Equilibrium and Solution EquilibriumThis is a featured page

Equilibrium-
  • reactions can go in both directions:
    • R --> P
    • R <-- P
  • when the rate of the forward reaction is equal to the rate of the reverse reaction (rate of R --> P = rate of R <-- P)
  • no net change is observed

5 Flavas of K ~
  1. K / Keq / Kc = standard K; concentrations are typically in molarities
  2. Kp = for gasses; values used to calculate are partial pressures, not concentrations
  3. Ksp = solubility product constant; uses molarities of slightly soluble compounds in aqueous solutions
  4. Ka = weak acids (HAVEN'T LEARNED YET)
  5. Kb = weak bases (HAVEN'T LEARNED YET)

Equilibrium constant = K
- For the general reaction a A + b B <--> c C + d D (italics are coefficients),
K = [C]^c[D]^d
[A]^a[B]^b also known as the equilibrium constant expression.
- If K>1, reaction is product-favored
- If K<1, reaction is reactant-favored

Equilibrium constant expression
- All concentrations at equilibrium values
- Product concentrations in numerator; reactant concentrations in denominator
- Concentration is raised to power of stoichiometric coefficient (from equation)
- K depends on reaction and temperature
- K has no units
- Concentrations of solid reactants/products are not included
- Concentration of (liquid) water is not included

Rules for Writing Kc Expressions:
-Kc is a function of temperature
-Do not put solids or pure liquids in the Kc expression
-Kc Reverse = 1/ Kc forward
-If you multiply the chemical equation by n, then you raise Kc to n
-If you add chemical reactions to get a final reaction, multiply the Kc's expression to get the final reaction Kc

Reaction Quotient = Q
- For the general reaction a A + b B <--> c C + d D (italics are coefficients),
Q = [C]^c[D]^d
[A]^a[B]^b
- At equilibrium, Q = K
- When Q<K, reactants --> products
- When Q>K, reactants <-- products

Dalton's Law of Partial Pressures
the total pressure of a gas system = the sum of the individual pressures
Pt = Pa + Pb + Pc . . .
Pt V = Nt RT
Kp = Kc * (RT) ^ delta N
R = universal gas constant, T = temperature, delta N = moles of gas product - moles of gas reactant

Ksp solubility product constant
How much of a slightly soluble substance dissolves at a certain temperature
Solubility doesn't equal product constant

Solubility- How much of the solid or an ion is dissolved at a given temperature
- in the units of Molarity (mol/L) or g/L or g/mL
- Ksp cannot be compared directly unless they have EQUAL ion ratios

Solubility tells you how much of a solid can dissolved before the solution is saturated
-anything more than the solubility will precipitate out.
-any amount under solubility is unsaturated.
-supersaturated is a special case where the solution is holding more than it normally holds at that temperature. When it is disrupted, any amount over the solubilities will precipitate out.

Q< Ksp unsaturated (more will dissolve)
Q= Ksp saturated (no more will dissolve; any more will precipitate out)
Q> Ksp supersaturated(excess will precipitate out until Q=Ksp)

<-------------------------
COMMON ION EFFECT
AgI <--> Ag+ + I-
NaI

pH Rules
pH = -log[H+]
[H+] = 1 x 10^(-pH)
[H+][OH-] = 1 x 10^-14
pOH = - log [OH-]
pH + pOH = 14
Temperature is the only disturbance (that we have learned) that changes K.
The following are trixies of Le Chat's that have no effect on K:
-adding a catalyst
-adding a pure solid of liquid
-adding an inert

Le Chatelier's Principle
DisturbanceChange as Mixture Returns to EquilibriumEffect on EquilibriumEffect on K
Addition of ReactantReactants Consumed
Products Formed
Shift RightNo Effect
Addition of ProductProducts Consumed , Reactants FormedShift LeftNo Effect
Increase TemperatureHeat Energy Consumed by SystemExo shift left
Endo shift right
K will change
Decrease in TemperatureHeat Energy ReleasedEndo shift left
Exo shift right
K will change
V down P upShift to Relieve PressureShift to side of fewer moles of gasNo Effect
V up P downShift to Make PressureShift to more moles of gasNo Effect
Add catalyst, Add Pure Solid or Liquid,
add Inert Gas

No EffectNo Effect



claire.lee
claire.lee
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