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  2. Category:Alkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkanes

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  3. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    Alkanes have the general chemical formula C n H 2n+2. The alkanes range in complexity from the simplest case of methane (CH 4), where n = 1 (sometimes called the parent molecule), to arbitrarily large and complex molecules, like pentacontane (C 50 H 102) or 6-ethyl-2-methyl-5-(1-methylethyl) octane, an isomer of tetradecane (C 14 H 30).

  4. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    The formula for acyclic saturated hydrocarbons (i.e., alkanes) is C n H 2n+2. [1]: 623 The most general form of saturated hydrocarbons, (whether linear or branched species, and whether with or without one or more rings) is C n H 2n+2(1-r), where r is the number of rings. Those with exactly one ring are the cycloalkanes.

  5. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    2 994 664 179 967 370 611: 3.486 951 955 119 47 × 10 21: C 51 H 104: n-henpentacontane: 52 8 031 081 780 535 296 591: 1.092 126 741 043 54 × 10 22: C 52 H 106: n-dopentacontane: 53 2.155 777 191 357 26 × 10 19: 3.423 721 299 907 32 × 10 22: C 53 H 108: n-tripentacontane: 54 5.791 918 087 314 84 × 10 19: 1.074 254 564 589 75 × 10 23: C 54 ...

  6. Cracking (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Cracking_(chemistry)

    In petrochemistry, petroleum geology and organic chemistry, cracking is the process whereby complex organic molecules such as kerogens or long-chain hydrocarbons are broken down into simpler molecules such as light hydrocarbons, by the breaking of carbon–carbon bonds in the precursors.

  7. Corey–House synthesis - Wikipedia

    en.wikipedia.org/wiki/Corey–House_synthesis

    The Corey–House synthesis (also called the Corey–Posner–Whitesides–House reaction and other permutations) is an organic reaction that involves the reaction of a lithium diorganylcuprate with an organic halide or pseudohalide (′) to form a new alkane, as well as an ill-defined organocopper species and lithium (pseudo)halide as byproducts.

  8. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    The naming of polycyclic alkanes such as bicyclic alkanes and spiro alkanes is more complex, with the base name indicating the number of carbons in the ring system, a prefix indicating the number of rings ( "bicyclo-" or "spiro-"), and a numeric prefix before that indicating the number of carbons in each part of each ring, exclusive of ...

  9. 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. [2] If the standard definition of the prefix "iso-" is strictly used then 2-methylheptane can be called "Isooctane".