Molality to Molarity, Colligative Properties, and Colloids - Study Notes
Molality to Molarity: Conversion and Applications
- Definition of molality
- m=m</em>extsolventn<em>extsolite where $m$ is in mol/kg (molality) and $n{ ext{solute}}$ is the number of moles of solute, $m{ ext{solvent}}$ is the mass of the solvent in kilograms.
- The lecture fixes the solvent mass to 1 kg to make molality directly equal to the number of moles of solute, i.e., $m = n{ ext{solute}}$ when $m{ ext{solvent}} = 1 ext{ kg}$.
- General steps to convert molality to molarity
- Determine the number of moles of solute: n<em>extsolute=M<em>extsolutem</em>extsolute where $M{ ext{solute}}$ is the molar mass of the solute.
- Compute the mass of the solute: m<em>extsolute=n</em>extsoluteimesMextsolute.
- Determine the mass of the solution: m<em>extsolution=m</em>extsolute+mextsolvent.
- Convert to volume using density: V{ ext{solution}} = rac{m{ ext{solution}}}{
ho{ ext{solution}}} where $
ho{ ext{solution}}$ is in g/mL; convert to liters for molarity. - Compute molarity: M=V</em>extsolutionn<em>extsolute
- Worked example (glucose in water)
- Given: molality $m = 0.11$ m, solute glucose, MW $M{ ext{glucose}} = 180.2 ext{ g/mol}$, solvent mass $m{ ext{solvent}} = 1.000 ext{ kg}$.
- Number of moles of glucose: nextglucose=mimes1extkg=0.11extmol.
- Mass of glucose: m<em>extglucose=n</em>extglucoseimesMextglucose=0.11imes180.2=19.82extg.
- Mass of solution: mextsolution=1000extg+19.82extg=1019.82extg.
- Density (solution) used: $
ho_{ ext{solution}}
ightarrow 1.064 ext{ g/mL}$ (approx at these conditions). - Volume of solution: Vextsolution=1.0641019.82extmL o958.5extmL=0.9585extL.
- Molarity: M=V</em>extsolutionn<em>extglucose=0.95850.11 o0.1148extM.
- Key concepts: electrolytes, nonelectrolytes, and the role of particle count
- Electrolytes ionize in solution and conduct electricity; nonelectrolytes do not ionize (e.g., glucose).
- Colligative properties depend on the number of dissolved particles, not their identity.
- Van't Hoff factor $i$ accounts for the effective number of particles formed by dissolution: for nonelectrolytes, $i=1$; for electrolytes, $i>1$ (depending on dissociation).
- Vapor pressure lowering (Raoult’s law form)
- Vapor pressure of the solution: P<em>extsolution=P0(1−x</em>extsolute) where $P^{0}$ is the vapor pressure of the pure solvent, and $x_{ ext{solute}}$ is the mole fraction of the solute.
- Alternative algebraic form: P<em>extsolution=P0−x</em>extsoluteP0extor(P0−P<em>extsolution)=x</em>extsoluteP0.
- Mole fraction of solute: x<em>extsolute=n<em>extsolute+n</em>extsolventn</em>extsolute.
- This framework yields the change in vapor pressure, $ riangle P = P^{0} - P{ ext{solution}} = x{ ext{solute}} P^{0}$, which is positive (i.e., $P_{ ext{solution}}$ is lower than $P^{0}$).
- Example: 73.56 g sucrose in 1 L of solution at 100°C
- $n_{ ext{sucrose}} = rac{73.56}{342.30} approx 0.2149 ext{ mol}$.
- Density of solution at 100°C: $
ho{ ext{solution}} = 0.9957 ext{ g/mL}$ → mass of 1 L solution: $m{ ext{solution}} = 995.7 ext{ g}$. - Mass of water (solvent): $m_{ ext{water}} = 995.7 - 73.56 = 922.14 ext{ g}$.
- Moles water: $n_{ ext{water}} = rac{922.14}{18.015} approx 51.17 ext{ mol}$.
- Mole fraction of sucrose: x_{ ext{sucrose}} = rac{0.2149}{0.2149 + 51.17} approx 0.00418.
- Vapor pressure of solution: $oxed{P{ ext{solution}} = P^{0}(1 - x{ ext{sucrose}}) = 760 ext{ mmHg}(1 - 0.00418) approx 756.8 ext{ mmHg}}$.
- Vapor pressure lowering: $ riangle P = x_{ ext{sucrose}} P^{0} approx 3.18 ext{ mmHg}$.
- Boiling point elevation (BP elevation)
- Definition: riangleT<em>b=iK</em>bm where $K_b$ is the ebullioscopic constant and $m$ is molality.
- For a nonelectrolyte, $i = 1$; for water, $K_b = 0.5652 ext{ °C} ext{ kg/mol}$.
- Using the example molality $m approx 0.2331 ext{ m}$ (from the glucose example),
- riangle T_b approx 1 imes 0.5652 imes 0.2331 approx 0.132 ext{ °C}.
- Thus, $T_{ ext{solution}} approx 100.0 ext{ °C} + 0.132 ext{ °C} approx 100.13 ext{ °C}$.
- Freezing point depression
- Definition: riangleT<em>f=iK</em>fm where $K_f$ is the cryoscopic constant.
- For water, $K_f = 1.86 ext{ °C kg/mol}$; for nonelectrolyte, $i = 1$.
- With $m approx 0.2331 ext{ m}$,
- riangle T_f approx 1.86 imes 0.2331 approx 0.433 ext{ °C}.
- Freezing point of solution: $T_f( ext{solution}) = 0.0 ext{ °C} - 0.433 ext{ °C} approx -0.433 ext{ °C}.$
- Ion effects and the Van't Hoff factor
- For ionic compounds, the solute particles increase due to dissociation; the effective number of particles is given by the Van't Hoff factor $i$.
- Examples:
- NaCl → Na⁺ + Cl⁻, so $i approx 2$.
- CaCl₂ → Ca^{2+} + 2 Cl⁻, so $i approx 3$.
- When calculating colligative properties for ionic solutes, use $ riangle T = i K m$ (or $P_{ ext{solution}}$ via mole fractions with the effective particle count).
- Ionic equation reminder: NaCl(s)
ightarrow Na^{+} + Cl^{-}; CaCl_{2}(s)
ightarrow Ca^{2+} + 2 Cl^{-}.
- Quick practical example: 0.05 m CaCl₂
- $i = 3$ (three particles: Ca^{2+} and 2 Cl⁻).
- $ riangle Tf = i Kf m = 3 imes 1.86 imes 0.05 approx 0.279^ ext{°C}$.
- $T_f( ext{solution}) approx 0.0^ ext{°C} - 0.279^ ext{°C} approx -0.279^ ext{°C}$.
- Molecular weight determination via freezing point depression
- Given a mass of solute that lowers the freezing point of a solvent by a measured amount, you can back-calculate the molecular weight of the solute.
- For a nonelectrolyte: compute molality from the depression, then find moles from solvent mass, and finally MW = mass_solute / n.
- Example: 13.6 g unknown non-electrolyte lowers freezing point of benzene by $ riangle Tf = 0.540^ ext{°C}$; $Kf( ext{benzene}) = 5.12^ ext{°C kg/mol}$; solvent mass $m_{ ext{solvent}} = 2.50 ext{ kg}$.
- m = rac{ riangle Tf}{Kf} = rac{0.540}{5.12} approx 0.1055 ext{ mol/kg}.
- n = m imes m_{ ext{solvent}} = 0.1055 imes 2.50 approx 0.2638 ext{ mol}.
- MW = rac{m_{ ext{sample}}}{n} = rac{13.6}{0.2638} approx 51.6 ext{ g/mol}.$
- Additional notes on density and units
- Always track density units to convert mass to volume properly: e.g., $
ho{ ext{solution}} = 0.9957 ext{ g/mL}$ implies $m{ ext{solution}} =
ho{ ext{solution}} imes V{ ext{solution}}$ with $V$ in mL. - Sign conventions: boiling point elevation yields a positive $ riangle T_b$; freezing point depression yields a negative freezing point for the solution relative to the pure solvent.
- When applying equations, check that the final temperatures make sense with the physical meaning (e.g., $T{ ext{solution}} > T{ ext{pure}}$ for BP elevation).
- Quick recap: key formulas to memorize
- Molality: m=m</em>extsolventn<em>extsolute
- Molarity: M=V</em>extsolutionn<em>extsolute
- Number of moles: n<em>extsolute=Mextsolutem</em>extsolute
- Mass of solution: m<em>extsolution=m</em>extsolute+mextsolvent
- Volume from density: V{ ext{solution}} = rac{m{ ext{solution}}}{
ho_{ ext{solution}}} - Vapor pressure lowering: P<em>extsolution=P0(1−x</em>extsolute)extwithx<em>extsolute=n<em>extsolute+n</em>extsolventn</em>extsolute
- Boiling point elevation: riangleT<em>b=iK</em>bm
- Freezing point depression: riangleT<em>f=iK</em>fm
- For nonelectrolytes: $i = 1$; for electrolytes, adjust $i$ via the number of particles (Van't Hoff factor).
- Molecular weight via freezing point: $MW = rac{m{ ext{solute}}}{n}$ where $n = m imes m{ ext{solvent}}$ and $m = rac{ riangle Tf}{i Kf}$.
- Final practical note
- The same set of concepts applies across problems, just keep track of whether the solute is an electrolyte (affecting $i$) and carefully convert between moles, masses, volumes, and densities.
- The instructor emphasizes practice with signs, unit consistency, and using given constants (e.g., $Kb$, $Kf$, and density) as provided in problems.