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CHAPTER 11 OUTLINE THERMOCHEMISTRY |
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I. The Flow of Energy - Heat A. Energy and Heat 1. Thermochemistry - heat changes that occur during chemical reactions 2. Energy - capacity to work/supply heat a. Detected only by effects b. Chemical Potential Energy - stored energy 1. Determined by type & arrangement of atoms 3. Heat (q) - energy transfer between objects due to temperature differences a. Flows from hot objects to cool objects b. Stops when temperatures are the same B. Exothermic and Endothermic Processes 1. System - part of universe focusing on 2. Surroundings - everything else 3. LAW OF CONSERVATION OF ENERGY a. Energy is neither created or destroyed, just changed 4. Endothermic reaction - system absorbs energy from surroundings 5. Exothermic reaction - system releases energy to surroundings |
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Endothermic | Exothermic | ||||||||||||||||||||||||||||||
Positive q | Negative q | ||||||||||||||||||||||||||||||
Gain of heat by system | |||||||||||||||||||||||||||||||
Loss of heat by system | |||||||||||||||||||||||||||||||
C. Heat Capacity 1. calorie (cal) - unit of heat and energy a. Def. - quantity of heat needed to raise the temperature of 1 gram of water 1 degree C b. 1,00 calories = 1 Calorie (used for dietary measuring) 2. Joule (J) - SI unit of heat and energy a. 1 cal = 4.18 J 3. Heat capacity info a. Depends on mass & chemical composition b. Increase mass, increase heat capacity c. Effects temperature of object 4. Specific Heat Capacity (Specific Heat) a. Def. - amount of heat needed to raise 1 gram of a substance 1 degree C b. Heat effects objects with low specific heat the most |
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Low specific heat | High specific heat | ||||||||||||||||||||||||||||||
Great temperature change | |||||||||||||||||||||||||||||||
Small temperature change | |||||||||||||||||||||||||||||||
c. Water moderates temperature d. Calculations C = q/(m delta T) 1. C = specific heat 2. m = mass 3. delta T = change in temperature (Tf - Ti) a. Tf = final temperature b. Ti = initial temperature II. Measuring and Expressing Heat Changes A. Calorimetry 1. Accurate & Precise measurement of heat change 2. Calorimeter - device used to measure amount of heat absorbed or lost 3. Enthalpy (H) - amount of heat of a substance at a given temperature and pressure a. Constant pressure, heat change (delta H) = q q = delta H = mCdeltaT 1. Exothermic = negative delta H 2. Endothermic = positive delta H B. Thermochemical Equations 1. Equations that include heat change CaO (s) + H2O (l) --> Ca(OH)2 (s) + 65.2 kJ a. State of matter is very important b. Changes amount of delta H 2. Heat of Reaction - heat change for the equation as written a. Assumed at 101.3 kPa and 25 degrees C 3. Problems work like stoichiometry problems Ex. 2 moles of CaO produces how much heat when reacted with water? Delta H = 2 mol X -65.2 kJ = -130.4 kJ (exothermic) 4. Heat of combustion - heat of reaction for completely burning one mole of a substance a. Calculate & reported like other heat of reactions III. Heat in Changes of State A. Heats of Fusion and Solidification 1. All phase changes involve absorbing or releasing heat at constant temperature q = delta H = mdeltaH(fus) [NO delta T) 2. Molar heat of fusion (deltaH{fus}) - heat absorbed by one mole of a substance melting at constant temperature 3. Molar heat of solidification (deltaH{solid}) - heat released by one mole of a substance freezing at constant temperature a. delta H(fus) = - delta H(solid) B. Heat of Vaporization and Condensation 1. Molar heat of vaporization (delta H {vap}) - heat absorbed by one mole of a substance evaporating at constant temperature 2. Molar heat of condensation (delta H{cond}) - heat released by one mole of a substance condensing at constant temperature a. delta H(vap) = - delta H(cond) C. Heat of Solution 1. Molar heat of solution (delta H{soln}) - heat change caused by dissolution of on mole of a substance a. Heat absorbed or released when dissolving solutes in solvents D. Important note: Molar heats are always in units of J/mol or kJ/mol, if the word Molar is removed (heat of ...) then the units are J/g or kJ/g IV. Calculating Heat Changes A. Hess's Law 1. Hess's Law of heat summation - If you add two or more thermochemical equations to make a new equation, then you can add the delta H values from each equation to get the new delta H value Ex. B. Standard Heats of Formation (delta H(f)o) 1. change in enthalpy (delta H) from the formation of one mole of a compound from its elements at 25 degrees C 2. Standard heat of reaction (delta Ho) can be calculated from the delta H(f)o of the reactants and products delta Ho = delta H(f)o (products) - delta H(f)o (reactants) Outline based upon: Matta, M. S., Staley, D. D., Waterman, E. L., & Wilbraham, A. C. (2000). Chemistry, Addison-Wesley (5th ed.). Menlo Park, CA: Prentice Hall. pp. 293-320. |
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