Reactivity 1. What drives chemical reactions?
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1.1 Measuring enthalpy changes
• Chemical reactions transfer energy between system and surroundings • Total energy conserved • Heat vs. temperature
• Endothermic: energy absorbed (T decreases) • Exothermic: energy released (T increases)
• Relative stability determines endo/exothermic nature • Energy profiles • Sketch and interpret labelled energy profiles for endothermic and exothermic reactions
• Heat transferred at constant pressure, standard conditions • Q = mcΔT • ΔH = −Q/n • Calculate enthalpy change from calorimetry data
1.2 Energy cycles
• Bond-breaking absorbs energy • Bond-forming releases energy • Calculate enthalpy change from average bond enthalpies
• Enthalpy change independent of pathway • Apply Hess's law to multistep reaction cycles
• Combustion: ΔHc⦵ • Formation: ΔHf⦵ • Deduce equations and solve problems using standard enthalpy data
• ΔH⦵ = ΣΔHf⦵(products) − ΣΔHf⦵(reactants) • ΔH⦵ = ΣΔHc⦵(reactants) − ΣΔHc⦵(products)
• Energy changes in ionic compound formation • Univalent and divalent ions • Interpret and determine cycle values; include lattice enthalpy and electron affinity terms
1.3 Energy from fuels
1.3.1Combustion reactions
• Reactive metals, non-metals, organic compounds + O₂ • Deduce complete combustion equations for hydrocarbons and alcohols
1.3.2Incomplete combustion
• Produces CO and C • Deduce incomplete combustion equations for hydrocarbons and alcohols
1.3.3Fossil fuels
• Coal, crude oil, natural gas • CO₂ emissions and greenhouse effect • Compare fuels by carbon dioxide released and energy output
1.3.4Biofuels
• From biological carbon fixation (photosynthesis) • Renewable vs. non-renewable • Consider advantages and disadvantages of biofuels compared with fossil fuels
1.3.5Fuel cells
• Convert chemical energy directly to electrical energy • Half-equations for electrode reactions • Include hydrogen and methanol fuel cells; PEM details are not assessed
1.4.1(HL)—Entropy (S)
• Measure of dispersal of matter/energy • More energy distributions = higher entropy • Order: Sgas > Sliquid > Ssolid • Calculate ΔS⦵ from S⦵ values
1.4.2(HL)—Gibbs energy (ΔG)
• ΔG⦵ = ΔH⦵ − TΔS⦵ • Relates energy from reaction to ΔH, ΔS, T
1.4.3(HL)—Spontaneity
• Spontaneous when ΔG < 0 • Temperature at which reaction becomes spontaneous • Interpret signs of ΔG from thermodynamic data
1.4.4(HL)—Equilibrium and Gibbs energy
• At equilibrium: ΔG = 0 • ΔG = ΔG⦵ + RT ln Q • ΔG⦵ = −RT ln K • Link ΔG, Q, and K to reaction direction and equilibrium position