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Energy profile diagram for kinetic versus thermodynamic product reaction. Thermodynamic reaction control or kinetic reaction control in a chemical reaction can decide the composition in a reaction product mixture when competing pathways lead to different products and the reaction conditions influence the selectivity or stereoselectivity.
A reaction coordinate diagram can also be used to qualitatively illustrate kinetic and thermodynamic control in a reaction. Figure 9:Kinetic and Thermodynamic Control: A. Product B is both the kinetic and thermodynamic product and B. Product A is the kinetic product while B is the thermodynamic product. [4]
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.
Non-equilibrium thermodynamics is a branch of physics that studies the dynamics of statistical ensembles of molecules via unstable states. Being "stuck" in a thermodynamic trough without being at the lowest energy state is known as having kinetic stability or being kinetically persistent.
Instead of balancing chemical reactions and constructing Eh-pH diagrams by hand, for example, students can spend time exploring advanced topics like multi-component equilibrium, kinetic theory, or reactive transport. [20] A free download of The Geochemist's Workbench Community Edition is available from the developer's website. [6]
The main feature of thermodynamic diagrams is the equivalence between the area in the diagram and energy. When air changes pressure and temperature during a process and prescribes a closed curve within the diagram the area enclosed by this curve is proportional to the energy which has been gained or released by the air.
The ideal kinetic resolution is that in which only one enantiomer reacts, i.e. k R >>k S. The selectivity (s) of a kinetic resolution is related to the rate constants of the reaction of the R and S enantiomers, k R and k S respectively, by s=k R /k S, for k R >k S. This selectivity can also be referred to as the relative rates of reaction.
Cycle Compression, 1→2 Heat addition, 2→3 Expansion, 3→4 Heat rejection, 4→1 Notes Power cycles normally with external combustion - or heat pump cycles: ; Bell Coleman