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  2. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    CH 3 (CH 2) 10 COOH benzene-1,2,3,4,5,6-hexacarboxylic acid: mellitic acid graphitic acid benzenehexacarboxylic acid: C 6 (COOH) 6: C13. IUPAC name: Common name ...

  3. 3-Hydroxybutanal - Wikipedia

    en.wikipedia.org/wiki/3-Hydroxybutanal

    CH 3 CH(OH)CH 2 CHO → CH 3 CH=CHCHO + H 2 O. Hydrogenation of 3-hydroxybutanal gives 1,3-butanediol: CH 3 CH(OH)CH 2 CHO + H 2 → CH 3 CH(OH)CH 2 CH 2 OH. This diol is a precursor to 1,3-butadiene, precursor to diverse polymers. Polymerization of 3-hydroxybutanal is also spontaneous, but can be stopped with the addition of water.

  4. 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 ...

  5. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    Propionaldehyde or propanal is the organic compound with the formula CH 3 CH 2 CHO. It is the 3-carbon aldehyde. It is a colourless, flammable liquid with a pungent and fruity odour. It is produced on a large scale industrially.

  6. (Mesitylene)molybdenum tricarbonyl - Wikipedia

    en.wikipedia.org/wiki/(Mesitylene)molybdenum_tri...

    (Mesitylene)molybdenum tricarbonyl arises from the reaction of molybdenum hexacarbonyl with hot mesitylene: [1]. Mo(CO) 6 + (CH 3) 3 C 6 H 3 → Mo(CO) 3 [(CH 3) 3 C 6 H 3] + 3 CO It can also be synthesized, with good yields by displacement of pyridine ligands of the trispyridine complex Mo(CO) 3 (pyridine) 3 in the presence of Lewis acids.

  7. Methenium - Wikipedia

    en.wikipedia.org/wiki/Methenium

    3 CN to form the ion (CH 3) 2 CN +. [5] Upon capture of a low-energy electron (less than 1 eV), it will spontaneously dissociate. [6] It is seldom encountered as an intermediate in the condensed phase. It is proposed as a reactive intermediate that forms upon protonation or hydride abstraction of methane with FSO 3 H-SbF 5. The methenium ion is ...

  8. Dimethylmercury - Wikipedia

    en.wikipedia.org/wiki/Dimethylmercury

    Dimethylmercury is an extremely toxic organomercury compound with the formula (CH 3) 2 Hg. A volatile, flammable, dense and colorless liquid, dimethylmercury is one of the strongest known neurotoxins. Less than 0.1 mL is capable of inducing severe mercury poisoning resulting in death. [2]

  9. 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).