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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 ]

  3. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Expressing resonance when drawing Lewis structures may be done either by drawing each of the possible resonance forms and placing double-headed arrows between them or by using dashed lines to represent the partial bonds (although the latter is a good representation of the resonance hybrid which is not, formally speaking, a Lewis structure).

  4. Polyacrylonitrile - Wikipedia

    en.wikipedia.org/wiki/Polyacrylonitrile

    PAN is soluble in polar solvents, such as dimethylformamide, dimethylacetamide, ethylene and propylene carbonates, and in aqueous solutions of sodium thiocyanate, zinc chloride or nitric acid. [13] Solubility parameters: 26.09 MPa 1/2 (25 °C) are 25.6 to 31.5 J 1/2 cm −3/2. Dielectric constants: 5.5 (1 kHz, 25 °C), 4.2 (1 MHz, 25 °C).Can ...

  5. 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.

  6. Anionic addition polymerization - Wikipedia

    en.wikipedia.org/wiki/Anionic_addition...

    Synthesis of block copolymers is one of the most important applications of living polymerization as it offers the best control over structure. The nucleophilicity of the resulting carbanion will govern the order of monomer addition, as the monomer forming the less nucleophilic propagating species may inhibit the addition of the more ...

  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. 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]

  9. Propylene - Wikipedia

    en.wikipedia.org/wiki/Propylene

    Propylene is also used to produce isopropyl alcohol (propan-2-ol), acrylonitrile, propylene oxide, and epichlorohydrin. [18] The industrial production of acrylic acid involves the catalytic partial oxidation of propylene. [19] Propylene is an intermediate in the oxidation to acrylic acid.