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Lithium chloride ionic association in dilute aqueous solution: a
Lithium chloride ionic association in dilute aqueous solution: a

... rB Þ=rAB is the unit vector from ion A to ion B; ~ FA and ~ FB are the total forces acting on the two ions, respectively; hicond represents the conditional star tistical average corresponding to a interionic distance of r. Note that in the constrained molecular dynamics, not only the interionic dist ...
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... 34) In the titration of 20.0 mL of 0.200 M HOBr with 0.100 M NaOH, what is the pH after 20.0 mL of the NaOH solution is added? (Ka HOBr = 2.5 × 10-9) A) 8.60 B) 4.65 C) 5.74 D) 7.00 E) none of these ...
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... Since Sandhage et al. used hot Mg vapor to reduce diatom frustules to porous silicon replicas in 200716, various silicon nanostructures, including nanoporous film17, nanocrystals18, porous silicon19, and 1D nanostructures20–22 have been synthesized by the same magnesiothermic reduction reaction (MRR ...
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... anode (oxidation): 2H2O(l) →O2(g) + 4H+(aq) + 4e– (to electrode) The gas produced at the anode is oxygen, which does not burn, so this is also consistent with the observations reported in the problem statement. (b) In the concentrated aqueous NaCl solution, the cathode reaction produces a basic solu ...
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Transition state theory



Transition state theory (TST) explains the reaction rates of elementary chemical reactions. The theory assumes a special type of chemical equilibrium (quasi-equilibrium) between reactants and activated transition state complexes.TST is used primarily to understand qualitatively how chemical reactions take place. TST has been less successful in its original goal of calculating absolute reaction rate constants because the calculation of absolute reaction rates requires precise knowledge of potential energy surfaces, but it has been successful in calculating the standard enthalpy of activation (Δ‡Hɵ), the standard entropy of activation (Δ‡Sɵ), and the standard Gibbs energy of activation (Δ‡Gɵ) for a particular reaction if its rate constant has been experimentally determined. (The ‡ notation refers to the value of interest at the transition state.)This theory was developed simultaneously in 1935 by Henry Eyring, then at Princeton University, and by Meredith Gwynne Evans and Michael Polanyi of the University of Manchester. TST is also referred to as ""activated-complex theory,"" ""absolute-rate theory,"" and ""theory of absolute reaction rates.""Before the development of TST, the Arrhenius rate law was widely used to determine energies for the reaction barrier. The Arrhenius equation derives from empirical observations and ignores any mechanistic considerations, such as whether one or more reactive intermediates are involved in the conversion of a reactant to a product. Therefore, further development was necessary to understand the two parameters associated with this law, the pre-exponential factor (A) and the activation energy (Ea). TST, which led to the Eyring equation, successfully addresses these two issues; however, 46 years elapsed between the publication of the Arrhenius rate law, in 1889, and the Eyring equation derived from TST, in 1935. During that period, many scientists and researchers contributed significantly to the development of the theory.
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