Applications Of Aqueous Equilibria Flashcards

1
Q

Common Ion Effect - Le Chateleier principle

A
  • 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
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2
Q

Common ion effect - qualitative effect on ph

A
  • decreases solubility of a solute
  • adding more conjugate ions may shift the ph
    See notes
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3
Q

Buffering capacity

A
  • 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
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4
Q

Henderson-Hasselbach equation

A

pH=pKa+log([conj.base]/[conj.acid])
pH=pKa+log([A-]/[HA])

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5
Q

Henderson-Hasselbach limitations

A
  • 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
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6
Q

Solubility product & solubility

A

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

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7
Q

Comparing solubilities of 2 different ionic solids

A
  • 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
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8
Q

Points on a titration curve

A

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

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