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  2. Tris(pentafluorophenyl)borane - Wikipedia

    en.wikipedia.org/wiki/Tris(pentafluorophenyl)borane

    Tris(pentafluorophenyl)borane, sometimes referred to as "BCF", is the chemical compound (C 6 F 5) 3 B.It is a white, volatile solid. The molecule consists of three pentafluorophenyl groups attached in a "paddle-wheel" manner to a central boron atom; the BC 3 core is planar.

  3. Cycloisomerization - Wikipedia

    en.wikipedia.org/wiki/Cycloisomerization

    Cycloisomerization is any isomerization in which the cyclic isomer of the substrate is produced in the reaction coordinate.The greatest advantage of cycloisomerization reactions is its atom economical nature, by design nothing is wasted, as every atom in the starting material is present in the product.

  4. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    In chemistry, isomerization or isomerisation is the process in which a molecule, polyatomic ion or molecular fragment is transformed into an isomer with a different chemical structure. [1] Enolization is an example of isomerization, as is tautomerization .

  5. Bromopentafluorobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromopentafluorobenzene

    Bromopentafluorobenzene is an organofluorine compound with the formula C 6 F 5 Br. It is a colorless liquid that is used to prepare pentafluophenyl compounds. These syntheses typically proceed via the intermediacy of C 6 F 5 Li or the Grignard reagent. [1]

  6. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    In the third step, an isomerization step protonates the nitrogen atom leading to the amide. The Beckmann rearrangement mechanism The same computation with a hydroxonium ion and 6 molecules of water has the same result, but when the migrating substituent is a phenyl group, the mechanism favors the formation of an intermediate three-membered π ...

  7. Isomerase - Wikipedia

    en.wikipedia.org/wiki/Isomerase

    The isomerization energy, for example, for converting from a stable cis isomer to the less stable trans isomer is greater than for the reverse reaction, explaining why in the absence of isomerases or an outside energy source such as ultraviolet radiation a given cis isomer tends to be present in greater amounts than the trans isomer.

  8. Alkyne zipper reaction - Wikipedia

    en.wikipedia.org/wiki/Alkyne_zipper_reaction

    The alkyne zipper reaction is an organic reaction that involves isomerization of a non terminal alkyne into a terminal alkyne. This reaction was first reported by Alexey Favorsky in 1887 (J. Russ. Phys.-Chem. Soc., 19, 414 (1887)).

  9. Penex - Wikipedia

    en.wikipedia.org/wiki/Penex

    In the petroleum industry, much research has been done on the upgrading of light hydrocarbons.The realisation that normal pentane is one of the most important remaining components of naphtha that can be easily upgraded prompted Phillips Petroleum to investigate the various processes for converting normal (linear) pentane into (branched) isopentane.

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    b c6f5 3 isomerization worksheet answers page 150 2020 philippines pdf