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  2. Hydrogen-donor solvent - Wikipedia

    en.wikipedia.org/wiki/Hydrogen-donor_solvent

    A hydrogen-donor solvent is hydrocarbon that transfers hydrogen to hydrogen-poor substrates, such as coal.The hydrogen-poor substrates could be a solute or suspension. The classic hydrogen-donor solvent (or just donor solvent) is tetrahydronaphthalene, [1] which converts to naphthalene by transfer of two equivalents of H 2 to the substrate.

  3. Transfer hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Transfer_hydrogenation

    It uses hydrogen donor compounds such as formic acid, isopropanol or dihydroanthracene, dehydrogenating them to CO 2, acetone, or anthracene respectively. [1] Often, the donor molecules also function as solvents for the reaction. A large scale application of transfer hydrogenation is coal liquefaction using "donor solvents" such as tetralin. [2 ...

  4. Hydrogen donor - Wikipedia

    en.wikipedia.org/?title=Hydrogen_donor&redirect=no

    This page was last edited on 9 June 2009, at 17:36 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply ...

  5. Primary nutritional groups - Wikipedia

    en.wikipedia.org/wiki/Primary_nutritional_groups

    Organotrophs use organic compounds as electron/hydrogen donors. Lithotrophs use inorganic compounds as electron/hydrogen donors.. The electrons or hydrogen atoms from reducing equivalents (electron donors) are needed by both phototrophs and chemotrophs in reduction-oxidation reactions that transfer energy in the anabolic processes of ATP synthesis (in heterotrophs) or biosynthesis (in autotrophs).

  6. Hydrogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrogenation

    Gaseous hydrogen is produced industrially from hydrocarbons by the process known as steam reforming. [2] For many applications, hydrogen is transferred from donor molecules such as formic acid, isopropanol, and dihydroanthracene. [3] These hydrogen donors undergo dehydrogenation to, respectively, carbon dioxide, acetone, and anthracene.

  7. Barton decarboxylation - Wikipedia

    en.wikipedia.org/wiki/Barton_decarboxylation

    The product is then heated in the presence of a radical initiator and a suitable hydrogen donor to afford the decarboxylated product. [1] [2] This is an example of a reductive decarboxylation. Using this reaction it is possible to remove carboxylic acid moieties from alkyl groups and replace them with other functional groups.

  8. Diethyl azodicarboxylate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_azodicarboxylate

    Similarly, reacting DEAD with ethanol and cyclohexanol abstracts hydrogen producing acetaldehyde and cyclohexanone. Those reactions also proceed without light, although at much lower yields. [ 9 ] Thus, in general DEAD is an aza- dienophile and dehydrogenating agent, converting alcohols to aldehydes , thiols to disulfides and hydrazo groups to ...

  9. Tetralin - Wikipedia

    en.wikipedia.org/wiki/Tetralin

    Tetralin is used as a hydrogen-donor solvent, for example in coal liquifaction.It functions as a source of H 2, which is transferred to the coal.The partially hydrogenated coal is more soluble.