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  2. 3-Ethylpentane - Wikipedia

    en.wikipedia.org/wiki/3-ethylpentane

    3-Ethylpentane (C 7 H 16) is a branched saturated hydrocarbon. It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol. [3]

  3. 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 ...

  4. 3-Methylpentane - Wikipedia

    en.wikipedia.org/wiki/3-Methylpentane

    3-Methylpentane is a branched alkane with the molecular formula C 6 H 14. It is a structural isomer of hexane composed of a methyl group bonded to the third carbon atom in a pentane chain. It is of similar structure to the isomeric 2-methylpentane , which has the methyl group located on the second carbon of the pentane chain.

  5. File:Skeletal formula of 3-ethylpentane.svg - Wikipedia

    en.wikipedia.org/wiki/File:Skeletal_formula_of_3...

    This file contains additional information, probably added from the digital camera or scanner used to create or digitize it. If the file has been modified from its original state, some details may not fully reflect the modified file.

  6. List of isomers of nonane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_nonane

    5 Pentane. Toggle Pentane subsection. 5.1 Tetramethyl. 5.2 Dimethyl+ethyl. 5.3 Diethyl. Toggle the table of contents. ... 3-Ethyl-3-methylhexane; 3-Ethyl-4 ...

  7. 3-Ethyl-3-pentanol - Wikipedia

    en.wikipedia.org/wiki/3-Ethyl-3-pentanol

    3-Ethyl-3-pentanol, also known as 3-ethylpentan-3-ol, is a tertiary alcohol with the molecular formula C 7 H 16 O. It reacts with chromic acid by first dehydrating to an olefin 3-ethyl-2-pentene, and then by converting the double bond to an epoxide. [2] Perfluorination affords perfluorotriethylcarbinol, a powerful uncoupling agent.

  8. Meredith R. Spangler - Pay Pals - The Huffington Post

    data.huffingtonpost.com/paypals/meredith-r-spangler

    From January 2008 to April 2009, if you bought shares in companies when Meredith R. Spangler joined the board, and sold them when she left, you would have a -83.0 percent return on your investment, compared to a -44.7 percent return from the S&P 500.

  9. List of isomers of decane - Wikipedia

    en.wikipedia.org/wiki/List_of_isomers_of_decane

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