1. Chapter 8 Chapter 8 Thermochemistry: Chemical Energy

2. Energy and Its Conservation Units: 1 Cal = 1000 cal = 1 kcal 1 cal = 4.184 J (exactly) Energy: The capacity to supply heat or do work. Kinetic Energy (E K ): The energy of motion. Potential Energy (E P ): Stored energy. Thermal Energy: The kinetic energy of molecular motion and is measured by finding the temperature of an object Heat: The amount of thermal energy transferred from one object to another as the result of a temperature difference between the two

3. 8.2 Internal Energy and State Functions First Law of Thermodynamics: The total internal energy E of an isolated system is constant - The sum of all the kinetic and potential energies of particles making up a substance  E = E final - E initial

4. Systems and Surroundings System = the object in question Surrounding(s) = everything outside the system When both system and surrounding at same temperature thermal equilibrium When not Heat transfer to surrounding = exothermic (you feel the heat) hot metal!! Heat transfer to system = endothermic (you feel cold) cold metal!!

5. Internal Energy and State Functions State Function: A function or property whose value depends only on the present state, or condition, of the system, not on the path used to arrive at that state

6. 8.3 Expansion Work 3CO 2 (g) + 4H 2 O(g)C 3 H 8 (g) + 5O 2 (g) 7 mol of gas 6 mol of gas w = F x d = - P∆V Expansion Work: Work done as the result of a volume change in the system

7. 8.4 Energy and Enthalpy Constant Pressure:  E = q + w w = work = -P  V q = heat transferred q =  E + P  V q P =  E + P  V Constant Volume (  V = 0): q V =  E

8. Energy and Enthalpy = H products - H reactants Enthalpy change or Heat of reaction (at constant pressure) q P =  E + P  V =  H  H = H final - H initial Enthalpy is a state function whose value depends only on the current state of the system, not on the path taken to arrive at that state.

9. 8.6The Thermodynamic Standard State 3CO 2 (g) + 4H 2 O(g)C 3 H 8 (g) + 5O 2 (g) 3CO 2 (g) + 4H 2 O(l)C 3 H 8 (g) + 5O 2 (g)  H = -2219 kJ Thermodynamic Standard State: Most stable form of a substance at 1 atm pressure and at a specified temperature, usually 25 °C; 1 M concentration for all substances in solution. Standard enthalpy of reaction is indicated by the symbol ΔH o 3CO 2 (g) + 4H 2 O(g)C 3 H 8 (g) + 5O 2 (g)  H= -2043 kJ  H° = -2043 kJ

10. Enthalpies of Physical and Chemical Change

11. Enthalpy of Fusion (  H fusion ): The amount of heat necessary to melt a substance without changing its temperature Enthalpy of Vaporization (  H vap ): The amount of heat required to vaporize a substance without changing its temperature Enthalpy of Sublimation (  H subl ): The amount of heat required to convert a substance from a solid to a gas without going through a liquid phase

12. Enthalpies of Physical and Chemical Change 2Al(s) + Fe 2 O 3 (s)2Fe(s) + Al 2 O 3 (s)  H o = +852 kJ 2Fe(s) + Al 2 O 3 (s)2Al(s) + Fe 2 O 3 (s)  H o = -852 kJ endothermic exothermic The reverse reaction

13. Applying Stoichiometry to Heats of Reaction A propellant for rockets is obtained by mixing the liquids hydrazine, N 2 H 4, and dinitrogen tetroxide, N 2 O 4. These compounds react to give gaseous nitrogen, N 2 and water vapor, evolving 1049 kJ of heat at constant pressure when 1 mol N 2 O 4 reacts. a. Write the thermochemical equation for this reaction b. Write the thermochemical equation for the reverse of the reaction c. How much heat evolves when 10.0 g of hydrazine reacts according to the reaction described in (a) ?

14. Example An LP gas tank in a home barbeque contains 13.2 kg of propane, C 3 H 8. Calculate the heat (in kJ) associated with the complete combustion of all of the propane in the tank C 3 H 8 (g) + CO 2 (g)  3 CO 2 (g) + 4 H 2 O(g) ΔH o = -2044kJ

15. 8.6 Calorimetry The process of measuring heat transfer in at constant pressure (ΔH). chemical/physical process q rxn + q sol = 0 q rxn = -q sol R rxn = system S soln = surrounding What you’ll do in lab Heat given off by rxn Measured by thermometter Figure out q rxn indirectly

16. Calorimetry and Heat Capacity Measure the heat flow at constant volume (  E).

17. Calorimetry and Heat Capacity Specific Heat: The amount of heat required to raise the temperature of 1 g of a substance by 1 °C. q = (specific heat) x (mass of substance) x  T Molar Heat Capacity (C m ): The amount of heat required to raise the temperature of 1 mol of a substance by 1 °C. q = (C m ) x (moles of substance) x  T Heat Capacity (C): The amount of heat required to raise the temperature of an object or substance a given amount. q = C x  T

18. Calorimetry and Heat Capacity

19. Example How much heat must be added to a 8.21 g sample of gold to increase its temperature by 6.2 o C? The specific heat of gold is 0.13 J/g o C.

20. Example When 1.045 g of CaO is added to 50.0 mL of water at 25.0 o C in a calorimeter, the temperature of the water increases to 32.2 o C. Assuming that the specific heat of the solution is 4.18 J/g o C and that the calorimeter itself absorbes a negligible amount of heat, calculate ∆H in kilojoules for the reaction CaO(s) + H 2 O(l)  Ca(OH) 2 (aq)

21. 8.9Hess’s Law

22. Haber Process: Multiple-Step Process - Given N2H4(g)N2H4(g)2H 2 (g) + N 2 (g) Hess’s Law: The overall enthalpy change for a reaction is equal to the sum of the enthalpy changes for the individual steps in the reaction. 2NH 3 (g)3H 2 (g) + N 2 (g)  H° total = ???  H° 1 = 95.4 Kj 2NH 3 (g)N 2 H 4 (g) + H 2 (g)  H° total =  2NH 3 (g)3H 2 (g) + N 2 (g)  H° 2 = -187.6 kJ

23. Example Find ΔH o rxn for the following reaction C(s) + H 2 O(g)  CO(g) + H 2 (g) H o rxn = ? Use the following reactions with known H’s C(s) + O 2 (g)  CO 2 (g) ΔH o = -393.5 kJ 2CO(g) + O 2 (g)  2CO 2 (g) Δ H o = -566.0kJ 2H 2 (g) + O 2 (g)  2H 2 O (g) Δ H o = -483.6 kJ

24. Standard Heats of Formation Standard Heat of Formation (  H o f ): The enthalpy change for the formation of 1 mol of a substance in its standard state from its constituent elements in their standard states  H o f = -74.8 kJ CH 4 (g)C(s) + 2H 2 (g) Standard states 1 mol of 1 substance

25. Standard Heats of Formation cC + dDaA + bB Reactants Products  H o =  H o f (Products) -  H o f (Reactants)  H o = [c  H o f (C) + d  H o f (D)] - [a  H o f (A) + b  H o f (B)]

26. Standard Heats of Formation Using standard heats of formation, calculate the standard enthalpy of reaction for the photosynthesis of glucose (C 6 H 12 O 6 ) and O 2 from CO 2 and liquid H 2 O. C 6 H 12 O 6 (s) + 6O 2 (g)6CO 2 (g) + 6H 2 O(l)  H o = ?

27. Example Calculate the enthalpy change for the following reaction 3 NO 2 (g) + H 2 O(l)  2 HNO 3 (aq) + NO(g) *Use standard enthalpies of formation

28. An Introduction to Entropy Spontaneous Process: A process that, once started, proceeds on its own without a continuous external influence Entropy (S): The amount of molecular randomness in a system

29. An Introduction to Entropy Spontaneous processes are favored by a decrease in H (negative  H). favored by an increase in S (positive  S). Nonspontaneous processes are favored by an increase in H (positive  H). favored by a decrease in S (negative  S).

30. Example Predict whether ΔS o is likely to be positive or negative for each of the following reactions a.H 2 C=CH 2 (g) + Br 2 (g)  BrCH 2 CH 2 Br(l) b.Consider the following figures