Chemistry: Intermolecular Forces, Solutions, and Chemical Kinetics

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Vocabulary flashcards generated from lecture materials covering intermolecular forces, properties of liquids, solutions and colligative properties, and chemical kinetics.

Last updated 5:06 PM on 9/21/26
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48 Terms

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Intermolecular Forces

Attractions and repulsions between neighboring particles (atoms, molecules, or ions) that hold solids and liquids together, distinct from intramolecular chemical bonds.

<p>Attractions and repulsions between neighboring particles (atoms, molecules, or ions) that hold solids and liquids together, distinct from intramolecular chemical bonds.</p>
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Intramolecular Forces

Chemical bonding forces (such as ionic and covalent bonds) within a molecule that govern molecular stability and chemical properties.

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Ion-Dipole Forces

Intermolecular electrostatic interactions occurring between an ion and the partial charges of a permanent dipole on a polar molecule, with strengths typically ranging from 1050 kJ/mol10\text{--}50\text{ kJ/mol}.

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Dipole-Dipole Forces

Intermolecular attractions resulting from electrical interactions between permanent dipoles on adjacent polar molecules, with strengths typically ranging from 34 kJ/mol3\text{--}4\text{ kJ/mol}.

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London Dispersion Forces

Weak intermolecular forces (110 kJ/mol1\text{--}10\text{ kJ/mol}) present between all particles, caused by temporary fluctuations in electron density that induce temporary dipoles in adjacent molecules.

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Polarizability

The measure of the ease with which the electron cloud of an atom or molecule can be distorted by an external electrical charge or neighboring dipole.

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Hydrogen Bond

A moderate attractive force (1040 kJ/mol10\text{--}40\text{ kJ/mol}) between a hydrogen atom bonded to a highly electronegative atom (N\text{N}, O\text{O}, or F\text{F}) and a lone pair on a neighboring electronegative atom.

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Viscosity

The quantitative measure of a liquid's internal resistance to flow.

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Surface Tension

The energy required to increase the surface area of a liquid, caused by the unbalanced inward attractive forces experienced by surface molecules.

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Equilibrium Vapor Pressure

The pressure exerted by a vapor in dynamic equilibrium with its liquid phase in a closed container at a given temperature, where rate of evaporation equals rate of condensation.

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Critical Point

The specific combination of critical temperature and critical pressure beyond which distinct liquid and gas phases cease to exist.

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Critical Temperature

The temperature above which a gas cannot be liquefied, regardless of the magnitude of the applied pressure.

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Supercritical Fluid

A high-density state of matter formed beyond the critical point that exhibits properties of both liquids and gases.

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Triple Point

The unique condition of temperature and pressure at which solid, liquid, and gas phases of a substance coexist in dynamic equilibrium.

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Enthalpy of Fusion (ΔHfusion\Delta H_{\text{fusion}})

The amount of energy required to convert a given quantity of a solid into its liquid state at its melting point.

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Enthalpy of Vaporization (ΔHvap\Delta H_{\text{vap}})

The amount of energy required to convert a given quantity of a liquid into its gaseous state at its boiling point.

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Clausius-Clapeyron Equation

An equation expressing the logarithmic relationship between the vapor pressure of a liquid and temperature: ln(Pvap)=ΔvapHRT+C\ln(P_{\text{vap}}) = -\frac{\Delta_{\text{vap}}H^\circ}{RT} + C.

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Solution

A homogeneous mixture composed of two or more substances single-phased throughout.

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Solvent

The component of a solution present in the largest quantitative amount.

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Solute

The minor component dissolved within a solvent to form a solution.

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Molarity (MM)

A concentration unit defined as the number of moles of solute dissolved per liter of solution (mol/L\text{mol/L}).

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Molality (mm)

A temperature-independent concentration unit defined as the number of moles of solute per kilogram of solvent (mol/kg\text{mol/kg}).

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Mole Fraction (XX)

A dimensionless concentration expression defined as the ratio of moles of a specific component to the total moles of all components in a solution.

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Parts Per Million (ppm)

A concentration measure calculated as mass of solutemass of solution×106\frac{\text{mass of solute}}{\text{mass of solution}} \times 10^6.

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Saturated Solution

A solution that contains the maximum concentration of dissolved solute in dynamic equilibrium with undissolved solute.

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Supersaturated Solution

An unstable solution containing a greater amount of dissolved solute than present at thermodynamic equilibrium.

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Henry's Law

A relationship stating that the solubility of a gas in a liquid is directly proportional to the partial pressure of that gas above the liquid (Solubility=k×P\text{Solubility} = k \times P).

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Colligative Properties

Physical properties of solutions that depend solely on the total concentration of solute particles, regardless of their chemical identity.

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Raoult's Law

A principle stating that the partial vapor pressure of a solvent above a solution is equal to the vapor pressure of pure solvent multiplied by its mole fraction: Psoln=Psolv×XsolvP_{\text{soln}} = P_{\text{solv}} \times X_{\text{solv}}.

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van 't Hoff Factor (ii)

The ratio of moles of dissolved particles in solution to moles of solute formula units initially dissolved.

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Osmosis

The spontaneous net passage of solvent molecules through a semipermeable membrane from a solution of lower solute concentration to one of higher solute concentration.

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Osmotic Pressure (Π\Pi)

The pressure required to stop osmotic solvent flow across a semipermeable membrane, given by Π=iMRT\Pi = iMRT.

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Chemical Kinetics

The area of chemistry concerned with measuring reaction rates and elucidating the sequence of elementary steps in reaction mechanisms.

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Reaction Rate

The positive change in product concentration per unit time or the negative change in reactant concentration per unit time.

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Rate Law

An experimentally determined equation relating the rate of a chemical reaction to the rate constant (kk) and reactant concentrations raised to specific powers.

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Rate Constant (kk)

A temperature-dependent proportionality constant in the rate law expression specific to a given reaction.

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Half-Life (t1/2t_{1/2})

The time period required for the concentration of a reactant to decrease to exactly one-half of its initial value.

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Reaction Mechanism

The step-by-step sequence of individual elementary reactions that describes the precise molecular path from reactants to products.

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Elementary Reaction

A single, discrete step in a reaction mechanism that describes an individual molecular collision or event.

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Reactive Intermediate

A chemical species produced in an early elementary step of a mechanism and consumed in a subsequent step, not appearing in the overall balanced equation.

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Molecularity

The total number of reactant molecules, atoms, or ions coming together in a single elementary reaction step.

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Rate-Determining Step

The slowest elementary step in a reaction mechanism, which acts as a bottleneck and dictates the overall reaction rate law.

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Activation Energy (EaE_a)

The minimum threshold energy colliding reactant molecules must possess for a reaction to occur.

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Transition State

The transient, high-energy arrangement of atoms formed at the peak of the potential energy barrier during a chemical reaction, also called the activated complex.

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Arrhenius Equation

An equation expressing the mathematical dependence of the rate constant on temperature and activation energy: k=AeEa/RTk = A e^{-E_a/RT}.

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Catalyst

A substance that accelerates a chemical reaction by offering an alternative pathway with lower activation energy without being permanently consumed.

<p>A substance that accelerates a chemical reaction by offering an alternative pathway with lower activation energy without being permanently consumed.</p>
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Homogeneous Catalyst

A catalyst present in the same physical phase as the reacting species.

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Heterogeneous Catalyst

A catalyst present in a different physical phase from the reacting species, typically a solid catalyst in a liquid or gaseous reaction mixture.