When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals. Due to the cyclic continuous pi bonds between the carbon atoms, benzene is classed as an aromatic hydrocarbon. Benzene is a colorless and highly flammable liquid with a sweet smell, and is partially responsible for the aroma of gasoline.

  3. Trouton's rule - Wikipedia

    en.wikipedia.org/wiki/Trouton's_rule

    [2] [3] It is valid for many liquids; for instance, the entropy of vaporization of toluene is 87.30 J/(K·mol), that of benzene is 89.45 J/(K·mol), and that of chloroform is 87.92 J/(K·mol). Because of its convenience, the rule is used to estimate the enthalpy of vaporization of liquids whose boiling points are known.

  4. BTX (chemistry) - Wikipedia

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

    In the petroleum refining and petrochemical industries, the initialism BTX refers to mixtures of benzene, toluene, and the three xylene isomers, all of which are aromatic hydrocarbons. The xylene isomers are distinguished by the designations ortho – (or o –), meta – (or m –), and para – (or p –) as indicated in the adjacent diagram.

  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. 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 .

  7. Aromatic compound - Wikipedia

    en.wikipedia.org/wiki/Aromatic_compound

    Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] 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 ...

  8. Buchner ring expansion - Wikipedia

    en.wikipedia.org/wiki/Buchner_ring_expansion

    The Buchner ring expansion reaction was first used in 1885 by Eduard Buchner and Theodor Curtius [1] [2] who prepared a carbene from ethyl diazoacetate for addition to benzene using both thermal and photochemical pathways in the synthesis of cycloheptatriene derivatives. The resulting product was a mixture of four isomeric carboxylic acids ...

  9. Divinylbenzene - Wikipedia

    en.wikipedia.org/wiki/Divinylbenzene

    Divinylbenzene (DVB) is an organic compound with the chemical formula C 6 H 4 (CH=CH 2) 2 and structure H 2 C=CH−C 6 H 4 −HC=CH 2 (a benzene ring with two vinyl groups as substituents).It is related to styrene (vinylbenzene, C 6 H 5 −CH=CH 2) by the addition of a second vinyl group. [2]