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  2. Cyclohexa-1,3-diene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexa-1,3-diene

    Compared with its isomer cyclohexa-1,4-diene, cyclohexa-1,3-diene is about 1.6 kJ/mol more stable. [5] Cyclohexadiene and its derivatives form (diene)iron tricarbonyl complexes. Illustrative is [(C 6 H 8)Fe(CO) 3], an orange liquid. This complex reacts with hydride-abstracting reagents to give the cyclohexadienyl derivative [(C 6 H 7)Fe(CO) 3 ...

  3. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    A mixture of cis-decalin and CXB can simultaneously match optical index and density of PMMA. [1] Due to the moderate dielectric constant of CXB (ε = 7.9 [2]), PMMA acquires charges that can be screened by the addition of salt (e.g. tetrabutyl ammonium bromide), leading to a very good approximation of colloidal hard sphere. [3]

  4. Cyclohexa-1,4-diene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexa-1,4-diene

    1,4-Cyclohexadiene is an organic compound with the formula C 6 H 8. It is a colourless, flammable liquid that is of academic interest as a prototype of a large class of related compounds called terpenoids, an example being γ-terpinene. An isomer of this compound is 1,3-cyclohexadiene.

  5. Cyclohexadiene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexadiene

    Cyclohexadiene may refer to: Cyclohexa-1,3-diene, Cyclohexa-1,4-diene, See also. Benzene or its theoretical isomer 1,3,5-Cyclohexatriene; Cyclohexene

  6. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    1,3-Cyclohexadiene. 1,4-Cyclohexadiene. 1,5-Cyclooctadiene. cis-cyclooctene. trans-cyclooctene. Nomenclature. Cycloalkenes follow a similar nomenclature system to ...

  7. Cyclohexene - Wikipedia

    en.wikipedia.org/wiki/Cyclohexene

    Benzene is converted to cyclohexylbenzene by acid-catalyzed alkylation with cyclohexene. [6] Cyclohexylbenzene is a precursor to both phenol and cyclohexanone. [7]Hydration of cyclohexene gives cyclohexanol, which can be dehydrogenated to give cyclohexanone, a precursor to caprolactam.

  8. Birch reduction - Wikipedia

    en.wikipedia.org/wiki/Birch_reduction

    The Birch reduction is an organic reaction that is used to convert arenes to 1,4-cyclohexadienes.The reaction is named after the Australian chemist Arthur Birch and involves the organic reduction of aromatic rings in an amine solvent (traditionally liquid ammonia) with an alkali metal (traditionally sodium) and a proton source (traditionally an alcohol).

  9. Bronidox - Wikipedia

    en.wikipedia.org/wiki/Bronidox

    Bronidox, or 5-bromo-5-nitro-1,3-dioxane, is an antimicrobial chemical compound. Bronidox causes inhibition of enzyme activity in bacteria. [3]