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  2. 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 ...

  3. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    IUPAC name: Common name: Structural formula heptanoic acid: enanthic acid oenanthic acid n-Heptylic acid n-Heptoic acid: CH 3 (CH 2) 5 COOH heptanedioic acid: pimelic acid: HOOC(CH 2) 5 COOH cyclohexanecarboxylic acid: C 6 H 11 COOH: benzenecarboxylic acid: benzoic acid carboxybenzene dracylic acid: C 6 H 5 COOH: 2-hydroxybenzoic acid ...

  4. Ethane - Wikipedia

    en.wikipedia.org/wiki/Ethane

    Ethane (US: / ˈ ɛ θ eɪ n / ETH-ayn, UK: / ˈ iː θ eɪ n / EE-thayn) is a naturally occurring organic chemical compound with chemical formula C 2 H 6.At standard temperature and pressure, ethane is a colorless, odorless gas.

  5. Methyl radical - Wikipedia

    en.wikipedia.org/wiki/Methyl_radical

    Methyl radical is an organic compound with the chemical formula CH • 3 (also written as [CH 3] •). It is a metastable colourless gas, which is mainly produced in situ as a precursor to other hydrocarbons in the petroleum cracking industry. It can act as either a strong oxidant or a strong reductant, and is quite corrosive to metals.

  6. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    Molecular Formula Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl hydride; methylethyl methane 5 3 3 C 5 H 12: n-pentane: amyl hydride; Skellysolve A 6 5 5 C 6 H ...

  7. Acyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acyl_chloride

    If the structure of the acid and the acid chloride are different, the product is a mixed anhydride. First, the carboxylic acid attacks the acid chloride ( 1 ) to give tetrahedral intermediate 2 . The tetrahedral intermediate collapses, ejecting chloride ion as the leaving group and forming oxonium species 3 .

  8. Alcohol (chemistry) - Wikipedia

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

    In naming simple alcohols, the name of the alkane chain loses the terminal e and adds the suffix -ol, e.g., as in "ethanol" from the alkane chain name "ethane". [19] When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3.

  9. tert-Butyllithium - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyllithium

    tert-Butyllithium is a chemical compound with the formula (CH 3) 3 CLi. As an organolithium compound, it has applications in organic synthesis since it is a strong base, capable of deprotonating many carbon molecules, including benzene.

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