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4 NH3(g) + 3 O2(g) → 2 N2(g) + 6 H2O(g) If the standard molar heats of formation of ammonia, NH3(g),Thermodynamics Chemistry Question

Question

4 NH3(g) + 3 O2(g) → 2 N2(g) + 6 H2O(g)

If the standard molar heats of formation of ammonia, NH3(g), and gaseous water, H2O(g), are -46 kJ/mol and -242 kJ/mol, respectively, what is the value of ΔH°298 for the reaction represented above?

A.

-190 kJ/molrxn

B.

-290 kJ/molrxn

C.

-580 kJ/molrxn

D.

-1,270 kJ/molrxn

✓ Correct
E.

-1,640 kJ/molrxn

💡 Solution & Explanation

STEPS:

1. Recall the standard enthalpy of reaction formula: The standard enthalpy of a reaction (ΔH\Delta H^\circ) can be calculated from the standard enthalpies of formation (ΔHf\Delta H^\circ_f) of the reactants and products using Hess's Law:
ΔHrxn=nΔHf(products)mΔHf(reactants)\Delta H^\circ_{rxn} = \sum n \Delta H^\circ_f(\text{products}) - \sum m \Delta H^\circ_f(\text{reactants})
2. Identify the standard enthalpies of formation for elements: By definition, the standard enthalpy of formation of pure elements in their standard states is zero. Therefore:
* ΔHf(O2(g))=0 kJ/mol\Delta H^\circ_f (\text{O}_2(g)) = 0\text{ kJ/mol}
* ΔHf(N2(g))=0 kJ/mol\Delta H^\circ_f (\text{N}_2(g)) = 0\text{ kJ/mol}
3. Set up the summation with stoichiometric coefficients: Plug the coefficients from the balanced chemical equation (4 NH3(g)+3 O2(g)2 N2(g)+6 H2O(g)4\text{ NH}_3(g) + 3\text{ O}_2(g) \rightarrow 2\text{ N2}(g) + 6\text{ H}_2\text{O}(g)) into the Hess's Law expression:
ΔHrxn=[2×ΔHf(N2)+6×ΔHf(H2O)][4×ΔHf(NH3)+3×ΔHf(O2)]\Delta H^\circ_{rxn} = [2 \times \Delta H^\circ_f(\text{N}_2) + 6 \times \Delta H^\circ_f(\text{H}_2\text{O})] - [4 \times \Delta H^\circ_f(\text{NH}_3) + 3 \times \Delta H^\circ_f(\text{O}_2)]
4. Substitute the given values into the equation:
ΔHrxn=[2(0)+6(242)][4(46)+3(0)]\Delta H^\circ_{rxn} = [2(0) + 6(-242)] - [4(-46) + 3(0)]
5. Simplify the mathematical terms:
* Products: 6×(242)=1452 kJ/mol6 \times (-242) = -1452\text{ kJ/mol}
* Reactants: 4×(46)=184 kJ/mol4 \times (-46) = -184\text{ kJ/mol}
6. Subtract the reactant total from the product total:
ΔHrxn=1452(184)=1452+184=1268 kJ/molrxn\Delta H^\circ_{rxn} = -1452 - (-184) = -1452 + 184 = \mathbf{-1268\text{ kJ/mol}_{rxn}}
Rounding to three significant figures gives 1,270 kJ/molrxn-1,270\text{ kJ/mol}_{rxn}, which matches Option D.

*

WHY_OTHERS_WRONG:

  • A is incorrect: This value (~190 kJ/mol-190\text{ kJ/mol}) is close to 196 kJ/mol-196\text{ kJ/mol}, which is obtained if a student neglects the stoichiometric coefficients entirely and simply subtracts the two given formation values: (242)(46)(-242) - (-46).
  • B is incorrect: This value (~290 kJ/mol-290\text{ kJ/mol}) is close to 288 kJ/mol-288\text{ kJ/mol}, which a student would get by adding the two given enthalpies of formation directly without accounting for stoichiometry or the subtraction required by the Hess's Law formula: (242)+(46)(-242) + (-46).
  • C is incorrect: This value is approximately double the incorrect sum from option B, representing another failure to correctly apply stoichiometric balancing to the Hess's Law formula.
  • E is incorrect: This value (~1,640 kJ/mol-1,640\text{ kJ/mol}) is close to 1636 kJ/mol-1636\text{ kJ/mol}, which is the result of adding the reactant term and product term magnitudes instead of subtracting them: 1452184-1452 - 184. This represents a sign error during subtraction.
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