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  2. Acrylonitrile - Wikipedia

    en.wikipedia.org/wiki/Acrylonitrile

    Acrylonitrile is an organic compound with the formula CH 2 CHCN and the structure H 2 C=CH−C≡N. It is a colorless, volatile liquid although commercial samples can be yellow due to impurities. It has a pungent odor of garlic or onions. [4] Its molecular structure consists of a vinyl group (−CH=CH 2) linked to a nitrile (−C≡N).

  3. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  4. Polyacrylonitrile - Wikipedia

    en.wikipedia.org/wiki/Polyacrylonitrile

    Acrylonitrile is commonly employed as a comonomer with styrene, e.g. acrylonitrile, styrene and acrylate plastics. Labelling of items of clothing with acrylic (see acrylic fiber) means the polymer consists of at least 85% acrylonitrile as the monomer. A typical comonomer is vinyl acetate, which can be solution-spun readily to obtain fibers that ...

  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). It is produced mainly as a byproduct of acrylonitrile manufacture.

  6. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    Chemical structure of the vinyl functional group. In organic chemistry , a vinyl group (abbr. Vi ; [ 1 ] IUPAC name : ethenyl group [ 2 ] ) is a functional group with the formula −CH=CH 2 . It is the ethylene (IUPAC name: ethene) molecule ( H 2 C=CH 2 ) with one fewer hydrogen atom.

  7. Propionitrile - Wikipedia

    en.wikipedia.org/wiki/Propionitrile

    The main industrial route to this nitrile is the hydrogenation of acrylonitrile. It is also prepared by the ammoxidation of propanol (propionaldehyde can also be used instead): [7] CH 3 CH 2 CH 2 OH + O 2 + NH 3 → CH 3 CH 2 C≡N + 3 H 2 O. Propionitrile is a byproduct of the electrodimerisation of acrylonitrile to adiponitrile.

  8. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  9. Cyanoethylation - Wikipedia

    en.wikipedia.org/wiki/Cyanoethylation

    The β-carbon atom that is furthest from the nitrile group is positively polarized and therefore binds the heteroatom on the nucleophile. Acrylonitrile is a Michael acceptor. [2] The reaction is normally catalyzed by a base. [3] Tris(cyanoethyl)phosphine is produced by the cyanoethylation of phosphine. [4]