The Equilibrium Constant (): This value represents the ratio of the mathematical product of the concentrations (or pressures) of the reaction products to those of the reactants, each raised to the power of their stoichiometric coefficients.
vs. : Calculations are typically performed using molarity () for aqueous or gaseous systems, denoted as , or using partial pressures for gaseous systems, denoted as .
The Law of Mass Action: For a general reversible reaction , the equilibrium expression is defined as , where square brackets denote equilibrium concentrations.
Exclusion of Pure Phases: Pure solids () and pure liquids () are excluded from the equilibrium expression because their effective concentrations (activities) remain constant throughout the reaction.
Initial (I): The first step involves listing the starting concentrations or pressures of all species before the reaction begins, often with products starting at zero.
Change (C): This row tracks the shift toward equilibrium using a variable , where the change for each species is proportional to its stoichiometric coefficient (e.g., for a reactant with a coefficient of 2).
Equilibrium (E): The final row represents the sum of the Initial and Change rows (), providing the algebraic expressions used in the equilibrium constant formula.
Solving for : Once the equilibrium expressions are substituted into the formula, algebraic methods (such as the quadratic formula or approximations for very small values) are used to find the value of .
Partial Pressure Fundamentals: In a mixture of gases, the partial pressure of an individual gas is the pressure it would exert if it occupied the container alone.
Mole Fraction Approach: Partial pressure () can be calculated by multiplying the mole fraction of the gas (moles of gas divided by total moles) by the total pressure of the system ().
Expression: Similar to , the expression uses partial pressures: .
Units of : The units for depend on the difference in the number of moles of gaseous products and reactants, typically expressed in , , or raised to the appropriate power.
The Reaction Quotient (): is calculated using the same formula as , but with concentrations or pressures measured at any specific moment in time, not necessarily at equilibrium.
Predicting Direction: Comparing to determines which way the reaction will shift to reach equilibrium.
| Condition | Meaning | Direction of Shift |
|---|---|---|
| Too many reactants | Shift Right (Forward) | |
| Too many products | Shift Left (Reverse) | |
| System at Equilibrium | No Net Change |
Verify the Balanced Equation: Always ensure the chemical equation is balanced before writing the expression, as coefficients directly become exponents.
Check the Phase Labels: Be vigilant for and symbols; including these in your calculation is a frequent source of error.
Volume Consistency: When given moles and volume, always convert to concentration () before substituting into the expression, unless the volume terms cancel out.
Significant Figures: Match the precision of your final value to the least precise measurement provided in the problem (usually 2 or 3 significant figures).