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  2. Methylidyne radical - Wikipedia

    en.wikipedia.org/wiki/Methylidyne_radical

    HCCo 3 (CO) 9, a metal cluster complex with a methylidyne ligand.. As an odd-electron species, CH is a radical. The ground state is a doublet (X 2 Π).The first two excited states are a quartet (with three unpaired electrons) (a 4 Σ −) and a doublet (A 2 Δ).

  3. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    This is a free rotation only in the simplest cases like gaseous methyl chloride CH 3 Cl. In most molecules, the remainder R breaks the C ∞ symmetry of the R−C axis and creates a potential V(φ) that restricts the free motion of the three protons. For the model case of ethane CH 3 CH 3, this is discussed under the name ethane barrier. In ...

  4. Methine group - Wikipedia

    en.wikipedia.org/wiki/Methine_group

    Methine or methylylidene (IUPAC) In organic chemistry, a methine group or methine bridge is a trivalent functional group =CH−, derived formally from methane.It consists of a carbon atom bound by two single bonds and one double bond, where one of the single bonds is to a hydrogen.

  5. Methylene (compound) - Wikipedia

    en.wikipedia.org/wiki/Methylene_(compound)

    [CH 2] 2• (X̃ 3 B 1) + H 2 O → [CH 3] • + [HO] • [CH 2] (ã 1 A 1) + H 2 O → H 2 CO + H 2 or H 3 COH. The singlet state is also more stereospecific than the triplet. [10] Methylene spontaneously autopolymerises to form various excited oligomers, the simplest of which, is the excited form of the alkene ethylene. The excited oligomers ...

  6. Pyrazole - Wikipedia

    en.wikipedia.org/wiki/Pyrazole

    Pyrazole is a weak base, with pK b 11.5 (pK a of the conjugate acid 2.49 at 25 °C). [3] According to X-ray crystallography , the compound is planar. The two C-N distances are similar, both near 1.33 Å [ 4 ]

  7. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The conversion of ethanol to ethylene is a fundamental example: [3] [4] CH 3 CH 2 OH → H 2 C=CH 2 + H 2 O. The reaction is accelerated by acid catalysts such as sulfuric acid and certain zeolites. These reactions often proceed via carbocation intermediates as shown for the dehydration of cyclohexanol. [5] Some alcohols are prone to dehydration.

  8. AOL Mail - AOL Help

    help.aol.com/products/aol-webmail

    Get answers to your AOL Mail, login, Desktop Gold, AOL app, password and subscription questions. Find the support options to contact customer care by email, chat, or phone number.

  9. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    Organochlorine chemistry is concerned with the properties of organochlorine compounds, or organochlorides, organic compounds containing at least one covalently bonded atom of chlorine. The chloroalkane class (alkanes with one or more hydrogens substituted by chlorine) includes common examples. The wide structural variety and divergent chemical ...