Question #81926

The standard enthalpies of formation, at 25.00degrees celsius, of methanol (CH4O (l)), water (H2O (l)), and carbon dioxide (CO2 (g)) are respectively -238.7 kJ / mol, - 285.8 kJ / mol, and -393.5 kJ / mol. Calculate the change in the surrounding entropy (in J / K) when burning 15.4 g of methanol under a constant pressure of 1,000 atm at 25.00 degrees celsius (combustion is the reaction of a substance with oxygen molecular to produce water and carbon dioxide).
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Expert's answer

2019-01-09T05:38:17-0500

Answer on Question #81926, Chemistry/ General Chemistry

The standard enthalpies of formation, at 25.00 degrees celsius, of methanol (CH4O (l)), water (H2O (l)), and carbon dioxide (CO2 (g)) are respectively -238.7 kJ/mol, -285.8 kJ/mol, and -393.5 kJ/mol. Calculate the change in the surrounding entropy (in J/K) when burning 15.4 g of methanol under a constant pressure of 1,000 atm at 25.00 degrees celsius (combustion is the reaction of a substance with oxygen molecular to produce water and carbon dioxide).

Solution

2CH3OH(l)+3O2(g)2CO2(g)+4H2O(l)2 \mathrm{CH_3OH} (l) + 3 \mathrm{O_2(g)} \rightarrow 2 \mathrm{CO_2(g)} + 4 \mathrm{H_2O(l)}


Calculate the standard enthalpy of this reaction


ΔHf0(CH4O(l))=238.7 kJ/mol\Delta H_f^0(\mathrm{CH_4O(l)}) = -238.7\ \mathrm{kJ/mol}ΔHf0(CO2(g))=393.5 kJ/mole.\Delta H_f^0(\mathrm{CO_2(g)}) = -393.5\ \mathrm{kJ/mole}.ΔHf0(H2O(l))=285.8 kJ/mol\Delta H_f^0(\mathrm{H_2O(l)}) = -285.8\ \mathrm{kJ/mol}ΔHf0(O2(g))=0 kJ/mol\Delta H_f^0(\mathrm{O_2(g)}) = 0\ \mathrm{kJ/mol}ΔHrxn0=Hf(products)0Hf(reactants)0\Delta H_{rxn}^0 = \sum H_{f(\text{products})}^0 - \sum H_{f(\text{reactants})}^0ΔHrxn0=[2 mol×Hf0(CO2(g))+4 mol×Hf0(H2O(l))][2 mol×Hf0(CH4O(l))+3 mol×Hf0(O2(g))]=[2 mol×(393.5 kJmol)+4 mol×(285.8 kJmol)][2 mol×(238.7 kJmol)+1 mol×(0 kJmol)]=1452.8 kJ\begin{aligned} \Delta H_{rxn}^0 &= \left[2\ \mathrm{mol} \times H_f^0(\mathrm{CO_2(g)}) + 4\ \mathrm{mol} \times H_f^0(\mathrm{H_2O(l)})\right] \\ &\quad - \left[2\ \mathrm{mol} \times H_f^0(\mathrm{CH_4O(l)}) + 3\ \mathrm{mol} \times H_f^0(\mathrm{O_2(g)})\right] \\ &= \left[2\ \mathrm{mol} \times \left(-393.5\ \frac{\mathrm{kJ}}{\mathrm{mol}}\right) + 4\ \mathrm{mol} \times \left(-285.8\ \frac{\mathrm{kJ}}{\mathrm{mol}}\right)\right] \\ &\quad - \left[2\ \mathrm{mol} \times \left(-238.7\ \frac{\mathrm{kJ}}{\mathrm{mol}}\right) + 1\ \mathrm{mol} \times \left(0\ \frac{\mathrm{kJ}}{\mathrm{mol}}\right)\right] = -1452.8\ \mathrm{kJ} \end{aligned}


Calculate the standard enthalpy of this reaction when 15.4 g of methanol is burned:


n=m/Mn = m/MM(CH4O)=32 g/molM(\mathrm{CH_4O}) = 32\ \mathrm{g/mol}n(CH4O)=15.4 g32 gmol=0.48 moln(\mathrm{CH_4O}) = \frac{15.4\ \mathrm{g}}{32\ \frac{\mathrm{g}}{\mathrm{mol}}} = 0.48\ \mathrm{mol}


Solve the proportion:

When 2 mol of methanol is burned ΔHrxn0=1452.8 kJ\Delta H_{rxn}^0 = -1452.8\ \mathrm{kJ}

When 0.48 mol of methanol is burned ΔHrxn0=x kJ\Delta H_{rxn}^0 = x\ \mathrm{kJ}

20.48=1452.8x\frac{2}{0.48} = \frac{-1452.8}{x}x=348.7kJx = -348.7 \, \text{kJ}ΔSsurroundings=ΔHT\Delta S_{\text{surroundings}} = -\frac{\Delta H}{T}ΔSsurroundigs=348700J(273+25)K=1170JK\Delta S_{\text{surroundigs}} = -\frac{-348700 \, \text{J}}{(273 + 25) \, \text{K}} = 1170 \, \frac{\text{J}}{\text{K}}


Answer: 1170 J/K

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