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  2. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Most aliphatic compounds are flammable, allowing the use of hydrocarbons as fuel, such as methane in natural gas for stoves or heating; butane in torches and lighters; various aliphatic (as well as aromatic) hydrocarbons in liquid transportation fuels like petrol/gasoline, diesel, and jet fuel; and other uses such as ethyne (acetylene) in welding.

  3. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one nitrogen atom. Hydrocarbons without an aromatic ring are called aliphatic. Approximately half of compounds known ...

  4. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon. [1]: 620 Hydrocarbons are examples of group 14 hydrides. Hydrocarbons are generally colourless and hydrophobic; their odor is usually faint, and may be similar to that of gasoline or lighter fluid.

  5. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    As of alkanes, they first dehydrogenate to olefins, then form rings at the place of the double bond, becoming cycloalkanes, and finally gradually lose hydrogen to become aromatic hydrocarbons. [ 4 ] For cyclohexane, cyclohexene, and cyclohexadiene, dehydrogenation is the conceptually simplest pathway for aromatization.

  6. Aromaticity - Wikipedia

    en.wikipedia.org/wiki/Aromaticity

    Two different resonance forms of benzene (top) combine to produce an average structure (bottom). In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected by the stabilization of conjugation alone.

  7. Organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Organic_chemistry

    Aromatic hydrocarbons contain conjugated double bonds. This means that every carbon atom in the ring is sp2 hybridized, allowing for added stability. The most important example is benzene, the structure of which was formulated by Kekulé who first proposed the delocalization or resonance principle for explaining its structure. For "conventional ...

  8. Cyclic compound - Wikipedia

    en.wikipedia.org/wiki/Cyclic_compound

    Cyclic compounds may or may not exhibit aromaticity; benzene is an example of an aromatic cyclic compound, while cyclohexane is non-aromatic. In organic chemistry, the term aromaticity is used to describe a cyclic (ring-shaped), planar (flat) molecule that exhibits unusual stability as compared to other geometric or connective arrangements of ...

  9. Wax - Wikipedia

    en.wikipedia.org/wiki/Wax

    Paraffin waxes are mixtures of saturated n- and iso- alkanes, naphthenes, and alkyl- and naphthene-substituted aromatic compounds. A typical alkane paraffin wax chemical composition comprises hydrocarbons with the general formula C n H 2n+2, such as hentriacontane, C 31 H 64. The degree of branching has an important influence on the properties.