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Weak Bases
Bases that do not completely ionize.
Monoprotic Acids
Acids that have only one acidic proton.
Polyprotic Acids
Acids with more than one acidic proton.
Ka
Acid dissociation constant, a measure of acid strength.
Kb
Base dissociation constant, a measure of base strength.
pKa
The negative base-10 logarithm of the acid dissociation constant (Ka).
pKb
The negative base-10 logarithm of the base dissociation constant (Kb).
pH
The negative base-10 logarithm of the hydronium ion concentration [H3O+].
pOH
The negative base-10 logarithm of the hydroxide ion concentration [OH-].
Kw
The ion product constant for water.
pKw
Equals pKa + pKb = 14.
Oxyacids
Oxygen containing acid.
pH
A measure of the concentration of hydrogen ions in a solution; calculated as the negative logarithm of [H+].
pH Formula
pH = -log[H+]
pOH
A measure of the concentration of hydroxide ions in a solution; calculated as the negative logarithm of [OH-].
pOH Formula
pOH = -log[OH-]
pH and pOH Relationship
pH + pOH = 14
Strong Acid
An acid that completely dissociates into ions in solution.
Strong Base
A base that completely dissociates into ions in solution.
Weak Acid
An acid that only partially dissociates into ions in solution.
Ka
The equilibrium constant for the dissociation of a weak acid.
Kb
The equilibrium constant for the dissociation of a weak base.
Relationship Between Ka, Kb, and Kw
Kw = Ka * Kb
Approximation Method
Used to simplify calculations for weak acids and bases, assuming that the change in initial concentration is small.
Validity of Approximation Rule
If the initial concentration of the acid or base is 1000 times greater than Ka or Kb, the approximation is valid.
5% Rule
If the change in concentration is less than 5% of the initial concentration, the approximation is valid.
Polyprotic Acid
An acid with multiple ionizable protons.
Oxalic Acid
A polyprotic acid with two ionization constants, Ka1 and Ka2.
Common Ion Effect
The shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved substance.
Buffer
A solution that resists changes in pH upon the addition of small amounts of acid or base.
pH Buffer
Resists change to added H+ or OH-.
Henderson-Hasselbalch Equation
pH = pKa + log ([A-]/[HA]), where [A-] is the concentration of the conjugate base and [HA] is the concentration of the weak acid.
pKa
pKa = -log(Ka), where Ka is the acid dissociation constant.
Aqueous Equilibria
Deals with buffers, titrations, and solubility (Ksp).
Buffer Solutions
Solutions that resist changes in pH upon addition of small amounts of acid or base.
Titration
An analytical technique used to determine the concentration of an unknown solution by neutralizing it with a solution of known concentration (titrant).
Analyte
The substance being analyzed in a titration.
Endpoint
The point at which the titration has ended, ideally coinciding with the equivalence point.
Equivalence Point (Eq. Pt.)
The point in a titration where the amount of titrant added is chemically equivalent to the amount of analyte in the sample.
Acid/Base Titration
A type of titration involving reactions between acids and bases.
Titrations of Polyprotic Acids
Titration involving acids that can donate more than one proton.
Solubility Product (Ksp)
The equilibrium constant representing the solubility of a sparingly soluble salt.
Solubility Product (Ksp)
The equilibrium constant for the dissolution of a solid substance into an aqueous solution.
LD50
The amount of a chemical that is lethal to 50% of the experimental animals exposed.
Common Ion Effect
The decrease in solubility of an ionic precipitate by the addition of a different ionic compound that contains the same ion as found in the ionic precipitate; a consequence of Le Chatelier's Principle.
Barium Sulfate (BaSO4)
An insoluble compound of barium; used as an absorber and shows white on X-rays to help in GI tract investigations.
Molar Solubility (s)
The solubility of a compound expressed in moles per liter (mol/L).