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  2. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    The melting points of the alkanes follow a similar trend to boiling points for the same reason as outlined above. That is, (all other things being equal) the larger the molecule the higher the melting point. There is one significant difference between boiling points and melting points. Solids have a more rigid and fixed structure than liquids.

  3. 2,2-Dimethylbutane - Wikipedia

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

    2,2-Dimethylbutane, trivially known as neohexane at William Odling's 1876 suggestion, [4] is an organic compound with formula C 6 H 14 or (H 3 C-) 3-C-CH 2-CH 3. It is therefore an alkane , indeed the most compact and branched of the hexane isomers — the only one with a quaternary carbon and a butane (C 4 ) backbone.

  4. Tridecane - Wikipedia

    en.wikipedia.org/wiki/Tridecane

    Melting point: −6 to −4 °C; 21 to 25 °F; 267 to 269 K Boiling point: 232 to 236 °C; 449 to 457 °F; 505 to 509 K log P: ... Related alkanes. Dodecane;

  5. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    4.172 055 713 266 37 × 10 44: C 97 H 196: n-heptanonacontane 98 7.856 847 598 530 88 × 10 38: 1.336 772 071 150 80 × 10 45: C 98 H 198: n-octanonacontane 99 2.156 596 319 845 08 × 10 39: 4.284 272 900 597 84 × 10 45: C 99 H 200: n-nonanonacontane 100 5.921 072 038 125 81 × 10 39: 1.373 431 909 183 29 × 10 47: C 100 H 202: n-hectane 101 1 ...

  6. 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 ...

  7. Higher alkane - Wikipedia

    en.wikipedia.org/wiki/Higher_alkane

    Higher alkanes are naturally present in crude oil and can be obtained via fractional distillation.Saturated fatty acids decarboxylate to higher alkanes. Long olefins can be hydrogenated to yield higher alkanes. n-alkanes can be isolated via the formation of urea clathrates.They can also be synthesized through Kolbe electrolysis or other coupling reactions like the Wurtz reaction.

  8. Octadecane - Wikipedia

    en.wikipedia.org/wiki/Octadecane

    This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it.

  9. Decane - Wikipedia

    en.wikipedia.org/wiki/Decane

    Decane is an alkane hydrocarbon with the chemical formula C 10 H 22.Although 75 structural isomers are possible for decane, the term usually refers to the normal-decane ("n-decane"), with the formula CH 3 (CH 2) 8 CH 3.