Applications Of Aqueous Equilibria Flashcards
Common Ion Effect - Le Chateleier principle
- adding another substance with an ion in the equilibrium expression will cause a rxn to shift according to Le chatelier principle
- shift favors the solid or deionized form
See notes
Common ion effect - qualitative effect on ph
- decreases solubility of a solute
- adding more conjugate ions may shift the ph
See notes
Buffering capacity
- the capacity in which a buffer can weaken the effect of H+ or OH- ions to resist change in a rxn
- larger [HA] and A- = larger buffering capacity
- [HA]=A- for best buffering capacity in both directions
pH=pKa+log([base]/[acid])
[base]=[acid])=1 log(1)=0
Henderson-Hasselbach equation
pH=pKa+log([conj.base]/[conj.acid])
pH=pKa+log([A-]/[HA])
Henderson-Hasselbach limitations
- soln needs to be buffered (if not use ICE table)
- assumes NO ionization of HA & A
- only a good assumption if enough of Conj so that common ion effect shuts down ionization in both directions
Solubility product & solubility
Solubility: max amt of solute to the soln can hold under the given conditions
(molar solubility=max molarity possible)
Solubility product (constant): Ksp, equilibrium constant for the dissolution of an ionic solid
Ksp=[A]^a[B]^b
Comparing solubilities of 2 different ionic solids
- can always compare solubilities to see which is more soluble
- you can only compare Ksp values IE dissociates into the same #s of ions so that the relationship between Ksp & X are the same
See notes
Points on a titration curve
See notes
Check if it is buffered, what is the determined pH of the soln, and how to calculate the pH
Zero point, 1/4 point, 1/2 point, 1st eq pt, 2nd 1/2 eq pt, 3/4 between 1&2 eq pt, 2nd eq pt, pH at flattened at pt after 2nd eq pt