definition of dynamic equilibrium
dynamic equilibrium is a state in a reversible reaction within a closed system in which the forward and backwards reactions are continuing at the same rate, resulting in no net change in macroscopic properties (eg. concentration, partial pressure) of the reactants and products
graphs to represent equilibrium conc time and rate time
check notes (one for concentration, mol dm-3, one for rate of reaction, mol dm-3 s-1)
LCP definition
when a system in equilibrium is subjected to a change, the system will react to counteract the change imposed so as to reestablish the equilibrium
what is Qc and Kc
at any given time, the reaction quotient Qc is the ratio of the concentrations of reactants and products raised to their stoichiometric ratios
Qc = [C]^c[D]^d/[A]^a[B]^b
K is a measure of the extent of reaction
at equilibrium, Qc becomes constant and this value is Kc (ONLY DEPENDENT ON TEMP)
How is Kp different from Kc
Kc use conc and Kp use partial pressure
what is kf and kb
relationship between Kf and Kb and Kc
Kf is rate constant of rate of forward rxn
ratef= Kf[A]^a[B]^b
Kb is rate constant of rate of backwards reaction
Kc = Kf/Kb = [C]^c[D]^d/[A]^a[B]^b
what is the overall Kc for reaction with multiple smaller reactions
product of Kc for each reaction
Kc for reaction where the stoichiometric coefficients of a balanced equation are multiplied by a factor n
new Kc = K^n
when can water be excluded from the eqm constant
when water is used as a solvent (eg. in a reaction in aqueous medium and water is a reactant, conc of water can be taken to be approx. constant as it is present in large amounts)
definition of degree of dissociation
the fraction of reactant that has dissociated at a particular temperature
homo vs hetero eqm
homo: eqm system in which all the substances involved are in the same phase
hetero: eqam system in which the substances are not in the same phase
what can be included for Kc and Kp of hetero eqm
conc/partial pressure of pure solids and liquids as they are constant at a constant temp
conc of water when it is present in large amounts in an aqueous solution
ΔG at eqm
ΔG = 0
formula for ΔG relating K and what its signs mean
ΔG⦵ = -RT ln K
when ΔG⦵<0, K >1 and poe lies more right
when ΔG⦵ > 0, K <1 and poe lies more left
just read
collision theory for LCP
eg. if u add more reactant, frequency of effective collisions between reactants increase and rate of forward reaction increases where rate of forward > rate of backward until eqm is reestablished
think about LCP change in conc graph
refer to notes if needed
think about LCP change in TOTAL pressure graph
refer to notes if needed
rmb all partial pressures increase at the start
effect of change in volume on rate of reaction
when V increases, partial pressure of all gases decrease and since p is proportionate to concentration, concentration decreases and rate of both forward and backward reactions decrease
takes longer to reach eqm
effect of change in temperature on rate of reaction
when temp increases, the rate constants of both the forward and backward reaction increases as
k=Ae^-Ea/RT
the particles with energy greater than or equal to activation energy Ea increases and time to reach eqm decreases
addition of catalyst on eqm
lower activation energy of both forward and backward reaction to the same extent hence rate for both forward and backward reaction increased by the same extent and adding catalyst has no effect on eqm constant k and the composition of the eqm mixture
but eqm is reached more quickly
what is the haber process equation is it exo or endo
N2 + 3H2 reversible arrow 2NH3
exo
conditions for haber process
effect of adding inert gas as constant vol or at constant pressure
constant vol
- total pressure increase but partial pressures do not change so no change in K and eqm not affected
constant pressure
- total volume increase
- partial pressures decrease and eqm shift to produce more moles of gas