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CHEM 126 Final

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Question
Answer
IMAFs on protein   - secondary: form shape - tertiary: overall 3D shape ** determines function - quanternary: arrangement of two or more polypeptide chains in protein  
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IMAFs on DNA   - created by nucleic acids, two chains wrapped around each other in a double helix - polar exterior: PO4 groups interact with ion dipole & h bonds - polar interior: N containing bases, interact by dispersion forces - h bonds: keep chains together  
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colloid   - dispersed (solute-like) substance distributed throughout a dispersing (solvent-like) substances - particles are larger than simple molecules but too small to settle out - EX: G-G (all gases) G-L (foam) L-L (milk) S-L (jelly)  
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Osmotic Pressure (concentration effects)   - increases with number of solute particles - OP = (n solute/ v solution) *RT * n = moles of solute, R = gas constant, T = temp, V = volume of solution)  
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Freezing Point (concentration effects)   - decreases with increasing solute particles -∆T f = ∆Kf*M *m = molality, Kf = freezing point depression constant, ∆Tf = Tf solvent - Tf solution - ∆T > 0 -> decrease in freezing point  
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Boiling Point (concentration effects)   - increases when solute particles increase - boiling point elevation: ∆Tb = Kb * m * Kb = boiling point elevation constant, m = molality, ∆Tb = Tb solution - Tb solvent  
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Vapor Pressure (concentration effects)   - decreases with number of particles of solute (more particles -> lower VP) -P solvent (∆P) = X solvent * P0 solvent * X solvent = 1 - X solute ∆P > 0 -> decrease in VP  
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Parts by Mass (or volume)   - Volume of solute (L)/ volume of solution (L) - composition  
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Mole Fraction   - amount of solute (mol)/ (amount of solute (mol) + amount of solution (mol)) -Vapor-Pressure Determination, Composition  
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Molality   - m - amount of solute (mol)/ mass of solvent (kg) - colligative behavior  
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Molarity   - M - (amount of solute (mol)/volume of solution (L)) - moles of solute that would be dissolved in 1 L of a solution - stoichiometry equations & analysis  
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Henry's Law   - determines gas solubility at given pressures - S gas = K h * P gas * s= solubility (mol/L) Kh = Henry's Law Constant, P = pressure  
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effect of pressure on solubility   - increase pressure -> increase GAS solubility - increase pressure -> decrease does not affect solid of liquid solubility  
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effect of temp on solubility   - increase temp -> increase solid solubility - increase temp -> decrease gas solubility  
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supersaturated   - amount dissolved is more than max dissolved possible - unstable solution & will easily seperate out  
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unsaturated   - amount dissolved is less than max dissolved possible  
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saturated   - max amount of dissolved solid - crystallization rate = dissolving rate  
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sontaneity   energy contribution - entropy contribution * help determine if process occurs spontaneously  
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entropy   distribution of energy over larger number of states  
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∆H equations   ∆H solution = ∆H solute + ∆ H solvation/hydration (always < 0) ∆H solvation = ∆H solvant + ∆H mixing ∆H solute = -∆H lattice (always > 0)  
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Solubility   - S - max amount that dissolveds in a fixed quantity of a given solvent at a given temp - excess of solute is present  
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different types of solution   L-S (salt water) L-L (gasoline) G-G (natural gas) G-L (soda) G-S (H2 + Pd) S-S (alloys)  
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2 substances form a solution?   ∆H = exothermic -> unfavorable, will not mix * breaking strong for weak ∆H = endothermic -> favorable & will mix * breaking weak for strong  
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