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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 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. Nitrile reduction - Wikipedia

    en.wikipedia.org/wiki/Nitrile_reduction

    With diisobutylaluminium hydride. The mechanism for the reduction of a nitrile to an aldehyde with DIBAL-H. The hydride reagent Diisobutylaluminium hydride, or DIBAL-H, is commonly used to convert nitriles to the aldehyde. [14] Regarding the proposed mechanism, DIBAL forms a Lewis acid-base adduct with the nitrile by formation of an N-Al bond.

  5. 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 ...

  6. Nitrile - Wikipedia

    en.wikipedia.org/wiki/Nitrile

    The structure of a nitrile: the functional group is highlighted blue. In organic chemistry, a nitrile is any organic compound that has a −C≡N functional group.The name of the compound is composed of a base, which includes the carbon of the −C≡N, suffixed with "nitrile", so for example CH 3 CH 2 C≡N is called "propionitrile" (or propanenitrile). [1]

  7. Reductions with hydrosilanes - Wikipedia

    en.wikipedia.org/wiki/Reductions_with_hydrosilanes

    Reductions with hydrosilanes are methods used for hydrogenation and hydrogenolysis of organic compounds. The approach is a subset of ionic hydrogenation. In this particular method, the substrate is treated with a hydrosilane and auxiliary reagent, often a strong acid, resulting in formal transfer of hydride from silicon to carbon. [1]

  8. Nitrilase - Wikipedia

    en.wikipedia.org/wiki/Nitrilase

    Nitrilase was first discovered in the early 1960s for its ability to catalyze the hydration of a nitrile to a carboxylic acid. [2] Although it was known at the time that nitrilase could operate with wide substrate specificity in producing the corresponding acid, later studies reported the first NHase (nitrile hydratase) activity exhibited by nitrilase.

  9. Properties of water - Wikipedia

    en.wikipedia.org/wiki/Properties_of_water

    Water is the chemical substance with chemical formula H 2 O; one molecule of water has two hydrogen atoms covalently bonded to a single oxygen atom. [26] Water is a tasteless, odorless liquid at ambient temperature and pressure. Liquid water has weak absorption bands at wavelengths of around 750 nm which cause it to appear to have a blue color. [4]