(f ) We use the straight-line plot in Figure 16-8c to find the value of the rate constant for
this first-order reaction from the relationship
slopeak or k
To determine the slope of the straight line, we pick any two points, such as Pand Q,on
the line. From their coordinates, we calculate
slope0.300 min^1
k0.300 min^1
You should now work Exercises 44 and 45.
The graphical interpretations of concentration-versus-time data for some common
reaction orders are summarized in Table 16-3.
0.300 min^1
1
slope
a
(1.83)(0.27)
(8.501.50) min
change in ordinate
change in abscissa
slope
a
16-4 Concentration versus Time: The Integrated Rate Equation 675
Problem-Solving Tip:Some Warnings About the Graphical Method
for Determining Reaction Order
1.If we were dealing with real experimental data, there would be some error in each
of the data points on the plot. For this reason, we should notuse experimental data
points to determine the slope. (Random experimental errors of only 10% can intro-
duce errors of more than 100% in slopes based on only two points.) Rather we
should draw the best straight line and then use points on that line to find its slope.
Errors are further minimized by choosing points that are widely separated.
2.Remember that the ordinate is the vertical axis and the abscissa is the horizontal
one. If you are not careful to keep the points in the same order in the numerator
and denominator, you will get the wrong sign for the slope.
TABLE 16-3 Graphical Interpretations for Various Orders of the Reaction
aAnProducts
Order
Zero First Second
Plot that gives straight line [A] vs. t ln [A] vs. t vs. t
Direction of straight-line slope down with time down with time up with time
Interpretation of slope ak ak ak
Interpretation of intercept [A] 0 ln [A] 0
1
[A] 0
1
[A]