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  2. List of isomers of decane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_decane

    This page was last edited on 18 November 2024, at 00:50 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  3. List of isomers of dodecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_dodecane

    The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.

  4. List of isomers of tridecane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_tridecane

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  5. 2-Methylheptane - Wikipedia

    en.wikipedia.org/wiki/2-Methylheptane

    2-Methylheptane is a branched-chain alkane and an isomer of octane.It is an heptane molecule with a methyl group attached to its second atom. It is a flammable colorless liquid used as fuel.

  6. 3-Methylheptane - Wikipedia

    en.wikipedia.org/wiki/3-Methylheptane

    114.232 g·mol −1 Appearance Colourless liquid Odor: Odourless Density: 705 mg mL −1: Melting point: −122 to −120 °C; −188 to −184 °F; 151 to 153 K Boiling point: 118 to 120 °C; 244 to 248 °F; 391 to 393 K Vapor pressure: 5.0 kPa (at 37.7 °C)

  7. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    Triphenylmethane was first synthesized in 1872 by the German chemist August Kekulé and his Dutch student Antoine Paul Nicolas Franchimont (1844–1919) by heating diphenylmercury (Hg(C 6 H 5) 2, Quecksilberdiphenyl) with benzal chloride (C 6 H 5 CHCl 2, Benzylenchlorid).

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  9. IUPAC nomenclature of organic chemistry - Wikipedia

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

    The side chains are: an ethyl- at carbon 4, an ethyl- at carbon 8, and a butyl- at carbon 12. Note: the −O−CH 3 at carbon atom 15 is not a side chain, but it is a methoxy functional group. There are two ethyl- groups. They are combined to create, 4,8-diethyl. The side chains are grouped like this: 12-butyl-4,8-diethyl.