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  2. 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 ]

  3. Ethylcyclohexane - Wikipedia

    en.wikipedia.org/wiki/Ethylcyclohexane

    The molecule consists of an ethyl group attached to a cyclohexane ring. It is a typical naphthene in petroleum. It can be produced by hydrogenation of ethylbenzene and by hydrodeoxygenation of lignin .

  4. BTX (chemistry) - Wikipedia

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

    Structural diagrams of the BTX hydrocarbons. 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.

  5. 1-Bromohexane - Wikipedia

    en.wikipedia.org/wiki/1-Bromohexane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] 1-Bromohexane undergoes reactions expected of simple alkyl bromides. It can form Grignard reagents. [3]

  6. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

  7. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    Bromoethane, also known as ethyl bromide, is a chemical compound of the haloalkanes group. It is abbreviated by chemists as EtBr (which is also used as an abbreviation for ethidium bromide ). This volatile compound has an ether-like odor.

  8. A value - Wikipedia

    en.wikipedia.org/wiki/A_value

    Possible equatorial conformations of ethyl cyclohexane. Due to the larger number of possible conformations of ethyl cyclohexane, the A value is reduced from what would be predicted based purely on enthalpic terms. Due to these favorable entropic conditions, the steric relevance of an ethyl group is similar to that of a methyl substituent.

  9. Benzyl bromide - Wikipedia

    en.wikipedia.org/wiki/Benzyl_bromide

    Benzyl bromide is used in organic synthesis for the introduction of the benzyl groups when the less expensive benzyl chloride is insufficiently reactive. [6] [7] Benzylations are often achieved in the presence of catalytic amounts of sodium iodide, which generates the more reactive benzyl iodide in situ. [3]