Chemistry Part I - Class XII Complete Comprehensive XII Study Guide

  • Types of Solutions
    • Solutions are homogeneous mixtures of two or more components.
    • Binary solutions consist of two components: Solvent (component in largest quantity) and Solute.
    • Gaseous solutions: Air (Gas in Gas), Chloroform in Nitrogen (Liquid in Gas).
    • Liquid solutions: Glucose in Water (Solid in Liquid), Ethanol in Water (Liquid in Liquid), Oxygen in Water (Gas in Liquid).
    • Solid solutions: Alloys like Gold and Copper (Solid in Solid), Solution of hydrogen in palladium (Gas in Solid).
  • Expressing Concentration
    • Mass percentage (w/ww/w):
      Mass % of component=Mass of component in solutionTotal mass of solution×100\text{Mass } \% \text{ of component} = \frac{\text{Mass of component in solution}}{\text{Total mass of solution}} \times 100
    • Volume percentage (v/vv/v):
      Volume % of component=Volume of componentTotal volume of solution×100\text{Volume } \% \text{ of component} = \frac{\text{Volume of component}}{\text{Total volume of solution}} \times 100
    • Molarity (MM):
      M=Moles of soluteVolume of solution in dm3M = \frac{\text{Moles of solute}}{\text{Volume of solution in } dm^3}
    • Molality (mm):
      m=Moles of soluteMass of solvent in kgm = \frac{\text{Moles of solute}}{\text{Mass of solvent in kg}}
    • Mole Fraction (xx):
      x<em>i=n</em>injx<em>i = \frac{n</em>i}{\sum n_j} (Sum of all mole fractions is 1).
    • Parts per million (ppmppm): Used for very dilute solute concentrations.
  • Solubility
    • Max amount of solute that can be dissolved in a specific amount of solvent at a given temperature.
    • Solubility of Liquid in Liquid/Solid in Liquid: Follows "like dissolves like" (Polar solutes in polar solvents).
    • Solubility of Gas in Liquid: Increases with pressure.
    • Henry's Law: The partial pressure of the gas in vapor phase (pp) is proportional to the mole fraction of the gas (xx) in the solution: p=KHxp = K_H x.
    • Higher KHK_H means lower solubility at a given pressure.
    • Solubility of gases decreases with increase in temperature.
  • Vapor Pressure and Raoult's Law
    • Raoult's Law: In a solution of volatile liquids, the partial vapor pressure of each component is directly proportional to its mole fraction: p<em>i=p</em>i0xip<em>i = p</em>i^0 x_i.
    • Total pressure P<em>total=p</em>10x<em>1+p</em>20x2P<em>{total} = p</em>1^0 x<em>1 + p</em>2^0 x_2.
    • Ideal Solutions: Obey Raoult’s law over the entire concentration range. ΔH<em>mix=0\Delta H<em>{mix} = 0 and ΔV</em>mix=0\Delta V</em>{mix} = 0.
    • Non-Ideal Solutions: Show deviations from Raoult's law.
    • Positive deviation: ABA-B interactions weaker than AAA-A or BBB-B.
    • Negative deviation: ABA-B interactions stronger than AAA-A or BBB-B.
    • Azeotropes: Binary mixtures having the same composition in liquid and vapor phase and boil at a constant temperature.
  • Colligative Properties
    • Properties that depend only on the number of solute particles, not their nature.
    • Relative Lowering of Vapor Pressure:
      p<em>10p</em>1p<em>10=x</em>2w<em>2×M</em>1M<em>2×w</em>1\frac{p<em>1^0 - p</em>1}{p<em>1^0} = x</em>2 \approx \frac{w<em>2 \times M</em>1}{M<em>2 \times w</em>1}
    • Elevation of Boiling Point:
      ΔT<em>b=T</em>bT<em>b0=K</em>bm\Delta T<em>b = T</em>b - T<em>b^0 = K</em>b m
    • Depression of Freezing Point:
      ΔT<em>f=T</em>f0T<em>f=K</em>fm\Delta T<em>f = T</em>f^0 - T<em>f = K</em>f m
    • Osmotic Pressure:
      π=CRT=n2VRT\pi = CRT = \frac{n_2}{V} RT
    • Van't Hoff Factor (ii)
    • Accounts for association or dissociation of solute.
    • i=Normal molar massAbnormal molar mass=Observed colligative propertyCalculated colligative propertyi = \frac{\text{Normal molar mass}}{\text{Abnormal molar mass}} = \frac{\text{Observed colligative property}}{\text{Calculated colligative property}}
    • Updated formulas: ΔT<em>b=iK</em>bm\Delta T<em>b = i K</em>b m, π=iCRT\pi = i CRT.