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Definitions and equations
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solubility
amount of substance that will dissolve in a given amount of solvent
Ks definition
solubility product constant. a large Ks value means high solubility
PH to H3O+
shift log - PH
H3O+ to PH
-log H3O+
H3O+ to OH-
1 × 10-14 / H3O+
OH- to H3O+
1 × 10-14 / OH-
OH- to POH
-log OH-
POH to OH-
shift log - POH
POH to PH
14 - POH
PH to POH
14 - PH
Kw
1 × 10-14
dilution factors equation
[new] = volume used / total volume x [original]
common ion effect
adding a common ion increases its concentration in the solution which shifts equilibrium to create more product reducing solubility
predicting precipitation
Q<Ks = no precipitate
Q=Ks = no precipitate
Q>Ks = precipitate
effect of acidic conditions on solubility
When put with a base H3O+ neutralizes OH- so [OH-] decreases. equilibrium shifts to make more OH- so solubility increases
effect of complex ions on solubility
if a complex ion can be formed ions will be removed from the solution to create a complex ion. So concentration o ion will decrease and equilibrium will shift to produce more of that ion increasing solubility
Ka
acid dissociation constant
Kb calculation
Kb = Kw/Ka
[OH-] from Kb
[OH-] = square root of Kb x [A-]
conductivity of solutions
strong acid has increased conductivity due to it completely dissociating in water. This means that lots of charged ions are available making it a good electrolyte
Kc
equilibrium constant
Kc equation
products/reactants
Le chatelier’s principle
If you make a change to an equilibrium system the equilibrium will shift to minimize the change
Buffer solutions
Is made of a weak acid and its conjugate base or a weak base and it conjugate acid. It will resist changes in PH when small amounts of acid or base are added.
Henderson equation
PH = pKa + log [base]/[acid]
effectiveness of buffer solutions
PH<pKa more effective at overcoming addition of excess base
PH=pKa weak acid and conjugate base or weak base and conjugate acid are equal in concentration. the buffer is equally effective
PH>pKa more effective at overcoming addition of excess acid
equivalence point
equal amounts of acid and base. halfway up steepest point of curve
buffer zone
between initial point and equivalence point
indicators
show when equivalence point is reached. pKa of the indicator should be ± 1 between PH at the equivalence point
CO3 ion
CO32-
CrO4 ion
CrO42-
SO4 ion
SO42-
CO3 ion
CO32-
CIO3 ion
CIO3 -
NO3 ion
NO3-
PO4
PO43-