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Chemical kinetics, also known as reaction kinetics, is the branch of physical chemistry that is concerned with understanding the rates of chemical reactions. It is different from chemical thermodynamics , which deals with the direction in which a reaction occurs but in itself tells nothing about its rate.
Chemical kinetics is the part of physical chemistry that concerns how rates of chemical reactions are measured and predicted, and how reaction-rate data can be used to deduce probable reaction mechanisms. [2] The concepts of chemical kinetics are applied in many disciplines, such as chemical engineering, [3] [4] enzymology and environmental ...
where A and B are reactants C is a product a, b, and c are stoichiometric coefficients,. the reaction rate is often found to have the form: = [] [] Here is the reaction rate constant that depends on temperature, and [A] and [B] are the molar concentrations of substances A and B in moles per unit volume of solution, assuming the reaction is taking place throughout the volume of the ...
Another example is the unimolecular nucleophilic substitution (S N 1) reaction in organic chemistry, where it is the first, rate-determining step that is unimolecular. A specific case is the basic hydrolysis of tert-butyl bromide (t-C 4 H 9 Br) by aqueous sodium hydroxide. The mechanism has two steps (where R denotes the tert-butyl radical t-C ...
The kinetic order of any elementary reaction or reaction step is equal to its molecularity, and the rate equation of an elementary reaction can therefore be determined by inspection, from the molecularity. [1] The kinetic order of a complex (multistep) reaction, however, is not necessarily equal to the number of molecules involved.
The equilibrium approximation can sometimes be used in chemical kinetics to yield similar results to the steady state approximation. It consists in assuming that the intermediate arrives rapidly at chemical equilibrium with the reactants. For example, Michaelis-Menten kinetics can be derived assuming equilibrium instead of steady state ...
The result is equivalent to the Michaelis–Menten kinetics of reactions catalyzed at a site on an enzyme. The rate equation is complex, and the reaction order is not clear. In experimental work, usually two extreme cases are looked for in order to prove the mechanism. In them, the rate-determining step can be: Limiting step: adsorption/desorption
The result is in fact an exponential growth, thus giving rise to explosive increases in reaction rates, and indeed to chemical explosions themselves. This was the first proposal for the mechanism of chemical explosions. A quantitative chain chemical reaction theory was created later on by Soviet physicist Nikolay Semyonov in 1934. [3]
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