Bond energy calculation — find ΔH of reaction from bond dissociation energies

medium CBSE JEE-MAIN NEET NCERT Class 11 3 min read

Question

Calculate the enthalpy of the reaction CH4(g)+2O2(g)CO2(g)+2H2O(g)\text{CH}_4(g) + 2\text{O}_2(g) \rightarrow \text{CO}_2(g) + 2\text{H}_2\text{O}(g) using bond dissociation energies. Given: C-H = 413 kJ/mol, O=O = 498 kJ/mol, C=O = 799 kJ/mol, O-H = 463 kJ/mol.

(NCERT Class 11, Chapter 6)


Solution — Step by Step

In CH4\text{CH}_4: 4 C-H bonds broken

In 2O22\text{O}_2: 2 O=O bonds broken

Energy absorbed (bonds broken):

ΔHbroken=4×413+2×498=1652+996=2648 kJ\Delta H_{broken} = 4 \times 413 + 2 \times 498 = 1652 + 996 = 2648 \text{ kJ}

In CO2\text{CO}_2: 2 C=O bonds formed

In 2H2O2\text{H}_2\text{O}: 2×2=42 \times 2 = 4 O-H bonds formed

Energy released (bonds formed):

ΔHformed=2×799+4×463=1598+1852=3450 kJ\Delta H_{formed} = 2 \times 799 + 4 \times 463 = 1598 + 1852 = 3450 \text{ kJ}
ΔHrxn=Energy absorbedEnergy released\Delta H_{rxn} = \text{Energy absorbed} - \text{Energy released} ΔHrxn=ΔHbrokenΔHformed\Delta H_{rxn} = \Delta H_{broken} - \Delta H_{formed} ΔHrxn=26483450\Delta H_{rxn} = 2648 - 3450 ΔHrxn=802 kJ/mol\boxed{\Delta H_{rxn} = -802 \text{ kJ/mol}}

The negative sign confirms this is an exothermic reaction — consistent with combustion of methane.


Why This Works

Bond breaking requires energy (endothermic), while bond formation releases energy (exothermic). The enthalpy of a reaction is the net balance: if more energy is released in forming new bonds than is consumed in breaking old bonds, the reaction is exothermic.

The formula ΔH=Σ(BDE of bonds broken)Σ(BDE of bonds formed)\Delta H = \Sigma(\text{BDE of bonds broken}) - \Sigma(\text{BDE of bonds formed}) works because we are imagining a hypothetical path: first break all bonds in the reactants (go to atoms), then form all bonds in the products (come back from atoms). By Hess’s law, the enthalpy change depends only on the initial and final states, not the path.


Alternative Method

You can also use standard enthalpies of formation (ΔHf°\Delta H_f°) if available:

ΔHrxn=ΣΔHf°(products)ΣΔHf°(reactants)\Delta H_{rxn} = \Sigma \Delta H_f°(\text{products}) - \Sigma \Delta H_f°(\text{reactants})

This gives a more accurate result because bond energies are averages and can vary slightly depending on the molecular environment.

For JEE, memorise these common bond energies: C-H (413), C-C (348), C=C (614), C=O (799), O-H (463), O=O (498), N-H (391), H-H (436). With these, you can handle almost every bond energy numerical that appears.


Common Mistake

The most frequent error is reversing the formula — writing ΔH=bonds formedbonds broken\Delta H = \text{bonds formed} - \text{bonds broken} instead of bonds brokenbonds formed\text{bonds broken} - \text{bonds formed}. Remember: breaking bonds costs energy (positive), forming bonds releases energy (negative). The formula is ΔH=ΣBDEreactantsΣBDEproducts\Delta H = \Sigma BDE_{\text{reactants}} - \Sigma BDE_{\text{products}}. If you get a positive value for combustion, you have flipped the sign.

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