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  2. Rate equation - Wikipedia

    en.wikipedia.org/wiki/Rate_equation

    If the concentration of a reactant remains constant (because it is a catalyst, or because it is in great excess with respect to the other reactants), its concentration can be included in the rate constant, leading to a pseudo–first-order (or occasionally pseudo–second-order) rate equation. For a typical second-order reaction with rate ...

  3. Rate-determining step - Wikipedia

    en.wikipedia.org/wiki/Rate-determining_step

    In fact, however, the observed reaction rate is second-order in NO 2 and zero-order in CO, [5] with rate equation r = k[NO 2] 2. This suggests that the rate is determined by a step in which two NO 2 molecules react, with the CO molecule entering at another, faster, step. A possible mechanism in two elementary steps that explains the rate ...

  4. Euler method - Wikipedia

    en.wikipedia.org/wiki/Euler_method

    For this reason, the Euler method is said to be a first-order method, while the midpoint method is second order. We can extrapolate from the above table that the step size needed to get an answer that is correct to three decimal places is approximately 0.00001, meaning that we need 400,000 steps.

  5. Order of accuracy - Wikipedia

    en.wikipedia.org/wiki/Order_of_accuracy

    Consider , the exact solution to a differential equation in an appropriate normed space (, | | | |). Consider a numerical approximation u h {\displaystyle u_{h}} , where h {\displaystyle h} is a parameter characterizing the approximation, such as the step size in a finite difference scheme or the diameter of the cells in a finite element method .

  6. Lindemann mechanism - Wikipedia

    en.wikipedia.org/wiki/Lindemann_mechanism

    The steady-state rate equation is of mixed order and predicts that a unimolecular reaction can be of either first or second order, depending on which of the two terms in the denominator is larger. At sufficiently low pressures, k − 1 [ M ] ≪ k 2 {\displaystyle k_{-1}[{\ce {M}}]\ll k_{2}} so that d [ P ] / d t = k 1 [ A ] [ M ...

  7. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    The rate of an S N 2 reaction is second order, as the rate-determining step depends on the nucleophile concentration, [Nu −] as well as the concentration of substrate, [RX]. [1] r = k[RX][Nu −] This is a key difference between the S N 1 and S N 2 mechanisms.

  8. Effective molarity - Wikipedia

    en.wikipedia.org/wiki/Effective_molarity

    In chemistry, the effective molarity (denoted EM) [1] is defined as the ratio between the first-order rate constant of an intramolecular reaction and the second-order rate constant of the corresponding intermolecular reaction (kinetic effective molarity) [1] [2] or the ratio between the equilibrium constant of an intramolecular reaction and the equilibrium constant of the corresponding ...

  9. Continuous stirred-tank reactor - Wikipedia

    en.wikipedia.org/wiki/Continuous_stirred-tank...

    Plugging in the first CSTR equation to the second: = (+) Therefore for m identical CSTRs in series: C A m = C A o ( 1 + k τ ) m {\displaystyle C_{Am}={\frac {C_{Ao}}{(1+k\tau )^{m}}}} When the volumes of the individual CSTRs in series vary, the order of the CSTRs does not change the overall conversion for a first order reaction as long as the ...