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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. 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 .

  5. 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.

  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. Order of approximation - Wikipedia

    en.wikipedia.org/wiki/Order_of_approximation

    First-order approximation is the term scientists use for a slightly better answer. [3] Some simplifying assumptions are made, and when a number is needed, an answer with only one significant figure is often given ("the town has 4 × 10 3, or four thousand, residents"). In the case of a first-order approximation, at least one number given is exact.

  8. Curve fitting - Wikipedia

    en.wikipedia.org/wiki/Curve_fitting

    The first degree polynomial equation = + is a line with slope a. A line will connect any two points, so a first degree polynomial equation is an exact fit through any two points with distinct x coordinates. If the order of the equation is increased to a second degree polynomial, the following results:

  9. Second derivative - Wikipedia

    en.wikipedia.org/wiki/Second_derivative

    The second derivative of a function f can be used to determine the concavity of the graph of f. [2] A function whose second derivative is positive is said to be concave up (also referred to as convex), meaning that the tangent line near the point where it touches the function will lie below the graph of the function.