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  2. Pentane - Wikipedia

    en.wikipedia.org/wiki/Pentane

    Pentane is an organic compound with the formula C 5 H 12 —that is, an alkane with five carbon atoms. The term may refer to any of three structural isomers, or to a mixture of them: in the IUPAC nomenclature, however, pentane means exclusively the n-pentane isomer, in which case pentanes refers to a mixture of them; the other two are called isopentane (methylbutane) and neopentane ...

  3. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    CH 2 =CHCO 2 H Propiolic acid: propynoic acid propargylic acid acetylene carboxylic acid CH≡CCO 2 H Lactic acid: 2-hydroxypropanoic acid milk acid CH 3 CHOHCO 2 H 3-Hydroxypropionic acid: 3-hydroxypropanoic acid hydracrylic acid CH 2 OHCH 2 CO 2 H Glyceric acid: 2,3-dihydroxypropanoic acid CH 2 OHCHOHCO 2 H Pyruvic acid: 2-oxopropanoic acid ...

  4. Isopentane - Wikipedia

    en.wikipedia.org/wiki/Isopentane

    2 (C 2 H 5). Isopentane is a volatile and flammable liquid. It is one of three structural isomers with the molecular formula C 5 H 12, the others being pentane (n-pentane) and neopentane (2,2-dimethylpropane). Isopentane is commonly used in conjunction with liquid nitrogen to achieve a liquid bath temperature of −160 °C.

  5. Catenation - Wikipedia

    en.wikipedia.org/wiki/Catenation

    Catenation ability is also influenced by a range of steric and electronic factors, including the electronegativity of the element in question, the molecular orbital n and the ability to form different kinds of covalent bonds. For carbon, the sigma overlap between adjacent atoms is sufficiently strong that perfectly stable chains can be formed.

  6. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The longest possible main alkane chain is used; therefore 3-ethyl-4-methylhexane instead of 2,3-diethylpentane, even though these describe equivalent structures. The di-, tri- etc. prefixes are ignored for the purpose of alphabetical ordering of side chains (e.g. 3-ethyl-2,4-dimethylpentane, not 2,4-dimethyl-3-ethylpentane).

  7. C7H16 - Wikipedia

    en.wikipedia.org/wiki/C7H16

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  8. 2,2-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dimethylpentane

    2,2-Dimethylpentane does not react with bromine, iodine, nitric acid or chlorosulfonic acid because there are no tertiary carbon atoms (a carbon atom with only one hydrogen attached). [ 10 ] Heating alkanes over an aluminium trichloride is used to reform to make different isomers. 2,2-Dimethylpentane does not participate in this process and so ...

  9. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    2,3-Dimethylpentane is notable for being one of the two simplest alkanes with optical (enantiomeric) isomerism. The optical center is the middle carbon of the pentane backbone, which is connected to one hydrogen atom, one methyl group, one ethyl group – C 2 H 5, and one isopropyl group – CH(CH 3) 2.