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CHEM 126 Final

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Question
Answer
Ion-Dipole force   - strength depends on charge density & size of ion (stronger as charge of ion or magnitude of dipole increases) - most commonly found in solutions - positive (cation) attracts partially negative & anion (anion) attracts partially negative - EX: h20 + N  
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Dipole - Dipole force   attractive forces between positive end of 1 polar molecule & negative end of another polar molecule - weaker than ionic & covalent bonds (only significant when touching) - EX: I + Cl  
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Ion Induced Dipole force   - ion induces a dipole of an atom/in a nonpolar molecule (disrupt e- arrangement in nonpolar specieis --> form a dipole) - EX: Fe+2 induces 02  
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Dipole Induced Dipole force   - polar molecules induce a dipole in an atom/in a nonpolar molecule (disrupt e- arrangement in nonpolar species) - EX: ethanol (polar) induces I2 (nonpolar)  
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Hydrogen Bond   - strongest bond - H + (N, O, or F) - H has high + charge density & high - charge density  
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Dispersion Forces   - NON POLAR molecules induce dipolse on each other - ex: oils, gas, unfamiliar forms of substance - polarizable e-clouds  
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range of attraction strength   1. ionic 2. covalent 3. ion-dipole 4. hydrogen bonding 5. dispersion forces 6. dipole-dipole 7. ion-induced dipole 8. dipole-induced dipole  
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properties of a solid   high intermolecular forces, low KE, high PE  
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properties of a liquid   medium intermolecular forces, equal KE and PE  
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properties of a gas   low intermolecular forces, high KE and low PE  
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melt/fusion   solid to liquid (increase temp) q = n(∆H°fus)  
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freeze   liquid to solid (decrease temp) q = n(-∆H°fus)  
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vaporize/boil   liquid to gas (increase temp) q = n(∆H°vap)  
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condensation   gas to liquid (decrease temp) q = n(-∆H°vap)  
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sublimation   solid to gas (increase temp)  
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deposition   gas to solid (decrease temp)  
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vapor pressure   - liquid gas equilibium - high vapor pressure --> evaporate more quickly - system will adjust rates of vapor/condensation to return to same vapor pressure  
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boiling point   vapor pressure = external, varies with altitude due to pressure change  
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melting/freezing point   - solid liquid equilibrium, pressure has no effect  
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PHASE DIAGRAM   - line between two phases = where at equilibrium - triple point = all at equilibrium - critical point = when equilibrium between liquid and gas becomes non-existent and turns into state in between both  
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surface tension   -energy required to increase the surface area (J/m2) - increase SA -> molecules move up to exterior by breaking attractions in the interior - stronger intermolecular forces -> more energy to increase SA -> more surface tension  
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capillarity   - rising of a liquid against the pull/gravity through a narrow space - competition between IMAFs within a liquid & those between the liquid & tube walls  
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concave up vs. concave down meniscus   - UP: IMAFs are stronger within substance vs between the substance & glass - DOWN: IMAFs from substance and glass form adhesive bonds with glass, cohesion forces between glass & substance  
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polar & nonpolar surface interaction   - adhesive forces between nonpolar (dipole induced dipole) are weaker than polar (H-bonds)-> pull away - EX: h20 & non polar surface  
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Viscosity   - resistance of a fluid to flow - results from IMAFs that impeded movement of molecules around and past each other - liquid > gas(more places for IM forces to act)  
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external effects on viscosity   - TEMP: v decreases with increased temp - MOLECULAR SHAPE: small/sphere - little contact, pour easily VS. long/large - more contact & pour slower  
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bond length & covalent radius   - bond length: between two bonded atoms in the SAME MOLECULE - 1/2 bond length = covalent raidus  
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van der waals distance & radius   - raidus: distance between nuclei of identical nonbonded atom, always larger than covalent radius - radii decreases across a period and increases down a group  
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