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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

    1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 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 ...

  4. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Alkane C 2 H 2: Acetylene: Alkyne C 2 H 4: Ethylene: Alkene C 2 H 6: Ethane: Alkane C 3 H 4: Propyne: Alkyne C 3 H 6: Propene: Alkene C 3 H 8: Propane: Alkane C 4 H 6: 1,2-Butadiene: Diene: C 4 H 6: 1-Butyne: Alkyne C 4 H 8: 1-Butene: Alkene C 4 H 10: Butane: Alkane C 6 H 10: Cyclohexene: Cycloalkene C 5 H 12: n-pentane: Alkane C 7 H 14 ...

  5. Category:Alkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkanes

    An alkane is an acyclic saturated hydrocarbon. ... Ethane (1 C, 2 P) I. Lists of isomers of alkanes (6 P) M. Methane (3 C, 52 P) P. Propane (4 C, 16 P) Pages in ...

  6. Tetracosane - Wikipedia

    en.wikipedia.org/wiki/Tetracosane

    Tetracosane, also called tetrakosane, is an alkane hydrocarbon with the structural formula H(CH 2) 24 H. As with other alkanes, its name is derived from Greek for the number of carbon atoms, 24, in the molecule. It has 14,490,245 constitutional isomers, [2] and 252,260,276 stereoisomers. [3]

  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. 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 ...

  9. Alkanolamine - Wikipedia

    en.wikipedia.org/wiki/Alkanolamine

    2-Aminoalcohols are an important class of organic compounds that are often generated by the reaction of amines with epoxides: C 2 H 4 O + R−NH 2 → RNHC 2 H 4 OH. Simple alkanolamines are used as solvents, synthetic intermediates, and high-boiling bases. [1] Hydrogenation or hydride reduction of amino acids gives the