Chem 1212: Chapters 12-14 – Flashcards
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| Boyle's Law |
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| P1V1=P2V2 |
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| Charles' Law |
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| V1/T1=V2/T2 |
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| Combined Gas Law |
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| P1V1/T1=P2V2/T2 |
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| Avogadro's Law |
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| At the same temperature and pressure, equal volumes of all gases contain the same number of molecules. |
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| Standard Molar Volume |
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| 22.4 L -- One mole of an ideal gas occupies 22.4 L at 0C and 1 atm of pressure. |
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| Ideal Gas Equation |
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| PV=nRT |
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| Dalton's Law of Partial Pressures |
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| The total pressure exerted by a mixture of ideal gases is the sum of the partial pressures of those gases. |
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| Vapor Pressure |
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| Pressure exerted by its gaseous molecules in equilibrium with the liquid. |
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| Kinetic-Molecular Theory |
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| 1. Gases consist of discrete molecules. The individual molecules are very small and far apart relative to their sizes. 2. Gaseous molecules are in continuous, rapid random, straight-line motion with varying velocities. 3. The collisions between gas molecules and with the walls of the container are elastic; the total energy is conserved during a collision. 4. Between collisions, the molecules exert no attractive or repulsive forces on one another; each molecule travels in a straight line with a constant velocity. |
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| Root Mean Square |
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| Urms=sq rt(3RT/Mm) R=8.314 kg m2/s2 K mol Molar mass, Mm, must be in KG/mol |
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| Effusion |
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| Gases exiting through the walls of a container with porous walls. |
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| Diffusion |
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| The movement of a substance into a space or the mixing of one substance with another. |
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| Ratio of Rate of Effusion |
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| R1/R2=sqrt(M2/M1) OR (D2/D1) |
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| Deviations from Ideality |
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| When molecules become close together through increased T or P -- intermolecular forces become important. |
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| Miscible Liquids |
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| Diffuse into each other; they are soluble in each other and form homogeneous solutions. |
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| Intermolecular Forces |
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| Forces between (among) individual particles (atoms, ions, molecules). |
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| Ion-Ion Interactions |
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| Force of attraction between two oppositely charged ions is governed by Coulomb's Law: F=abs(q1q2)/r2 F=magnitude of force r=distance in m q1,q2=charges on bodies (coulombs) |
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| Intermolecular Interaction Strengths |
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| I-I>HB>D-D>>LF |
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| Dipole-Dipole |
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| Occur between the + end of one polar molecule and the - end of the other. |
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| Hydrogen Bonding |
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| Especially strong D-D interaction. Occurs between an H atom in one molecule (attached to an F, O, or N), and an F, O, or N atom in another molecule. |
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| Dispersion Forces (London Forces) |
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| Present in all substances. ONLY kind of interactions for nonpolar substances. Result from the attraction of the nucleus of one atom for the electron cloud of another atom (in a different molecule). They increase with increasing polarizability, the ability of an electron cloud to be distorted. Polarizability increases with increasing numbers of electrons and therefore with increasing sizes of molecules. |
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| Ion-Dipole Interactions |
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| Ion and Dipole. Weaker than Dipole-Dipole. |
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| Change in EN |
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| Nonpolar: 0-0.5 Polar: 0.5-2.0 Ionic: > 2.0 |
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| Viscosity |
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| Resistance to flow. One measure of the forces of attraction within a liquid. Honey = high viscosity; gasoline = low viscosity. |
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| Surface Tension |
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| Measure of the inward forces that must be overcome to expand the surface of a liquid. Molecules on the surface are attracted only toward the interior, while those on the interior are attracted equally in all directions. |
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| Capillary Action |
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| Capillary Rise: Adhesive Forces > Cohesive Forces Capillary Fall: Cohesive Forces > Adhesive Forces |
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| Evaporation |
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| Process by which molecules escape from the surface of a liquid (vaporize). Occurs more rapidly as temperature increases because a greater fraction of molecules possess the necessary escape velocity and kinetic energy. |
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| LeChatelier's Principle |
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| A system at equilibrium, or changing toward equilibrium, responds in the way that tends to relieve or "undo" any stress placed on it. |
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| Vapor Pressure |
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| Pressure exerted by the vapor of the liquid on its surface at equilibrium in a closed container. Because vapor pressures increase as temperature increases, evaporation occurs more rapidly as T increases. |
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| Boiling Point |
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| Temperature at which the vapor pressure of the liquid equals the applied (usually atmospheric) pressure. |
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| Distillation |
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| Process by which a mixture or solution is separated into its components on the basis of differences in BPs of the components. |
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| Specific Heat |
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| Amount of heat required to raise the T of 1g of a substance 1C with no change in state. Q=mC(change in T) |
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| Molar Heat Capacity |
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| Amount of heat required to raise the temperature of 1 mol of a substance 1C with no change in state. Q=mol x molar heat capacity x change in T |
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| Heat of Vaporization |
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| Amount of heat that must be absorbed to convert 1g of a liquid at its BP to a gas with no change in temperature. Usually J/g. |
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| Heat of Condensation |
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| Reverse of Heat of Vaporization. Amount of heat that must be released to liquefy 1g of a gas at its condensation (BP) with no change in T. |
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| Molar Heat of Vaporization |
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| The amount of heat that must be absorbed to convert one mole of a liquid at its BP to a gas with no change in T. |
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| Molar Heat of Condensation |
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| Reverse of molar heat of vaporization. |
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| Melting Point |
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| Temperature at which liquid and solid coexist at equilibrium under a pressure of 1 atm. |
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| Heat of Fusion |
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| The amount of heat required to melt 1g of a solid at its melting point with no change in T. Endothermic. |
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| Heat of Crystallization |
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| Amount of heat liberated by the crystallization of one gram of liquid at its freezing point. Exothermic. |
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| Specific Heat of Water |
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| 4.18 J/gC |
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| Density of Water |
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| 1.00 g/mL |
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| Specific Heat of Ice |
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| 2.09 J/gC |
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| Sublimation |
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| Conversion of a solid directly into vapor. Dry Ice is solid CO2. The white vapors are due to water condensing in the very cold gaseous CO2 near the solid. |
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| Deposition |
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| Vapor directly to solid. |
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| Triple Point |
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| Point at which three phases of a substance can coexist in equilibrium. |
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| Critical Temperature |
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| Temperature above which a gas cannot be liquefied, i.e., the temperature above which the liquid and gas do not exist as distinct phases. |
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| Amorphous Solids |
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| Have no well-defined ordered structure. Waxes, asphalt, and glass. |
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| Critical Pressure |
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| Pressure required to liquefy a gas at its critical temperature. |
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| Critical Point |
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| The combination of critical temperature and critical pressure. |
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| Metallic Solids |
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| Metals. |
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| Ionic Solids |
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| Consist of positive and negative ions arranged in a definite crystal structure. Attractions between oppositely charged ions are strong. |
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| Molecular Solids |
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| Consist of discrete molecules that occupy positions in unit cells. Intermolecular forces are relatively weak. London Forces and D-D. |
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| Covalent Solids |
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| Individual atoms are covalently bonded to several other atoms; thus they are very hard with very high melting points. Diamond, graphite, SO2 (sand), SiC. Molecular less than Metallic less than Ionic less than Covalent |
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| Two major factors affect dissolution of solutes |
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| Enthalpy and Entropy |
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| Crystal Lattice Energy |
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| Measure of attractive forces among particles of a solid. Increases as the charges on ions increase. The higher the CLE, the stronger the bond. |
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| Enthalpy |
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| Change of energy content of solution (ChangeHsoln). If change Hsoln is exothermic (<0), dissolution is favored. -changeH |
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| Entropy |
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| Change in disorder (randomness( of the solution. ChangeSmixing. NaCl --> Na+ + Cl- increasing entropy +changeS |
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| Molality |
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| mol solute/kg solvent |
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| Molarity |
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| mol solute/L solution |
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| Mole Fraction |
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| Xa=(# mols of A)/(# mols of A + # mols of B) |
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| Percent by Mass |
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| g solute/100 g solution |