
Marita E. answered 10/02/23
PhD in Chemistry/Biochemistry with 8+ years teaching experience
To answer this, realize that the rate equation takes the form
rate= k[A]n[B]m eq (1)
n and m have no relationship to the coefficients of the reactants, A and B in the balanced equation. They must be experimentally determined. They are called the order of the reaction with respect to A and B, respectively. Looking at the data, you can clearly see that the reaction rate does not depend on [B] because it remains the same even if [B] doubles. Therefore, the reaction is zero order with respect to B. That is, m=0. To get the order with respect to a, use eqn 1 for trials 1 & 3. These two trials show you the variation of rate with respect to A.
rate3/rate1 = [A]3/[A]1 note that k is present in both numerator and denominator on the right side of this ratio and so will cancel out.
,0960/.0240 = (.4)n/(.2)n gives you the condition that 4 = 2n therefore n must be 2. The reaction is second order in A. So your rate equation is
rate = k[A]2
To get k, pick any trial (or if you are feeling industrious, do this process for all three trials and take the average k) and substitute the values for rate and [A] to get k.
Let's set up the equation for trial 1:
.0240 M/sec = k[0.200 M]2 You should be able to solve for k from this equation. I will leave you to carry out the math.
Treat the units the same way you do the numbers. The units of k will be (M/sec)/ M2 = 1/M-sec
To verify your answer for k, try doing another trial and see if you get the same k. You should.