Deck 5: equilibria Flashcards

(23 cards)

1
Q

definition of dynamic equilibrium

A

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

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2
Q

graphs to represent equilibrium conc time and rate time

A

check notes (one for concentration, mol dm-3, one for rate of reaction, mol dm-3 s-1)

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3
Q

LCP definition

A

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

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3
Q

what is Qc and Kc

A

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)

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3
Q

How is Kp different from Kc

A

Kc use conc and Kp use partial pressure

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4
Q

what is kf and kb
relationship between Kf and Kb and Kc

A

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

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5
Q

what is the overall Kc for reaction with multiple smaller reactions

A

product of Kc for each reaction

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6
Q

Kc for reaction where the stoichiometric coefficients of a balanced equation are multiplied by a factor n

A

new Kc = K^n

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7
Q

when can water be excluded from the eqm constant

A

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)

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8
Q

definition of degree of dissociation

A

the fraction of reactant that has dissociated at a particular temperature

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9
Q

homo vs hetero eqm

A

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

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10
Q

what can be included for Kc and Kp of hetero eqm

A

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

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11
Q

ΔG at eqm

A

ΔG = 0

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12
Q

formula for ΔG relating K and what its signs mean

A

ΔG⦵ = -RT ln K

when ΔG⦵<0, K >1 and poe lies more right

when ΔG⦵ > 0, K <1 and poe lies more left

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13
Q

just read

A

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

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14
Q

think about LCP change in conc graph

A

refer to notes if needed

14
Q

think about LCP change in TOTAL pressure graph

A

refer to notes if needed
rmb all partial pressures increase at the start

15
Q

effect of change in volume on rate of reaction

A

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

16
Q

effect of change in temperature on rate of reaction

A

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

17
Q

addition of catalyst on eqm

A

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

18
Q

what is the haber process equation is it exo or endo

A

N2 + 3H2 reversible arrow 2NH3

exo

19
Q

conditions for haber process

A
  1. moderately high temp 450˚C
    - since forward is exo, low temp will lead to higher yield
    - but too slow at low temp
    - but high temp means lower yield and higher cost so compromise made
  2. 200atm
    - high pressure favour forward reaction but cost of production increase and dangerous
    - compromise to moderate pressure
  3. catalyst of finely divided iron catalyst with aluminium oxide promoter
    - increase production rate and yield not affected
  4. continued removal of ammonia
    - shift eqm position to the right and increase yield of ammonia
    - through cooling of reaction to liquefy ammonia
  5. keep molar ratio of N2 and H2 to 1:3
    - minimise excess
20
Q

effect of adding inert gas as constant vol or at constant pressure

A

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