Topic 6: Chemical Kinetics Flashcards
Rate of rxn
the change in conc of reactants/products per unit time
unit: mol dm-3 s-1
rate of rxn equation
rate of rxn = Δ conc / time taken
- conc can either be product or reactant
technique used to measure change in pH
using pH probe and a meter
technique used to measure change in conductivity
conductivity probe and a meter
as no of ions increase, electrical conductivity increases… and vice versa
technique used to measure change in mass
- reacting the mixture in a sealed beaker (e.g. cotton on the neck)
- having the beaker placed on a balance throughout the rxn
NOTE: will not work with H2 as its too light to give significant change in mass
technique used to measure change in vol of gas
- downward displacement of gas: only works on gases with low solubility in water
- OR connecting a gas syringe to a closed system (e.g. sealed beaker) and allowing pressure to push the syringe handle
technique to detect change in rxn
clock rxn
- measure for the rxn to reach a certain fixed point
- i.e. something observable that can be used as an arbitrary endpoint to stop the clock
technique to measure change in colour
- for rxns involving transition metals or other coloured compounds
- equipment may be colorimeter, of spectrophotometer
- works by passing light of a selected wavelength through the soln being studied, to a sensitive photocell
- the photocell generates a current depending on the light intensity, which in turn depends on the conc of the coloured reactant/product
- measures absorbance against time
collision theory
before a chem rxn can occur:
- the reactants must physically & directly collide
- reactants must have correct mutual orientation
- reacting particles must have sufficient KE to initiate the rxn (I.e. Ea, or activation energy)
- temp (in k) is proportional to avg KE of particles in a substance
factors affecting rate of rxn: temp
higher temp = higher KE = higher successful collisions = more particles achieve Ea = higher rate of rxn
many rxn speeds increase by 2x for every 10 degree C/K increase
Maxwell-Boltzmann energy distribution curve
a plot of the no of particles with a given KE, plotted against KE
factors affecting rate of rxn: concentration
higher conc = higher no of particles per unit area = higher no of successful collisions = higher no of reactants achieving Ea = higher rate of rxn
doubling the conc of one of the reactants typically doubles rate of rxn
factors affecting rate of rxn: particle size/SA
smaller particle size = bigger surface area = higher chance of contact = higher no of successful collisions = more reactants with Ea = higher rate of rxn
factors affecting rate of rxn: catalyst
- provides an alternate pathway with less Ea requirement
- in reversible rxns, catalysts equally affect both forward and backward rxns so it doesn’t alter equilibrium positions
homogeneous catalyst
same physical state as reactant
e.g. breakdown of O3 catalysed by chlorine