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  1. Rate equation - Wikipedia

    en.wikipedia.org/wiki/Rate_equation

    Rate equation. In chemistry, the rate equation (also known as the rate law or empirical differential rate equation) is an empirical differential mathematical expression for the reaction rate of a given reaction in terms of concentrations of chemical species and constant parameters (normally rate coefficients and partial orders of reaction) only ...

  2. Reaction rate constant - Wikipedia

    en.wikipedia.org/wiki/Reaction_rate_constant

    In chemical kinetics, a reaction rate constant or reaction rate coefficient (⁠ ⁠) is a proportionality constant which quantifies the rate and direction of a chemical reaction by relating it with the concentration of reactants. [1] For a reaction between reactants A and B to form a product C, a A + b B → c C. where.

  3. Arrhenius equation - Wikipedia

    en.wikipedia.org/wiki/Arrhenius_equation

    So, when a reaction has a rate constant that obeys the Arrhenius equation, a plot of ln k versus T −1 gives a straight line, whose gradient and intercept can be used to determine E a and A. This procedure has become so common in experimental chemical kinetics that practitioners have taken to using it to define the activation energy for a ...

  4. Steady state (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Steady_state_(chemistry)

    The steady state approximation, [1] occasionally called the stationary-state approximation or Bodenstein's quasi-steady state approximation, involves setting the rate of change of a reaction intermediate in a reaction mechanism equal to zero so that the kinetic equations can be simplified by setting the rate of formation of the intermediate equal to the rate of its destruction.

  5. Rate-determining step - Wikipedia

    en.wikipedia.org/wiki/Rate-determining_step

    Rate-determining step. In chemical kinetics, the overall rate of a reaction is often approximately determined by the slowest step, known as the rate-determining step (RDS or RD-step[1] or r/d step[2][3]) or rate-limiting step. For a given reaction mechanism, the prediction of the corresponding rate equation (for comparison with the experimental ...

  6. Plateau principle - Wikipedia

    en.wikipedia.org/wiki/Plateau_Principle

    Plateau principle. The plateau principle is a mathematical model or scientific law originally developed to explain the time course of drug action (pharmacokinetics). [1] The principle has wide applicability in pharmacology, physiology, nutrition, biochemistry, and system dynamics. It applies whenever a drug or nutrient is infused or ingested at ...

  7. Michaelis–Menten kinetics - Wikipedia

    en.wikipedia.org/wiki/Michaelis–Menten_kinetics

    In biochemistry, Michaelis–Menten kinetics, named after Leonor Michaelis and Maud Menten, is the simplest case of enzyme kinetics, applied to enzyme-catalysed reactions of one substrate and one product. It takes the form of a differential equation describing the reaction rate (rate of formation of product P, with concentration ) to , the ...

  8. Transition state theory - Wikipedia

    en.wikipedia.org/wiki/Transition_state_theory

    Using the Eyring equation, there is a straightforward relationship between ΔG ‡, first-order rate constants, and reaction half-life at a given temperature. At 298 K, a reaction with ΔG ‡ = 23 kcal/mol has a rate constant of k ≈ 8.4 × 10 −5 s −1 and a half life of t 1/2 ≈ 2.3 hours, figures that are often rounded to k ~ 10 −4 s ...