Thermochemistry Notes For Finals
Thermochemistry Notes For Finals
184 J/g/k] q= mCT q= heat released or absorbed by solution m= mass of substance C= specific heat capacity (for water= 4.184 j g-1 K-1) T= Tf- Ti (change in temperature) Note: mass= density x volume (this is handy) Bomb Calorimeter- used for measuring energy released in a combustion reaction. Question: C6H12O6 + 6O2 6CO2 + 6H20(g) Hcombustion =-2808 KJ What is the final temperature of 50.0g of H2O in the calorimeter if 54.0g of glucose was combusted? The initial temperature of 25.0oC n(glucose)= 54/180= 0.3 mol glucose Hreleased rxn= 0.3 glucose x 2808KJ= 842.4KJ Now, Habsorbed by water= mcT 842400= (50.0)(4.184)( T) T= 4.03 Tfinal= 25+4.03= 29.03 Calculation component for Calorimetry: A. B. C. D. E. Heat absorbed by solution: [q= mCT] Heat absorbed by Calorimeter: [q= C x T] Total heat produced by the reaction: [q (total)= A +B] Enthalpy= Negative of heat produced in reaction ( - C) Molar enthalpy= [Enthalpy] / [moles of substance reacted]
Enthalpy (H): Heat content of a system at constant pressure Changes in energy (H) Hrxn= Hproducts- Hreactants Reactions releasing heat (EXOTHERMIC), H <0 Reactions absorbing heat (ENDOTHERMIC), H>0
Thermochemical Equations: - Balanced chemical equations that include physical states of all reactants and products of the energy change (H) 1. (Hformation >0) Ca(s) + C(s) + 3/2 O(g) CaCO3 (s) Na(s) + Br2(l) + 3/2 O2(g) NaBrO3(s) 2. Hcombustion <<0 Mg(s) + O2(g) MgO(s) C8H18(l) + 25/2 O2(g) 8CO2(g) + 9H2O(l) 3. Hdissociation H2(g) 2H(g) ; HCl(g) H(g) + Cl(g) 4. Hatomisation O2(g) O(g) 5. Hionisation First ionization enthalpy: atom(g) ion(+) (g) + e(-) (g) Second ionization enthalpy: ion(+) (g) ion(2+) (g) + e(-) (g) 6. Electron Affinities Atom(g) + e (-) ion(-) (g) O2(g) + e(-) O (2-) (g) Phase Transitions: 1. Solid Liquid H (fusion) = standard enthalpy of fusion or melting 2. Liquid gas H (vaporization)= standard enthalpy of vaporization 3. Solid gas H (sublimation)= standard of enthalpy of sublimation. Hess Law: States that the energy of a chemical reaction is the same regardless of the number of steps needed or the reaction mechanism. (H= ?)
Spontaneous: A physical or chemical change that occurs with no outside intervention of ordinary conditions (some energy may be supplied). - All exothermic rxns arent spontaneous: H2O(s)H2O(l) (H=+) endo. Spontaneity depends on a combination of : 1. Enthalpy (H) 2. Entropy (S) Heat of Formation (Hof) - Change of enthalpy that accompanies the formation of 1mol of the compound in their standard states. - Free elements in their standard states: (Hof)= 0.0KJ Heat of Fusion (Hfusion) - Energy needed for one gram of a solid to melt without any change in temperature. Heat of Vaporisation (Hvaporitation) q=mcT - Energy needed for one gram of a liquid to vaporize (boil) without a change in pressure. Phase diagram calculation: Q. How much energy will it take to heat 10.0g ice from -15 to 15oC? [C=4.184 for water) Solution: conduct q to each phase change and then add up the qs. Can use Hess law OR
Gibbs Free Energy (G)combined enthalpy/entropy function that determines spontaneity of process or the amount of energy that is left after a rxn occurs. Gibbs energy (G) the energy available to do work G= H TS G<0 (spontaneous) G>0 (non-spontaneous) H= exothermic H= endothermic T= is the thermodynamic temperature (K or) H= enthalpy of the system (KJ) S= entropy of the system (KJ/K)
1st Law of Thermodynamics: Conservation of energy. 2nd Law of Thermodynamics -Heat always flows from hot to cold objects never cold to hot.
3rd Law of Thermodynamics: -Entropies of all perfectly crystalline substances approach a common value as the temperature apporaches zero (OK). Entropy: - Measure the amount of disorder in a system. - Nature tends towards disorder, as time elapses (entropy increases) - Energy is required to decrease entropy/order.