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  2. Reductions with samarium(II) iodide - Wikipedia

    en.wikipedia.org/wiki/Reductions_with_samarium...

    Samarium (II) iodide is a one-electron reductant, and typically effects reduction through a series of electron transfer and proton transfer (from protic solvent) steps. [ 4 ][ 3 ] Reducible functional groups include: α-Functionalized carbonyl compounds. Ketones and aldehydes. Carboxylic acids (under strongly acidic or basic conditions) Organic ...

  3. Samarium(II) iodide - Wikipedia

    en.wikipedia.org/wiki/Samarium(II)_iodide

    Samarium (II) iodide. Samarium (II) iodide is an inorganic compound with the formula SmI 2. When employed as a solution for organic synthesis, it is known as Kagan 's reagent. SmI 2 is a green solid and forms a dark blue solution in THF. [1] It is a strong one-electron reducing agent that is used in organic synthesis.

  4. Hydrogen peroxide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_peroxide

    Hydrogen peroxide is a chemical compound with the formula H 2 O 2.In its pure form, it is a very pale blue [5] liquid that is slightly more viscous than water.It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution (3%–6% by weight) in water for consumer use and in higher concentrations for industrial use.

  5. Oxidizing agent - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_agent

    The international pictogram for oxidizing chemicals. Dangerous goods label for oxidizing agents. An oxidizing agent (also known as an oxidant, oxidizer, electron recipient, or electron acceptor) is a substance in a redox chemical reaction that gains or "accepts"/"receives" an electron from a reducing agent (called the reductant, reducer, or electron donor).

  6. Hydrogen peroxide–urea - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_peroxide–urea

    Upon dissolving in various solvents, the 1:1 complex dissociates back to urea and hydrogen peroxide. So just like hydrogen peroxide, the (erroneously) so-called adduct is an oxidizer but the release at room temperature in the presence of catalysts proceeds in a controlled manner. Thus the compound is suitable as a safe substitute for the ...

  7. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    Desulfonylation reactionsare chemical reactions leading to the removal of a sulfonylgroup from organic compounds. As the sulfonyl functional group is electron-withdrawing,[1]methods for cleaving the sulfur–carbon bonds of sulfones are typically reductive in nature. Olefination or replacement with hydrogenmay be accomplished using reductive ...

  8. Reduction of nitro compounds - Wikipedia

    en.wikipedia.org/wiki/Reduction_of_nitro_compounds

    The reduction of nitroaromatics is conducted on an industrial scale. [1] Many methods exist, such as: Catalytic hydrogenation using: Raney nickel [2] or palladium-on-carbon, [3] [4] [5] platinum(IV) oxide, or Urushibara nickel. [6] Iron in acidic media. [7] [8] [9] Sodium hydrosulfite [10] Sodium sulfide (or hydrogen sulfide and base ...

  9. Advanced oxidation process - Wikipedia

    en.wikipedia.org/wiki/Advanced_oxidation_process

    Advanced oxidation processes (AOPs), in a broad sense, are a set of chemical treatment procedures designed to remove organic (and sometimes inorganic) materials in water and wastewater by oxidation through reactions with hydroxyl radicals (·OH). [ 1 ] In real-world applications of wastewater treatment, however, this term usually refers more ...