Integrating the differential rate equation

In summary: A]_0}^{[A]} \frac{[A]}{[A]}d[A] or even better, giving an actual name to the variable of integration, \int_{[A]_0}^{[A]} \frac{[A]}{[A]}d[t] or \int_{[A]_0}^{[A]} \frac{[A]}{[A]}d[\tau] or whatever.
  • #1
mycotheology
89
0
Heres the differential rate equation for a 0 order reaction in chemistry:
[itex]Rate = {{-d[A]} / {dt}} = k[/itex]
which can be rearranged to this:
[itex]-d[A] = dt k[/itex]
and when you integrate this you get the integrated rate equation but I don't understand how this works. The site I'm reading says you integrate both sides of the equation and get this:
http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/Grafik/ord_z5.gif
is that supposed to be a definite integral or something? Anyhow, after integrating they get this:
http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/Grafik/ord_z3.gif
I don't get it. Firstly [A] and t are variables so shouldn't they be raised a power and get divided by 2? In other words, shouldn't they become [itex][A]^{2} / 2[/itex] and [itex]t^{2} / 2[/itex]? Secondly, what's going on with the d. d means the change in something but I've never seen it been integrated before so I don't know what happens to it. Why did it disappear?

The 1st order equation has me equally confused:
http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/Grafik/ord1_ip1.gif
integratin that, they get this:
http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/Grafik/ord1-3.gif
has does d[A]/[A] become ln[A]?
 
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  • #2
mycotheology said:
Heres the differential rate equation for a 0 order reaction in chemistry:
[itex]Rate = {{-d[A]} / {dt}} = k[/itex]
which can be rearranged to this:
[itex]-d[A] = dt k[/itex]
and when you integrate this you get the integrated rate equation but I don't understand how this works. The site I'm reading says you integrate both sides of the equation and get this:
http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/Grafik/ord_z5.gif
is that supposed to be a definite integral or something?

Any time there are limits of integration it is a definite integral.

Anyhow, after integrating they get this:
http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/Grafik/ord_z3.gif
I don't get it. Firstly [A] and t are variables so shouldn't they be raised a power and get divided by 2? In other words, shouldn't they become [itex][A]^{2} / 2[/itex] and [itex]t^{2} / 2[/itex]? Secondly, what's going on with the d. d means the change in something but I've never seen it been integrated before so I don't know what happens to it. Why did it disappear?

You need to remember back to your Calc I/II days. The d means an infitessimal change, you covered this when going over Riemann sums in Calc I. In more general terms, the d term let's you know for what term you are integrating with respect to. dx means you are integrating with respect to x and all other variables are held constant.

##\int x \ dx = \frac{x^2}{2} + C## because the variable you are integrating with respect you is x. However, ##\int y \ dx = xy + C## because y is held constant.

So, in this problem we have ##\displaystyle \int_{[A]_0}^{[A]} d[A] = -k \int_{t_o}^{t} dt## We are simply integrating the constant 1 in both of these equations, so the integral yields ##[A]## and t respectively, evaluated at the proper limits of integration.

##\displaystyle \int_{[A]_0}^{[A]} d[A] = -k \int_{t_o}^{t} dt## yields ##[A] - [A]_0 = -k (t - t_0)##. In these types of problems, ##t_0## is usually 0 so the equation simplifies to ##[A] = -kt + C##. I believe the + C term is the initial amount of the concentration of A, we never wrote it like this, we kept the ##[A]_0## term in the equation.

The 1st order equation has me equally confused:
http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/Grafik/ord1_ip1.gif
integratin that, they get this:
http://www.uni-regensburg.de/Fakultaeten/nat_Fak_IV/Organische_Chemie/Didaktik/Keusch/Grafik/ord1-3.gif
has does d[A]/[A] become ln[A]?

Remember ##\displaystyle \int \frac{1}{x} dx = ln|x| + C##.
 
  • #3
[tex]\int_{[A]_0}^{[A]} \frac{d[A]}{[A]}[/tex]
is just bad notation. Although it is, unfortunately, often done you should NOT use the same symbol for the "variable of integration" and the limits of integration. Better would be
[tex]\int_{[A]_0}^{[A]} \frac{dt}{t}[/tex]
 

Related to Integrating the differential rate equation

1. What is the differential rate equation?

The differential rate equation is a mathematical expression that describes the rate of change of a chemical reaction with respect to time. It is commonly used in chemical kinetics to determine the rate of a reaction based on the concentration of reactants.

2. How is the differential rate equation derived?

The differential rate equation is derived from the rate law, which is an experimentally determined equation that relates the rate of a reaction to the concentrations of its reactants. The differential rate equation is obtained by taking the derivative of the rate law with respect to time.

3. What is the significance of integrating the differential rate equation?

Integrating the differential rate equation allows us to determine the concentration of reactants or products at any point in time during a chemical reaction. This information is useful in understanding the progress of a reaction and predicting its outcome.

4. How do you integrate the differential rate equation?

The process of integrating the differential rate equation involves solving for the concentration of a reactant or product using calculus techniques. This involves finding the antiderivative of the differential rate equation and applying initial conditions to solve for any unknown constants.

5. What are some limitations of using the differential rate equation?

The differential rate equation assumes that the reaction is taking place under ideal conditions, such as constant temperature and pressure. It also assumes that the reaction is following a specific order, and it may not be accurate for reactions that deviate from this order. Additionally, the differential rate equation does not take into account any competing reactions or catalysts that may affect the rate of the reaction.

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