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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 ...
When one contrasts this with a dissonant interval such as a tritone (not tempered) with a frequency ratio of 7:5 one gets, for example, 700 − 500 = 200 (1st order combination tone) and 500 − 200 = 300 (2nd order). The rest of the combination tones are octaves of 100 Hz so the 7:5 interval actually contains four notes: 100 Hz (and its ...
[a] The bass and treble controls in a hi-fi system are each a first-order filter in which the balance of frequencies above and below a point are varied using a single knob. A special case of first-order filters is a first-order high-pass or low-pass filter in which the 6 dB per octave cut of low or high frequencies extends indefinitely.
A second-order filter decreases at −12 dB per octave, a third-order at −18 dB and so on. Butterworth filters have a monotonically changing magnitude function with ω {\displaystyle \omega } , unlike other filter types that have non-monotonic ripple in the passband and/or the stopband.
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.
The simple first-order roll-off also provides only very mild reduction of rumble, [11] and many manufacturers consider that turntables, arm, and cartridge combinations should be of sufficient quality for problems not to arise. Some manufacturers follow the IEC standard, others do not, while the remainder make this IEC-RIAA option user selectable.
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 .
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 ...