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lecture10
lecture10

... Here E is the voltage (actually, it is the zero current potential -- the maximum voltage that could be produced by the system with not current flowing). The proportionality constant has two parts. Part (F, the Faraday constant) takes into account the fact that Gibbs free energy is on a per mole basi ...
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SG5 Chemical Reactions and Quantities

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Chemistry exam review
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... a. It is an exothermic reaction with an energy change of 160kJ. b. It is an exothermic reaction with an energy change of 80kJ. c. It is an endothermic reaction with an energy change of 160kJ. d. It is an endothermic reaction with an energy change of 80kJ. 4. What type of reaction is represented by t ...
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Chemistry exam review

Final Exam Review
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... a. It is an exothermic reaction with an energy change of 160kJ. b. It is an exothermic reaction with an energy change of 80kJ. c. It is an endothermic reaction with an energy change of 160kJ. d. It is an endothermic reaction with an energy change of 80kJ. 4. What type of reaction is represented by t ...
Energy and Chemical Reactions
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... i) Adsorption of reactant molecules from the gas phase onto the surface. ii) Dissociation of molecules on the surface. iii) Reaction between adsorbed molecules. iv) Desorption of the reaction product(s) to the gas phase. The assumptions underlying the Langmuir-Hinshelwood mechanism are: 1. The solid ...
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... calculator, and your University ID Card. If you have notes with you, place them in a sealed backpack and place the backpack OUT OF SIGHT or place the notes directly on the table at the front of the room. Fill in the front page of the Scantron answer sheet with your test form number (listed above), l ...
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... Rate1 = 2.6 x 10-6 = k [0.018]x [0.036]y Rate2 = 3.9 x 10-6 = k [0.027]x [0.036]y Rate3 = 7.8 x 10-6 = k [0.036]x [0.054]y Rate4 = 1.4 x 10-5 = k [0.050]x [0.072]y ...
The d-block elements are commonly known as transition
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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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