Equilibrium principles in aqueous systems

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36 Terms

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solubility

amount of substance that will dissolve in a given amount of solvent

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Ks definition

solubility product constant. a large Ks value means high solubility

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PH to H3O+

shift log - PH

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H3O+ to PH

-log H3O+

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H3O+ to OH-

1 × 10-14 / H3O+

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OH- to H3O+

1 × 10-14 / OH-

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OH- to POH

-log OH-

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POH to OH-

shift log - POH

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POH to PH

14 - POH

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PH to POH

14 - PH

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Kw

1 × 10-14

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dilution factors equation

[new] = volume used / total volume x [original]

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common ion effect

adding a common ion increases its concentration in the solution which shifts equilibrium to create more product reducing solubility

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predicting precipitation

Q<Ks = no precipitate

Q=Ks = no precipitate

Q>Ks = precipitate

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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

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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

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Ka

acid dissociation constant

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Kb calculation

Kb = Kw/Ka

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[OH-] from Kb

[OH-] = square root of Kb x [A-]

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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

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Kc

equilibrium constant

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Kc equation

products/reactants

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Le chatelier’s principle

If you make a change to an equilibrium system the equilibrium will shift to minimize the change

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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.

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Henderson equation

PH = pKa + log [base]/[acid]

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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

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equivalence point

equal amounts of acid and base. halfway up steepest point of curve

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buffer zone

between initial point and equivalence point

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indicators

show when equivalence point is reached. pKa of the indicator should be ± 1 between PH at the equivalence point

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CO3 ion

CO32-

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CrO4 ion

CrO42-

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SO4 ion

SO42-

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CO3 ion

CO32-

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CIO3 ion

CIO3 -

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NO3 ion

NO3-

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PO4

PO43-