Kinetics Assignment - Reaction Orders

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SUMMARY

The discussion focuses on determining the reaction order and calculating the rate constant (k) and half-life (t1/2) for a first-order reaction involving reactant A. The user successfully plotted concentration data against time, confirming first-order kinetics with an R² value of 0.997. However, confusion arises when attempting to apply the integrated rate equation, specifically regarding the relationship between the constant rate constant (k) and the changing concentration of A over time. The user needs clarification on how to derive k from the gradient of the linear plot.

PREREQUISITES
  • Understanding of first-order reaction kinetics
  • Familiarity with integrated rate equations
  • Ability to interpret linear regression results
  • Knowledge of calculating half-life for first-order reactions
NEXT STEPS
  • Calculate the rate constant (k) using the gradient of the concentration vs. time plot
  • Determine the half-life (t1/2) for the first-order reaction using the formula t1/2 = 0.693/k
  • Learn about the integrated rate law for first-order reactions
  • Explore graphical methods for analyzing reaction kinetics
USEFUL FOR

Chemistry students, educators, and anyone studying reaction kinetics who seeks to understand first-order reactions and their mathematical representations.

sltungle
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Homework Statement



The concentration of the reactant A has been studied as a function of time. By a suitable plot of the data below, show that the reaction is first order, and determine the rate constant, k, and the half-life, t1/2. Use the integrated rate equation to determine [A] when t = 600s.

t (seconds) 100 200 300 400 500

[A] (mol/L) 0.344 0.314 0.286 0.261 0.238

Homework Equations



-d[A]/dt = k*[A]

The Attempt at a Solution



The main part that's confusing me is the bolded part. I've done the first part in showing that the reaction is first order by plotting the concentration on the Y-axis against time on the X-axis. My linear trend line has an R2 value of 0.997 so I'd say it's a safe bet to assume just from the geometry of the graph that the reaction is a first order one.

The second part (the bolded part) is what is stumping me, because I KNOW it's insanely simple but for some reason I can't do it.

I took the gradient of my graph (2.65*10-4) which is the reaction rate (d[A]/dt) and set that to equal k[A], but here's where I'm getting frustrated and things don't seem to be working out.

My gradient is a constant value (which makes sense - it's a linear graph); it doesn't depend on any variables. My [A] value is constantly changing as the reaction progresses over time.

If d[A]/dt = k*[A] and the left hand side is constant, while on the right hand side [A] is changing over time, then does k not also have to be a changing value in order to keep the whole equation constant? But that makes no sense, because k is a reaction rate constant. I need a solid value for it.

Any help would be greatly appreciated. I'm getting myself in a really bad mood over this and I get the feeling that by focusing too much on this one aspect of the problem that I'm blinding myself to alternate methods.
 
Physics news on Phys.org
\frac {d[A]} {dt} is not constant. Concentration changes by 0.030M in the first 100 sec and by 0.023M in the last 100 sec.
 

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