Understanding the behavior of solutions is critical in this course.
Pressure affects solute solubility; lower pressure usually increases solute solubility in solutions.
Concentrated solutions have molecules close together, leading to more interactions.
Less concentrated solutions have molecules further apart, resulting in fewer interactions.
Key values in concentration graphs:
q = 0: Represents a starting point.
q = ∞: Represents a theoretical maximum concentration.
The equation discussed involves activities, which relate to concentrations.
If the concentration of any reactant (C or B) is zero, then q = 0.
If one reactant (A or B) has a concentration of zero, then q = ∞.
Valid q values range anywhere along the line between these extremes, where both reactants are present.
The standard state is often defined in terms of a 1 molar concentration, and this sets our reference point where q = 1.
If q = 0, the Gibbs Free Energy ( \Delta G) equals the standard Gibbs Free Energy of the reaction.
As you move along the graph from q=1, changing the value of q affects the slope, indicating how far the system is from equilibrium.
K is defined similarly to q, representing a specific ratio of products to reactants at equilibrium.
The slope of the q line gives insights into energy levels and distance from equilibrium.
There is only one specific value of q for which energy is minimized, and that is indicated by the equilibrium constant K.
Reactions involving solids (s) or liquids (l) have concentrations for calculations; gases and solutions are considered in terms of their activity.
To calculate \Delta G\ for a reaction:
Product activity values multiplied by their coefficients are summed.
Subtract the reactants' activity values multiplied by their coefficients.
Ensure no zero values are present in calculating \Delta S\ and \Delta H, for which an example results in \Delta S = -199 J/mol.
\Delta G\ is dependent on temperature alongside concentrations and standard conditions.