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  2. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. [1] Alkanes have the general chemical formula C n H 2n+2.

  3. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    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 14: n-hexane: dipropyl; Gettysolve-B; hexyl hydride; Skellysolve B 7 9 11 C 7 H 16: n-heptane: dipropyl methane; Gettysolve-C; heptyl hydride; Skellysolve C 8 18 24 C 8 H 18: n-octane: dibutyl; octyl hydride 9 35 55 C ...

  4. Hexadecane - Wikipedia

    en.wikipedia.org/wiki/Hexadecane

    Hexadecane (also called cetane) is an alkane hydrocarbon with the chemical formula C 16 H 34. Hexadecane consists of a chain of 16 carbon atoms , with three hydrogen atoms bonded to the two end carbon atoms, and two hydrogens bonded to each of the 14 other carbon atoms.

  5. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    Unsaturated compounds generally carry out typical addition reactions that are not possible with saturated compounds such as alkanes. A saturated organic compound has only single bonds between carbon atoms. An important class of saturated compounds are the alkanes. Many saturated compounds have functional groups, e.g., alcohols.

  6. 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.

  7. Category:Alkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkanes

    Alkanes as substituents are called alkyl groups Subcategories. This category has the following 5 subcategories, out of 5 total. B. Butane (2 C, 11 P) E. Ethane (1 C ...

  8. Nitro compound - Wikipedia

    en.wikipedia.org/wiki/Nitro_compound

    Free radical nitration of alkanes. [4] The reaction produces fragments from the parent alkane, creating a diverse mixture of products; for instance, nitromethane , nitroethane , 1-nitropropane , and 2-nitropropane are produced by treating propane with nitric acid in the gas phase (e.g. 350–450 °C and 8–12 atm ).

  9. 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 ...