DGP Kinetics Flashcards
Rate is always _
POSITIVE
What is the only way the rate law can be determined?
EXPERIMENTALLY
In a first order reaction, if you halve the reactant concentration, the rate _
HALVES
In a first order reaction the rate is directly proportional to the concentration of the reactant
i.e. rate ∝ [A]
In a second order reaction, if you halve the reactant concentration, the rate _
QUARTERS
This is because: rate ∝ [A]^2
Differential rate law provides rate at a _
particular instant where the reaction mixture has a particular composition
Integrated rate law is an _
expression that gives the concentration of a species as a function of time. It can also be used to establish the order of a reaction and then it’s rate constant, k.
What are the two methods of determining the rate law from experimental data?
- Using the initial rate method (differential rate law, i.e. rate vs. concentration data)
- Using the method of integration (integrated rate law, i.e. concentration vs. time data)
Steps in method of integration for finding the rate law
- Postulate an order of the reaction (first, second, …)
- Derive an expression for the variation of concentration vs. time (i.e. integrated rate law)
- Manipulate expression to linear form (i.e. linearise integrated rate law using ln)
- Plot data to check if original postulate is correct (know the concentration vs. time graph shapes for zero, first, and second order reactions_
- If correct => derive k
(If not correct return to step 1)
What method do you use to find the rate law when you have a reaction in the form A + B -> products?
Method of isolation:
Essentially use two repeats of the experiment where each is alternatively in excess to determine a “pseudo-order of the reaction for one of the reactants. Then you plot the ln[A] graph for each to confirm).
What does the “A” mean in the Arrhenius equation?
A = Arrhenius factor or pre-exponential factor. It has the same units as k (the rate constant) and is a measure of frequency of collisions in the correct orientation for reaction.
A high Ea (activation energy) VALUE corresponds to a reaction is very _ to _
very SENSITIVE to CHANGES OF TEMPERATURE
Steps to determine Ea and A for a reaction
1) Convert T from celsius to Kelvin (+273.15)
2) Calculate ln(k)
3) Calculate 1/T from absolute T
4) Plot lnk vs. 1/T
5) Calculate slope = -Ea/R
6) Calculate A from y-intercept (0, lnA) or using Ea determined from data and two sets of (K, T) data points: