When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    On a carbon skeleton, sp 2-hybridized carbons or positions are often called vinylic. Allyls , acrylates and styrenics contain vinyl groups. (A styrenic crosslinker with two vinyl groups is called divinyl benzene .)

  3. Vinyl iodide functional group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_iodide_functional_group

    In S N 1 case, dissociation is difficult because of the strengthened C-I bond and loss of the iodide will generate an unstable carbocation(see figure 1c) [2] Figure 1. In cross-coupling reactions, typically vinyl iodides react faster and under more mild conditions than vinyl chloride and vinyl bromide. The order of reactivity is based on the ...

  4. Vinylogy - Wikipedia

    en.wikipedia.org/wiki/Vinylogy

    Delocalization of negative charge in a generic carboxylate anion, derived from an organic carboxylic acid (cf. acetic acid), and the corresponding vinylogous carboxylate anion (the "vinylog/vinylogue" of the carboxylate anion), where a vinyl group now separates the charged oxygen from the carbonyl (C=O) group.

  5. Vinyl cation - Wikipedia

    en.wikipedia.org/wiki/Vinyl_cation

    The vinyl cation is a carbocation with the positive charge on an alkene carbon. Its empirical formula of the parent ion is C 2 H + 3.Vinyl cation are invoked as reactive intermediates in solvolysis of vinyl halides, [1] [2] as well as electrophilic addition to alkynes and allenes.

  6. Photo-oxidation of polymers - Wikipedia

    en.wikipedia.org/wiki/Photo-oxidation_of_polymers

    Charge-transfer complexes of oxygen and polystyrene phenyl groups absorb light to form singlet oxygen, which acts as a radical initiator. [23] Carbonyl impurities in the polymer (c.f. acetophenone) also absorb light in the near ultraviolet range (300 to 400 nm), forming excited ketones able to abstract hydrogen atoms directly from the polymer. [24]

  7. Vinylation - Wikipedia

    en.wikipedia.org/wiki/Vinylation

    In organic chemistry, vinylation is the process of attaching a vinyl group (CH 2 =CH−) to a substrate.Many organic compounds contain vinyl groups, so the process has attracted significant interest, especially since the reaction scope includes substituted vinyl groups.

  8. Acrylic acid - Wikipedia

    en.wikipedia.org/wiki/Acrylic_acid

    Acrylic acid (IUPAC: prop-2-enoic acid) is an organic compound with the formula CH 2 =CHCOOH. It is the simplest unsaturated carboxylic acid, consisting of a vinyl group connected directly to a carboxylic acid terminus.

  9. α,β-Unsaturated carbonyl compound - Wikipedia

    en.wikipedia.org/wiki/Α,β-Unsaturated_carbonyl...

    α,β-Unsaturated carbonyl compounds featuring a carbonyl conjugated to an alkene that is terminal, or vinylic, contain the acryloyl group (H 2 C=CH−C(=O)−); it is the acyl group derived from acrylic acid. The preferred IUPAC name for the group is prop-2-enoyl, and it is also known as acrylyl or simply (and incorrectly) as acryl. Compounds ...

  1. Related searches why are vinylic carbs unstable in the morning light and clear background

    what is vinylic carbonvinyl cation reactive
    vinyl cation inductive effectvinylic carbon groups