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  2. 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]

  3. 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.

  4. Nitrile rubber - Wikipedia

    en.wikipedia.org/wiki/Nitrile_rubber

    Nitrile rubber, also known as nitrile butadiene rubber, NBR, Buna-N, and acrylonitrile butadiene rubber, is a synthetic rubber derived from acrylonitrile (ACN) and butadiene. [1] Trade names include Perbunan, Nipol, Krynac and Europrene. This rubber is unusual in being resistant to oil, fuel, and other chemicals.

  5. Acetonitrile - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile

    Acetonitrile, often abbreviated MeCN (methyl cyanide), is the chemical compound with the formula CH 3 CN and structure H 3 C−C≡N.This colourless liquid is the simplest organic nitrile (hydrogen cyanide is a simpler nitrile, but the cyanide anion is not classed as organic).

  6. Pinner reaction - Wikipedia

    en.wikipedia.org/wiki/Pinner_reaction

    The determining factor is typically how electron-rich or poor the nitrile is. For example: an electron-poor nitrile is a good electrophile (readily susceptible to attack from alkoxides etc.) but a poor nucleophile would typically be easier to protonate than to participate in the reaction and hence would be expected to react more readily under ...

  7. Nitrile anion - Wikipedia

    en.wikipedia.org/wiki/Nitrile_anion

    After protection of the hydroxyl group with an acyl or silyl group, cyanohydrins can function essentially as masked acyl anions. Because ester protecting groups are base labile, mild bases must be employed with ester-protected cyanohydrins. α-(Dialkylamino)nitriles can also be used in this context.

  8. Acrylonitrile - Wikipedia

    en.wikipedia.org/wiki/Acrylonitrile

    Its molecular structure consists of a vinyl group (−CH=CH 2) linked to a nitrile (−C≡N). It is an important monomer for the manufacture of useful plastics such as polyacrylonitrile. It is reactive and toxic at low doses. [5] Acrylonitrile is one of the components of ABS plastic (acrylonitrile butadiene styrene). [6]

  9. Medical glove - Wikipedia

    en.wikipedia.org/wiki/Medical_glove

    Dentist wearing nitrile gloves Medical gloves are disposable gloves used during medical examinations and procedures to help prevent cross-contamination between caregivers and patients. [ 1 ] Medical gloves are made of different polymers including latex , nitrile rubber , polyvinyl chloride and neoprene ; they come unpowdered, or powdered with ...