The document discusses the calculation of enthalpy change (ΔH) for chemical reactions using bond enthalpy data. It provides examples of using bond enthalpy values to calculate the ΔH for three reactions: 1) the combustion of methane, 2) the hydrogenation of ethylene, and 3) the fluorination of ethylene. For each reaction, it lists the bonds broken and formed, along with the associated bond enthalpy values. It then calculates the ΔH as the sum of the energies of bonds broken minus the sum of energies of bonds formed.
The document discusses the calculation of enthalpy change (ΔH) for chemical reactions using bond enthalpy data. It provides examples of using bond enthalpy values to calculate the ΔH for three reactions: 1) the combustion of methane, 2) the hydrogenation of ethylene, and 3) the fluorination of ethylene. For each reaction, it lists the bonds broken and formed, along with the associated bond enthalpy values. It then calculates the ΔH as the sum of the energies of bonds broken minus the sum of energies of bonds formed.
The document discusses the calculation of enthalpy change (ΔH) for chemical reactions using bond enthalpy data. It provides examples of using bond enthalpy values to calculate the ΔH for three reactions: 1) the combustion of methane, 2) the hydrogenation of ethylene, and 3) the fluorination of ethylene. For each reaction, it lists the bonds broken and formed, along with the associated bond enthalpy values. It then calculates the ΔH as the sum of the energies of bonds broken minus the sum of energies of bonds formed.
From this structure we can see that the bonds 35 2H2(g) + O2(g) → 2H2O(g)
broken are six C–H bonds and one C–C bond.
Bonds ΔH / kJ mol–1 Bonds H / kJ mol–1 33 B The bond enthalpy is the energy required broken (endothermic) formed (exothermic) to homolytically break 1 mole of bonds O=O +498 in gaseous molecules under standard 2H–H 2 × (+ 436) 4 × O–H 4 × (–464) conditions. The bond enthalpy of the C≡O bond is therefore represented by B, CO(g) → Total = +1370 = –1856 C(g) + O(g). ΔH = ΣE(bonds broken) – ΣE(bonds formed) = A and C are wrong because the products (+1370 + (–1856)) kJ mol–1 = –486 kJ mol–1 formed must also be in the gaseous state (Answers will vary slightly depending on the and C(s) is present. C and D are wrong values used! The bond enthalpy for the O–H because the equations also represent the bond given with the question differs from that in formation of O=O bonds with O2(g) as a Section 11 of the IB data booklet.) product. 36 B The reaction for the hydrogenation of a 34 H2C=CH2 + H2 → H3C–CH3 double bond is ΔH = ΣE(bonds broken) – ΣE(bonds formed) –CH=CH– + H2 → –CH2–CH2– Bonds ΔH / kJ mol –1 Bonds H / kJ mol –1
broken (endothermic) formed (exothermic) C=C +612 C–C –(–347) C=C +612 C–C 347 4C–H 4 × (+413) 6 × C–H 6 × (–413) H–H +436 2 × C–H 2 × (–412) H–H +436 Total = +1048 = –1171 Total = +2700 = –2825 ΔH = ΣE(bonds broken) – ΣE(bonds formed) ΔH = ΣE(bonds broken) – ΣE(bonds formed) = = (+1048 + (–1171)) kJ mol–1 = –123 kJ (+2700 + (–2825)) kJ mol–1 = –125 kJ mol–1 mol–1 This is the full method, and is totally correct. (Note that the bond enthalpies given in the However, it is simpler to ‘cancel out’ the four question differ from those in Section 11 of unchanged C–H bonds: the IB data booklet.) Bonds ΔH / kJ mol–1 Bonds H / kJ mol–1 37 C C2H4(g) + F2(g) → CH2FCH2F(g) broken (endothermic) formed (exothermic)
broken (endothermic) formed (exothermic) 2 × C–H 2 × (–413) C=C +612 C–C –347 H–H +436 4C–H 4 × (+436) 4 × C–H 4 × (–436) Total = +1048 = –1173 F–F 158 2 × C–F 2 × (–467) ΔH = ΣE(bonds broken) – ΣE(bonds formed) = Total = +2514 = –3025 (+1048 + (–1173)) kJ mol–1 = –125 kJ mol–1 (Answers will vary slightly depending on the ΔH = ΣE(bonds broken) – ΣE(bonds formed) values used! The bond enthalpies given with the = (+2514 + (–3025)) kJ mol–1 = –511 kJ question differ from those in Section 11 of the IB mol–1 data booklet.) (Note that the bond enthalpies given in the question on page 234 differ from 6