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  2. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    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. Reactivity series - Wikipedia

    en.wikipedia.org/wiki/Reactivity_series

    Standard electrode potentials offer a quantitative measure of the power of a reducing agent, rather than the qualitative considerations of other reactive series. However, they are only valid for standard conditions: in particular, they only apply to reactions in aqueous solution.

  4. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    Additionally, the reactivity of two series of ketones are in the orders Cl 3 CCOCH 3 > CH 3 COCH 3 > C 6 H 5 COCH 3 and cyclohexanone > cyclopentanone > cycloheptanone > cyclooctanone. [7] [8] These orders of reactivity are the same as those observed for reactions that are well established as proceeding through nucleophilic attack on a carbonyl ...

  5. Circe effect - Wikipedia

    en.wikipedia.org/wiki/Circe_effect

    A corollary of the effect is to explain the existence of one-way enzymes that are much more effective catalysts for one direction of reaction than the other. For example, the limiting rate in the forward direction of the reaction catalyzed by methionine adenosyltransferase is about 2 × 10 5 times higher than it is for the reverse reaction. [5]

  6. Single displacement reaction - Wikipedia

    en.wikipedia.org/wiki/Single_displacement_reaction

    A single-displacement reaction, also known as single replacement reaction or exchange reaction, is an archaic concept in chemistry.It describes the stoichiometry of some chemical reactions in which one element or ligand is replaced by atom or group.

  7. Reactivity–selectivity principle - Wikipedia

    en.wikipedia.org/wiki/Reactivity–selectivity...

    The sulfur radical was found to be more reactive (6*10 8 vs. 1*10 7 M −1.s −1) and less selective (selectivity ratio 76 vs 1200) than the carbon radical. In this case, the effect can be explained by extending the Bell–Evans–Polanyi principle with a factor δ {\displaystyle \delta \,} accounting for transfer of charge from the reactants ...

  8. Alpha effect - Wikipedia

    en.wikipedia.org/wiki/Alpha_effect

    Other driving forces including the tighter transition state [10] and higher polarizability of α-nucleophiles, involvement of intramolecular catalysis also plays a role. Another in silico study did find a correlation between the alpha effect and the so-called deformation energy, which is the electronic energy required to bring the two reactants ...

  9. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    In commercial applications, the alkylating agents are generally alkenes, some of the largest scale reactions practiced in industry.Such alkylations are of major industrial importance, e.g. for the production of ethylbenzene, the precursor to polystyrene, from benzene and ethylene and for the production of cumene from benzene and propene in cumene process: