A sample of solid dimethyl oxalate (C4H6O4) that weighs 1.431 g is burned in an excess of oxygen to CO2(g) and H2O() in a constant-volume calorimeter at 25.00 °C. The temperature rise is observed to be 2.140 °C. The heat capacity of the calorimeter and its contents is known to be 9.474×103 J K-1.
(a) Write and balance the chemical equation for the combustion reaction. Use the lowest possible coefficients. Use the pull-down boxes to specify states such as (aq) or (s). If a box is not needed, leave it blank.
(b) Assuming that H° is approximately equal to E, calculate the standard enthalpy change for the combustion of 1.000 mol of dimethyl oxalate to CO2(g) and H2O().
_________ kJ mol-1
(c) Calculate the standard enthalpy of formation per mole of dimethyl oxalate, using the following for the standard enthalpies of formation of CO2(g) and H2O().
Hf° H2O () = -285.83 kJ mol-1 ; Hf° CO2(g) = -393.51 kJ mol-1
________ kJ mol-1
(a)
2C2H6O4+7O2→8CO2+6H2O (b)
q=ccal×ΔT=9.474×103KJ×2.140K=20274.36J=20.274kJ
n(C4H6O4)=Mm=118.089molg1.431g=0.0121mol
ΔHc0=−nq=−0.0121mol20.274kJ=−1676molkJ (c)
C2H6O4+3.5O2→4CO2+3H2O
ΔHc0=∑ΔHf0(products)−∑ΔHf0(reactants)ΔHc0=(4×ΔHf0(CO2)+3×ΔHf0(H2O))−(3.5×Δhf0(O2)+ΔHf0(C4H6O4))
−1676molkJ=(4×(−393.51molkJ)+3×(−285.83molkJ))−(3.5×0molkJ+ΔHf0(C4H6O4))
ΔHf0(C4H6O4)=−755.53molkJ
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