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B.Sc Chemistry - Calicut University
B.Sc Chemistry - Calicut University

Mole-Volume Conversion Assignment
Mole-Volume Conversion Assignment

Mole
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... The electrode potential is further termed as oxidation potential if oxidation takes place at the electrode with respect to standard hydrogen electrode and is called reduction potential. If in the half-cell, the metal rod is suspended in a solution of one molar concentration and the temperature is ke ...
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... restricted. This amounts to decrease in the entropy of the gas after adsorption, i.e., ∆S is negative. Adsorption is thus accompanied by decrease in enthalpy as well as decrease in entropy of the system. For a process to be spontaneous, the thermodynamic requirement is that, at constant temperature ...
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... 27. An average home in Colorado requires 20. GJ of heat per month. How many grams of natural gas (methane) must be burned to supply this energy? CH4(g) + 2O2(g)  CO2(g) + 2H2O(l) H°rxn= –890.4 kJ/mol A) 1.4  103 g D) 2.2  104 g B) 3.6  105 g E) 1.4  104 g C) 7.1  10–4 g Ans: B 28. According t ...
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... Step 1: Express the equilibrium concentrations of all species in terms of initial concentrations and a single unknown x, that represents the change in concentration. Let (−x) be the depletion in concentration (mol/L) of HF. From the stoichiometry of the reaction, it follows that the increase in conc ...
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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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