Kinetics Flashcards
1
Q
Reaction rate
A
- how quickly a reaction takes place (change in concentration of reactant or product over time)
- affected by concentration, surface area, pressure, temperature, or inclusion of a catalyst
- can be measured by change of gas volume of product over time, pH over time, mass over time, or colour
2
Q
Maxwell-Boltzmann
A
- peak of curve = most probable energy for any particle
- Area = total no. particles
- At lower temperatures, most likely energy will decrease so peak will move up and move backwards, but area will be the same
3
Q
Rate equation
A
- rate = rate constant (k)[A]^m[B]^n
- m and n are the orders of reaction for those reactants, they represent the effect its concentration has on the rate
- k only varies with temperature
- unit of rate can be calculated by cancelling the units of the products
- rate equation is determined experimentally
4
Q
Orders of reaction
A
- Zero order = [A]^0
- concentration of A has no effect on the rate, graph of rate against [A] is just a flat line
- First order = [A]^1
- concentration of A is directly proportional to Rate, graph is a straight line through origin with constant gradient
- Second order = [A]^2
- rate is proportional to concentration of A^2, graph is curved
- order of whole reaction = total of orders of all products
5
Q
Clock reactions
A
- a reaction where there is a sudden increase in the concentration of a product after a limiting reactant is used up, leading to an observable end point e.g colour change
- it must be assumed that concentrations don’t change, temperature is constant and the endpoint of the change is close to the endpoint of the reaction
6
Q
Iodine clock reaction
A
- sodium thiosulfate immediately reacts with any Iodine produced, but when it runs out the Iodine immediately turns the starch a blue-black colour
- transfer 25cm^3 of H2SO4 of known concentration to a beaker, add 20cm^3 water, and 1cm^3 starch
- measure the amount of potassium iodide of known conc. and add it to the beaker with 5cm^3 sodium thiosulfate
- add 10cm^3 of H2O2 last and simultaneously start a stop watch. Stir until it turns blue and record the time taken. Repeat with varying amounts of Potassium Iodide
7
Q
Rate determining step
A
- the step of the reaction with the slowest rate, if the mechanism involves multiple steps
- any species involved in the steps after the RDS will not be in the rate equation
- orders of reaction show how many moles of that reactant are involved in the RDS i.e ([A]^2 means 2 moles of A in RDS)
- catalysts will appear in the rate equation but not the chemical equation
8
Q
Arrhenius equation
A
- k = Ae^(-Ea/RT)
- rate constant = Arrhenius constante^(-Activation energy/Gas constanttemperature)
- ln(k) = ln(A)-Ea/RT can be plotted as a graph like y= mx + c on a graph of lnK against 1/Twith gradient of -Ea/R and y-intercept of lnA
9
Q
Gas equilibria
A
- gas equilibrium constant = Kp = same as equilibrium constant but instead of concentration partial pressure is used, used for reversible reactions in gas phase
- partial pressure = mole fraction of gas*total pressure of the mixture
- mole fraction of gas = number of moles in the gas/total number of moles of gas in the mixture
- is affected by Le Chateliers principle like normal equilibrium constant, changes in temperature affect it but not pressure or adding a catalyst