A homogeneous mixture of two or more pure substances
Solute
The pure substance present in lesser amounts
Solvent
The more abundant substance
How solutions can be classified
Based on the phase of the solvent
Based on saturation
Based on concentration
Liquid solutions
Solutions where the solvent is a liquid
Solid solutions
Solutions where the solvent is solid
Gaseous solutions
Solutions where the solvent is a gas
Unsaturated solution
The amount of solute is less than the solute's solubility at a given volume and temperature
Saturated solution
The amount of solute is equal to the solute's solubility at a given volume and temperature
Supersaturated solution
The amount of solute is greater than the solute's solubility at a given volume and temperature
Concentrated solution
A solution that contains an excessively large amount of solute
Diluted solution
A solution of low concentration, prepared through the process of dilution
Upon dilution, the concentration of the new solution is lower than the stock solution, but the number of moles remains the same
Liquid-liquid solutions
Carbonated drinks
Liquid-solid solutions
Amalgam (mercury in gold)
An aliquot does not have the same concentration as the stock solution
Based on the phase of the solvent: air
Gaseous solution
Based on concentration: 0.5 M potassium permanganate, KMnO4
Diluted solution
Based on the phase of the solvent: rubbing alcohol
Liquid-liquid solution
Nitric acid fuming: 'by W. Oelen'
Almost all substances dissolve in water under observable temperature and pressure. But some substances do not.
Oil
Forms immiscible bubbles that do not mix with water
Substances that mix easily
Possess "compatible" intermolecular forces of attraction
Explain the effect of temperature on the solubility of a solid and of a gas
STEM_GC11PP-IIId-f-113
Explain the effect of pressure on the solubility of a gas
STEM_GC11PP-IIId-f-114
Intermolecular Forces of Attraction (IMFAs)
Particles of substance exhibit intermolecular forces of attraction and repulsion to one another
London dispersion forces (LDFs)
Exist in all molecules, polar or nonpolar. Strength depends on size, surface area, and polarizability
Ion-ion interactions
Between charged substances. Strength follows Coulomb's law
Dipole-dipole interactions
Between polar, uncharged substances. Strength depends on electronegativity of atoms in a bond
Induced Dipole Interactions
Ions and dipoles induce formation of temporary dipoles on nonpolar molecules
Hydrogen Bonding
Polar molecules that have H atoms bonded to O, N, or F (e.g., H2O, NH3, and HF)
Solution Process
Solute particles must be dissolved in solvent particles. A change in IMFAs between the particles: solvent-solvent interaction, solute-solute interaction, solute-solvent interaction
Molar enthalpies
Energy changes that accompany each of the interactions
Heat of Solution, ΔHmixing
Also referred to as ΔHsoln. Sum of all the enthalpy changes associated with each step
ΔHmixing = ΔH1 + ΔH2
Is always positive
Sign of ΔHmixing
Depends on the magnitudes of the three enthalpy changes
ΔHmixing > 0
Is endothermic. ΔH1 + ΔH2 is greater than ΔH3. Solvent-solvent and solute-solute interactions are stronger than solute-solvent interactions
ΔHmixing < 0
Is exothermic. ΔH1 + ΔH2 is less than ΔH3. Solvent-solvent and solute-solute interactions are weaker than solute-solvent interactions
Entropy (ΔS)
The inherent tendency toward disorder in highly favorable processes. The chaos when solute and solvent particles mix in comparison to their initial ordered states
Solubility
The extent to which a solute dissolves in solvent at a particular temperature, governed by both ΔHmixing and ΔSmixing