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  2. Acetonitrile - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile

    Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries. Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, it absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower.

  3. Acetonitrile (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile_(data_page)

    1.344 at 20.0 °C [1] Abbe number? Dielectric constant, ... log 10 of Acetonitrile vapor pressure. Uses formula ...

  4. Tetrakis(acetonitrile)copper(I) tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(acetonitrile...

    Tetrakis(acetonitrile)copper(I) tetrafluoroborate can be prepared starting from nitrosyl tetrafluoroborate, which is obtained from dinitrogen tetroxide and tetrafluoroboric acid. The nitrosyl salt is then reacted with metallic copper in acetonitrile , initially producing a green-blue copper(II) complex.

  5. Aminoacetonitrile - Wikipedia

    en.wikipedia.org/wiki/Aminoacetonitrile

    Aminoacetonitrile is the organic compound with the formula H 2 N−CH 2 −C≡N.The compound is a colorless liquid. It is unstable at room temperature, owing to the incompatibility of the amine nucleophile and the nitrile electrophile.

  6. Transition metal nitrile complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_nitrile...

    Typical nitrile ligands are acetonitrile, propionitrile, and benzonitrile.The structures of [Ru(NH 3) 5 (NCPh)] n+ have been determined for the 2+ and 3+ oxidation states. Upon oxidation the Ru-NH 3 distances contract and the Ru-NCPh distances elongate, consistent with amines serving as pure-sigma donor ligands and nitriles functioning as pi-acceptors.

  7. Methyl acetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_acetate

    Methyl acetate is produced industrially via the carbonylation of methanol as a byproduct of the production of acetic acid. [6] Methyl acetate also arises by esterification of acetic acid with methanol in the presence of strong acids such as sulfuric acid; this production process is famous [according to whom?] because of Eastman Kodak's intensified process using a reactive distillation.

  8. 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]

  9. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone (>C=O).It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.