First, write the differential form of the rate law.
Rearrange to give:
Second, integrate both sides of the equation.
Recall from calculus that:
Upon integration,
Rearrange to solve for [A] to obtain one form of the rate law:
This can be rearranged to:
This can further be arranged into y=mx +b form:
and y-intercept b:
Now, recall from the laws of logarithms that
where [A] is the concentration at time t and [A]o is the concentration at time 0, and k is the first-order rate constant.
Because the logarithms of numbers do not have any units, the product −kt also lacks units. This concludes that unit of k in a first order of reaction must be time-1. Examples of time-1 include s-1 or min-1. Thus, the equation of a straight line is applicable:
To test if it the reaction is a first-order reaction, plot the natural logarithm of a reactant concentration versus time and see whether the graph is linear. If the graph is linear and has a negative slope, the reaction must be a first-order reaction.
To create another form of the rate law, raise each side of the previous equation to the exponent, e:
Simplifying gives the second form of the rate law:
The integrated forms of the rate law!
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