special:FilePath/ImineH2.png?width=200 "Hydrogenation of an imine using a [[Raney nickel]] catalyst, a popular heterogeneous catalyst.")
![Partial hydrogenation of a [[resorcinol]] derivative using a Raney-Nickel catalyst.](https://commons.wikimedia.org/wiki/Special:FilePath/ResorcinolH2.png?width=200 "Partial hydrogenation of a [[resorcinol]] derivative using a Raney-Nickel catalyst.")
hydrogenate
v. υδρογονώ
Wikipedia
Hydrogenation
Hydrogenation is a chemical reaction between molecular hydrogen (H2) and another compound or element, usually in the presence of a catalyst such as nickel, palladium or platinum. The process is commonly employed to reduce or saturate organic compounds. Hydrogenation typically constitutes the addition of pairs of hydrogen atoms to a molecule, often an alkene. Catalysts are required for the reaction to be usable; non-catalytic hydrogenation takes place only at very high temperatures. Hydrogenation reduces double and triple bonds in hydrocarbons.
