chapter 14 Colligative Properties, Solution Equilibrium, and Solution Energetics

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Vocabulary flashcards covering colligative properties, solution equilibria, Henry's law, solubility factors, and solution formation energetics from Chemistry lecture notes.

Last updated 2:20 AM on 9/15/26
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23 Terms

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Colligative property

A property of a solution that depends on the number of particles dissolved in the solution, not the type of particle.

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Vapor pressure lowering

A colligative property where the vapor pressure of a solution is lower than the vapor pressure of the pure solvent.

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Vapor pressure lowering equation

The mathematical relationship expressed as Psolution=XsolventPsolventoP_{\text{solution}} = X_{\text{solvent}} P^\text{o}_{\text{solvent}}.

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Freezing point depression

A colligative property where the freezing point of a solution is lower than the freezing point of the pure solvent.

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Boiling point elevation

A colligative property where the boiling point of a solution is higher than the boiling point of the pure solvent.

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Strong electrolyte solutions in colligative properties

Solutions that produce more colligative properties than non-electrolyte solutions because they dissociate into a greater number of particles.

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Solubility

The amount of a substance that dissolves in a given amount of solvent.

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Saturated solution

A solution in which the dissolved solute is in dynamic equilibrium with the solid (undissolved) solute; the amount of dissolved solute equals the solubility, so added solute will not dissolve.

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Unsaturated solution

A solution containing less than the equilibrium amount of solute; if additional solute is added, it will dissolve.

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Supersaturated solution

An unstable solution containing more than the equilibrium amount of solute, which will normally precipitate out of the solution.

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Solubility of NaCl in water

Equals 35 g/100 g35\text{ g}/100\text{ g} water at 25 oC25\text{ }^\text{o}\text{C}; if added beyond 35 g35\text{ g}, the excess will stay solid and will not dissolve.

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Henry's law

A law quantifying gas solubility with increasing pressure using the equation Sgas=kHPgasS_{\text{gas}} = k_H P_{\text{gas}}, showing solubility is directly proportional to partial pressure.

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SgasS_{\text{gas}}

The solubility of a gas in Henry's law, usually expressed in units of molarity (MM).

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kHk_H

The constant of proportionality in Henry's law, called the Henry's law constant.

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PgasP_{\text{gas}}

The partial pressure of a gas above a liquid in Henry's law, usually expressed in atmospheres (atm\text{atm}).

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Temperature effect on solid and liquid solubility

The general trend where solubility of solids and liquids increases with an increase in temperature.

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Temperature effect on gas solubility

The trend where solubility of gases in liquids decreases with increasing temperature.

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Exothermic solution process (aHsolute<aHhydration|\text{a}H_{\text{solute}}| < |\text{a}H_{\text{hydration}}|)

A process where releasing energy when water wraps around ions gives off more heat than it takes to pull solute apart, releasing extra heat (aH<0\text{a}H < 0) and making the solution feel warm.

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Endothermic solution process (aHsolute>aHhydration|\text{a}H_{\text{solute}}| > |\text{a}H_{\text{hydration}}|)

A process where pulling solute apart takes more energy than water gives back, stealing heat from surroundings (aH>0\text{a}H > 0) and making the solution feel cold.

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Enthalpy of solution (aHsoln\text{a}H_{\text{soln}})

According to Hess's law, the overall enthalpy change upon solution formation given by aHsoln=aHsolute+aHsolvent+aHmix\text{a}H_{\text{soln}} = \text{a}H_{\text{solute}} + \text{a}H_{\text{solvent}} + \text{a}H_{\text{mix}}.

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aHsolute\text{a}H_{\text{solute}}

The positive (endothermic) energy required to break apart the solute particles.

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aHmix\text{a}H_{\text{mix}}

The exothermic step (aHmix<0\text{a}H_{\text{mix}} < 0) where energy is released as solute particles interact with solvent particles through intermolecular forces.

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Heat of hydration (aHhydration\text{a}H_{\text{hydration}})

The combination of aHsolvent\text{a}H_{\text{solvent}} and aHmix\text{a}H_{\text{mix}} into a single term for aqueous solutions, which is always largest and negative (exothermic) for ionic compounds.