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  2. C3-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C3-Benzenes

    The C 3-benzenes are a class of organic aromatic compounds which contain a benzene ring and three other carbon atoms. For the hydrocarbons with no further unsaturation, there are four isomers. The chemical formula for all the saturated isomers is C 9 H 12.

  3. File:Benzene bromination mechanism.svg - Wikipedia

    en.wikipedia.org/wiki/File:Benzene_bromination...

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  4. Flammability diagram - Wikipedia

    en.wikipedia.org/wiki/Flammability_diagram

    Flammability diagram for methane. Flammability diagrams show the control of flammability in mixtures of fuel, oxygen and an inert gas, typically nitrogen.Mixtures of the three gasses are usually depicted in a triangular diagram, known as a ternary plot.

  5. Benzene (data page) - Wikipedia

    en.wikipedia.org/wiki/Benzene_(data_page)

    *** Benzene is a carcinogen (cancer-causing agent). *** Very flammable. The pure material, and any solutions containing it, constitute a fire risk. Safe handling: Benzene should NOT be used at all unless no safer alternatives are available. If benzene must be used in an experiment, it should be handled at all stages in a fume cupboard.

  6. Mesitylene - Wikipedia

    en.wikipedia.org/wiki/Mesitylene

    Mesitylene or 1,3,5-trimethylbenzene is a derivative of benzene with three methyl substituents positioned symmetrically around the ring. The other two isomeric trimethylbenzenes are 1,2,4-trimethylbenzene (pseudocumene) and 1,2,3-trimethylbenzene (hemimellitene).

  7. m-Phenylenediamine - Wikipedia

    en.wikipedia.org/wiki/M-Phenylenediamine

    m-Phenylenediamine, also called 1,3-diaminobenzene, is an organic compound with the formula C 6 H 4 (NH 2) 2.It is an isomer of o-phenylenediamine and p-phenylenediamine.This aromatic diamine is a colourless solid that appears as needles, but turns red or purple on exposure to air due to formation of oxidation products. [3]

  8. Tetramethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Tetramethylbenzene

    The tetramethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with four methyl groups (–CH 3) as a substituent. [1] Through their different arrangement, they form three structural isomers with the molecular formula C 10 H 14. They also belong to the group of C 4-benzenes.

  9. Aromatization - Wikipedia

    en.wikipedia.org/wiki/Aromatization

    Aromatization is a chemical reaction in which an aromatic system is formed from a single nonaromatic precursor. Typically aromatization is achieved by dehydrogenation of existing cyclic compounds, illustrated by the conversion of cyclohexane into benzene.