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  2. Hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrogenation

    Hydrogenation is a chemical reaction between molecular hydrogen (H 2) 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 ...

  3. Fat hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Fat_hydrogenation

    Fat hydrogenation is the process of combining unsaturated fat with hydrogen in order to partially or completely convert it into saturated fat. Typically this hydrogenation is done with liquid vegetable oils resulting in solid or semi-solid fats .

  4. Squalane - Wikipedia

    en.wikipedia.org/wiki/Squalane

    Squalane is the organic compound with the formula ((CH 3) 2 CH(CH 2) 3 CH(CH 3)(CH 2) 3 (CH 2) 3 CH(CH 3)(CH 2) 2) 2.A colorless hydrocarbon, it is the hydrogenated derivative of squalene, although commercial samples are derived from nature. [3]

  5. Liquid organic hydrogen carrier - Wikipedia

    en.wikipedia.org/wiki/Liquid_organic_hydrogen...

    Liquid organic hydrogen carriers (LOHC) are organic compounds that can absorb and release hydrogen through chemical reactions. LOHCs can therefore be used as storage media for hydrogen. In principle, every unsaturated compound (organic molecules with C-C double or triple bonds) can take up hydrogen during hydrogenation.

  6. Hydrogen compounds - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_compounds

    By some definitions, "organic" compounds are only required to contain carbon. However, most of them also contain hydrogen, and because it is the carbon-hydrogen bond that gives this class of compounds most of its particular chemical characteristics, carbon-hydrogen bonds are required in some definitions of the word "organic" in chemistry. [12]

  7. Lindlar catalyst - Wikipedia

    en.wikipedia.org/wiki/Lindlar_catalyst

    Alkyne hydrogenation is stereospecific, occurring via syn addition to give the cis-alkene. [4] For example the hydrogenation of acetylenedicarboxylic acid using Lindlar catalyst gives maleic acid rather than fumaric acid. An example of commercial use is the organic synthesis of vitamin A which involves an alkyne reduction with the Lindlar catalyst.

  8. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    A saturated compound is a chemical compound (or ion) that resists addition reactions, such as hydrogenation, oxidative addition, and binding of a Lewis base. The term is used in many contexts and for many classes of chemical compounds. Overall, saturated compounds are less reactive than unsaturated compounds.

  9. Hydrogen auto-transfer - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_auto-transfer

    Hydrogen auto-transfer, also known as borrowing hydrogen, is the activation of a chemical reaction by temporary transfer of two hydrogen atoms from the reactant to a catalyst and return of those hydrogen atoms back to a reaction intermediate to form the final product.