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  2. 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).

  3. 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 ...

  4. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes. A Newman projection visualizes the conformation of a chemical bond from front to back, with the front atom represented by the intersection of three lines (a dot) and the back atom as a circle.

  5. Rotamers - Wikipedia

    en.wikipedia.org/wiki/Alkane_stereochemistry

    Naming alkanes per standards listed in the IUPAC Gold Book is done according to the Klyne–Prelog system for specifying angles (called either torsional or dihedral angles) between substituents around a single bond: [25] syn/anti peri/clinal. a torsion angle between 0° and ±90° is called syn (s) a torsion angle between ±90° and 180° is ...

  6. 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 ...

  7. Fluid catalytic cracking - Wikipedia

    en.wikipedia.org/wiki/Fluid_catalytic_cracking

    Figure 2 is a very simplified schematic diagram that exemplifies how the process breaks high boiling, straight-chain alkane (paraffin) hydrocarbons into smaller straight-chain alkanes as well as branched-chain alkanes, branched alkenes (olefins) and cycloalkanes (naphthenes).

  8. 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.

  9. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–carbon_bond

    Carbon is one of the few elements that can form long chains of its own atoms, a property called catenation.This coupled with the strength of the carbon–carbon bond gives rise to an enormous number of molecular forms, many of which are important structural elements of life, so carbon compounds have their own field of study: organic chemistry.