Equilibrium Flashcards

1
Q

Why is a dynamic equilibrium so called?

A

The forward and back reactions are still happening but their rates are balanced, so the amounts of each substance in the mixture do not change.

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2
Q

Approach to equilibrium:-

A

Assume that left is A and right is B. Initially no A- forward = zero. Lots of B so relatively fast back reaction.
A starts to form so forward reaction now starts, rate increasing relative to amount of A. Simultaneously, B amount will decrease and thus so will back reaction rate. Eventually reaction rates equalise and amounts of A and B stop changing. Equilibrium has been established.

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3
Q

Equilibrium constant:-

A

Function of conc of each component of reaction mixture.

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4
Q

Composition of an equilibrium mixture generally depends on:-

A

How favourable the forward reaction is compared to the reverse reaction and how much of each substance was initially present.

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5
Q

Key features of Kc:- (3)

A
  • Kc has a fixed value for any particular reaction at a given temp, independent of starting comp or other variables.
  • Kc expression value computed from concs in mixture will not equal Kc if mixture isn’t at equilibrium.
  • Kc changes when temp changes.
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6
Q

Kc units:-

A

Add up powers in top line or Kc expression and subtract powers on bottom line. Call this X. Units are mol^(x)dm^-(3x). If mols are equal on either side of equation, conc units will cancel out and so Kc will have no units.

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7
Q

Calculating Kc from experimental data:-

A

Generally difficult to measure all concs in subsfance so usual approach is to start with mixture where we know initial concs and measure the change in conc of one reactant, then use equation for the redt.

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8
Q

Examples of ways to follow conc change:- (3)

A
  • change in absorption of light, if one substance is coloured.
  • pH change, if one is acid/alkali.
  • titration, provided time taken for titration is short compared to the time taken for equilibrium to shift.
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9
Q

Knowing when equilibrium is reached:-

A

Parameter being measured will stop changing.

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10
Q

Value of Kc interpretation:-

A

Higher Kc = further to the right equilibrium = greater yield.

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11
Q

Changing temp effect on equilibria:-

A

Kc decreases for exothermic as temp rises, increases for endo.

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12
Q

Temp equilibrium shift:-

A

Increase = shift in endothermic direction (since this will take away heat and oppose the change).

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13
Q

Catalyst on equilibria:-

A

No effect as both rates increase.

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14
Q

Pressure on Kc:-

A

No change.

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15
Q

Heterogeneous equilibria:-

A

Solutions + gases included in Kc, solids and liquids not.

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16
Q

Mole fraction:-

A

Moles of X/total moles of all substances

17
Q

Partial pressure:-

A

The pressure a gas would exert were it the only one present.

18
Q

Kp equation:-

A

P products divided by p reactants. P is to the power of how many moles the substance is. No brackets. Only gases usef.

19
Q

Partial pressure equation:-

A

Px = mole fraction of A x total pressure

20
Q

Kp units:-

A

Top - bottom powers for power. Units = atm^ , Pa^ or kPa^

21
Q

Kp value:-

A
  • depends only on temp.

* bigger value = further to right.