1. Write equation
- state
- reversible arrow
- use mol or M according to the question
- normally product is 0 except
- it duels with changes after reaching equilibrium
- let the amt/conc. used be x (doesnt matter as long as 2 use the same unit)
- beware of the coefficient in front of x in the equation
- left - , right+ expect duels with changes after reaching equilibrium
([pdt conc.]^coefficient x [pdt conc.]^coefficient......)
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([react conc.]^coefficient x [react conc.]^coeffiecient......)
- If (2) use mole, divide mole by volume to get conc. here
- Unit= M^(pdt coeffiicient+pdt coefficient-react coefficient)
- substitute x
Kp
Principle:
Use mole fraction x total pressure to obtain partial pressure.
Partial pressure will understudy [pdt conc.] e.t.c.
Method
Add 'total mole' to step (2) and (3)
Add one step more after (3) for 'mole fraction'
*mole fraction = proportion of the gas inside(x100% becomes %)
Note:
- Increase in volume = decrease in concentration. (if both sides of the equation has same volume, e.g. H2 + I2 <----> 2HI, then no change in position of equilibrium, otherwise change.)
- Adding inert gas to increase the total pressure(V is constant) as no effect on the position of equilibrium since there is no change in concentration.
- When product is gas but reactant is solid/liquid, Kp =product x product and no division.