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
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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
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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
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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
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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
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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
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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
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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
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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
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