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Chapter 16. Reaction Energy. Thermochemistry. The study of the transfers of energy as heat that accompany chemical reactions and physical changes. Heat and Temperature. Calorimeter – measures the energy absorbed or released as heat in a chemical or physical change.
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Chapter 16 Reaction Energy
Thermochemistry • The study of the transfers of energy as heat that accompany chemical reactions and physical changes.
Heat and Temperature • Calorimeter – measures the energy absorbed or released as heat in a chemical or physical change. • Temperature – measures the average kinetic energy of the particles in a sample of matter. • Greater the kinetic energy of the particles in a sample, the higher the temperature is and the hotter it feels. • Joule – unit of heat as well as all other forms of energy. • Heat – energy transferred between samples of matter. (moves spontaneously from matter at a high temperature to matter of a lower temperature.
Specific Heat – quantity of heat required to raise the temperature of one gram of a substance by one degree Celsius. • The quantity of energy transferred as heat during a temperature change depends on the nature of the material changing temperature, the mass of the material changing temperature, and the size of the temperature change. • The difference depends on the metal’s differing capacities for absorbing this energy. • A quantity called specific heat can be used to compare heat absorption capacities for different materials. • cp = q / m x delta T (Specific heat at a given pressure) • q = cp x m x delta T (Quantity of energy gained or lost with a change in temperature.)
Enthalpy of Reaction pg534 • The energy absorbed as heat during a chemical reaction at constant pressure is represented by delta H. • Enthalpy Change – amount of energy absorbed by a system as heat during a process at constant pressure. • Delta H = Hproducts – Hreactants • Enthaply of Reaction is the quantity of energy transferred as heat during a chemical reaction. (Heat of reaction)
Thermochemical Equation pg535 • An equation that includes the quantity of energy released or absorbed as heat during the reaction. • Examples: • 2H2(g) + O2(g) 2H2O(g) + 483.6 kJ (exothermic) • Enthaply change is negative = energy released • Delta H = - 483.6 kJ • 2H2O(g) + 483.6 kJ 2H2(g) + O2(g) (endothermic) • Enthaply change is positive = energy absorbed • Delta H = + 483.6 kJ • See rules: pg 537
Enthalpy of Formation pg537 • Formation of a compound from its elements in their standard form. • The molar enthalpy of formation is the enthalpy change that occurs when one mole of a compound is formed from its elements in their standard state at 25oC and 1 atm. • Delta Hof • Appendix Table A-14 pg 862
Enthalpy of Reaction Calculations pg 539 • Pg.552 Problem 15a • -1207.6 -634.9 -393.5 • CaCO3(s) -------> CaO(s) + CO2(g) • -1207.6 0 0 0 • CaCO3 ------- Ca + C + 3/2O2 Hf0 = +1207.6 kJ • 0 0 -634.9 • Ca + 1/2O2 - CaO Hf0 = -634.9 kJ • 0 0 -393.5 • C + O2 --- CO2 Hf0 = -393.5 kJ • __________________________________________ • CaCO3(s) ------ CaO(s) + CO2(g) H = +179.2 kJ • (endothermic and unstable) • Hint: Hf0 = heat of formation • + = endothermic • - = exothermic • More negative the enthalpy of formation is, the more stable a compound is.
Driving Force of Reactions • Two factors that determines if a reaction will occur spontaneously (Define spontaneously?): • Change in energy • Randomness of the particles • Tendencies (Enthalpy + Reaction): • Exothermic: energy released, less energy in products, products resist to change, more stable. Natural direction that leads to a lower energy state. • Endothermic: energy absorbed, not spontaneous, products are at higher potential energy, and are less stable. Need outside influence (heat etc..) to proceed. • Tendencies (Entropy + Reaction): • Increase [(+) delta S] in randomness (entropy) reaction is spontaneous.
Free Energy • Processes in nature are driven in two directions: toward least enthalpy and toward largest entropy. When these two oppose each other, the dominant factor determines the direction of change. This combined enthalpy-entropy function is called the free energy, G, of the system; it is also called Gibbs free energy. • Natural processes proceed in the direction that lowers the free energy of a system. • Only the change in free energy can be measured. • Delta G0 = delta H0 – T delta S0 • The reaction will be spontaneous if you have a negative delta G. • The reaction will not be spontaneous if you have a positive delta G. • Another option: See table 2 pg 549