Chapter 16 Flashcards

1
Q

Buffer

A
  • Resists pH change by neutralizing added acid or added base.
  • Contains significant amounts of both a weak acid and it’s conjugate base (or weak base and conjugate acid)
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2
Q

Buffer Characteristics

A
  • Buffers resist pH change.
  • A buffer contains significant amounts of both a weak acid and its conjugate base.
  • The weak acid neutralizes added base.
  • The conjugate base neutralizes added acid.
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3
Q

Common Ion Effect

A

The tendency for a common ion to decrease the solubility of an ionic compound or to decrease the ionization of a weak acid or weak base.

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4
Q

Henderson-Hasselbalch Equation

A

An equation used to calculate the pH of a buffer solution from the initial concentrations of the
buffer components.

pH = pka + log( [base]/[acid] )

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5
Q

Calculating pH changes in buffer solution after adding small amounts of a strong acid or base

A
  1. Stoichiometry—use the stoichiometry of the neutralization equation to calculate the changes in the amounts (in moles) of the buffer components upon addition of the acid or base.
  2. Equilibrium—use the new amounts of buffer components to work an equilibrium problem to find pH. (For most buffers, this can also be done with the Henderson–Hasselbalch equation.)
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6
Q

Buffer Effectiveness

A

Buffer is most effective when:

  • Concentrations of acid and conjugate base are equal and high.
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7
Q

Buffer Range

A
  • Lowest pH for effective buffer occurs when the base is one-tenth as concentrated as the acid.
  • Highest pH for effective buffer occurs when the base is 10 times as concentrated as the acid.
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8
Q

Buffer Capacity

A

The amount of acid or base that you can add to a buffer without causing a large change in pH.

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9
Q

Acid-Base Titration

A

A basic (or acidic) solution of unknown concentration is reacted with an acidic (or basic) solution of known concentration, in order to determine the concentration of the unknown.

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10
Q

Equivalence Point

A

The point in a titration at which the added solute completely reacts with the solute present in the solution; for
acid–base titrations, the point at which the amount of acid is stoichiometrically equal to the amount of base in solution.

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11
Q

Titration of a Strong Acid with a Strong Base

A
  • The initial pH is simply the pH of the strong acid solution to be titrated.
  • Before the equivalence point, H3O+is in excess. Calculate the [H3O+] by subtracting the number of moles of added OH-from the initial number of moles of H3O+ and dividing by the total volume.
  • At the equivalence point, neither reactant is in excess and the pH=7.00.
  • Beyond the equivalence point, OH- is in excess. Calculate the [OH-] by subtracting the initial number of moles of H3O+ from the number of moles of added OH- and dividing by the total volume.
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12
Q

Titration of a Weak Acid with a Strong Base

A
  • The initial pH is that of the weak acid solution to be titrated. Calculate the pH by working an equilibrium problem using the concentration of the weak acid as the initial concentration.
  • Between the initial pH and the equivalence point, the solution becomes a buffer. Use the reaction stoichiometry to calculate the amounts of each buffer component and then use the Henderson–Hasselbalch equation to calculate the pH.
  • Halfway to the equivalence point, the buffer components are exactly equal and pH = pKa.
  • At the equivalence point, the acid has all been converted into its conjugate base. Calculate the pH by working an equilibrium problem for the ionization of water by the ion acting as a weak base . (Calculate the concentration
    of the ion acting as a weak base by dividing the number of moles of the ion by the total volume at the equivalence point.)
  • Beyond the equivalence point, OH- is in excess. Ignore the weak base and calculate the [OH-] by subtracting the initial number of moles of H3O+ from the number of moles of added OH- and dividing by the total volume.
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13
Q

Solubility Product Constant (Ksp)

A
  • Represents the dissolution of a slightly to moderately soluble ionic compound.
  • Example:

Ksp = [Ca2+][F-]2

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14
Q

Molar Solubility

A

The solubility of a compound in units of mol/L

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15
Q

Solubility of an Ionic Compound

A
  • Lower in a solution containing a common ion than in pure water.
  • With a strongly basic or weakly basic anion the solubility increases with increasing acidity (decreasing pH).
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16
Q

Q < Ksp

A
  • The solution is unsaturated.
  • More of the solid ionic compound can dissolve in the solution.
17
Q

Q = Ksp

A
  • Solution is saturated.
  • Additional solid will not dissolve in the solution.
18
Q

Q > Ksp

A
  • Solution is supersaturated.
  • Excess solid will precipitate out of a supersaturated solution.
19
Q

Selective Precipitation

A

A process involving the addition of a reagant to a solution that forms a precipitate with one of the dissolved ions but not the others.

20
Q

Qualitative Analysis

A
  • Way to determine the ions present in an unknown solution
21
Q

Quantitative Analysis

A
  • Concerned with quantity.
  • Way to determine the amounts of substances in a solution or mixture.
22
Q

Complex Ion

A

Contains a central metal ion bound to one or more ligands.

23
Q

Ligand

A

A neutral molecule or ion that acts as a Lewis base with the central metal ion.

24
Q

Formation Constant, Kf

A

Kf = [products] / [reactants]

  • Equilibrium constant for the formation of a complex ion.
25
Q

Molar Solubility

A

The number of moles of salt dissolved in one liter of its saturated solution.