Thermodynamics: Enthelpy of Sucrose

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SUMMARY

The discussion centers on calculating the enthalpy change (ΔH0) for the combustion of sucrose (C12H22O11) using data from a bomb calorimeter experiment. A mass of 0.1265 g of sucrose was burned, resulting in a temperature increase of 1.743 K, requiring 2.0823 kJ of energy. The molar enthalpy of formation for sucrose is provided as -2220 kJ/mol, which is essential for comparison with the calculated ΔH0 values. The calculations involve applying the equations for ΔH and ΔU, emphasizing the need to consider constant pressure conditions for accurate results.

PREREQUISITES
  • Understanding of thermodynamic concepts such as enthalpy (ΔH) and internal energy (ΔU).
  • Familiarity with calorimetry and the operation of bomb calorimeters.
  • Knowledge of the ideal gas law and its application in thermodynamic calculations.
  • Ability to interpret and utilize thermodynamic tables, specifically for molar enthalpy of formation.
NEXT STEPS
  • Calculate the heat of combustion of sucrose using the bomb calorimeter data.
  • Learn how to apply the equation ΔH = ΔU + PΔV in practical scenarios.
  • Study the implications of using ideal gas assumptions in thermodynamic calculations.
  • Explore the differences between constant volume and constant pressure measurements in calorimetry.
USEFUL FOR

Chemistry students, thermodynamics researchers, and professionals involved in calorimetry and energy calculations will benefit from this discussion.

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Homework Statement



A sample of sucrose, C12H22O11, with mass 0.1265 g, is burned in a bomb calorimeter initially at 298 K. The temperature rises by 1.743 K. To produce the same temperature increase with an electrical heater in this apparatus, it is found to require 2.0823 kJ of energy.

(1) Determine Δ H0 (298) for combustion of sucrose.

(2) Use data in Table 19.2 to calculate Δ H0 (298) for combustion of sucrose, and compare
your answer to (1).

(Table 19.2 states that Sucrose has a Molar Enthalpy of formation of -2220 kJ/Mol)

Homework Equations



DeltaH = DeltaU + Delta n R T

DeltaH = DeltaU + P DeltaV

U = Heat(constant v)

H = Heat(constant p)

Molar mass of Sucrose
Personal Assumption (Ideal gas?)

The Attempt at a Solution


So, I've tried a few things.

First I tried saying that the combustion of Sucrose is from 12 mol O2+ 1 mol Sucrose = 12 mol CO2 + H2O, thus delta n = 11 moles. Delta U is the energy from the problem statement because in the calorimeter the combustion is taking place at constant volume.

But if I use this, then my Delta H is in terms of a constant volume measurement, which apparently isn't what we're supposed to use, because Delta H is usually calculated via constant pressure. Even then, the molar value of Enthalpy is 79314.6 kJ/mol, which even for a big molecule, seems absurd compared to the value in the table for the next part of the problem.

I think the big part is that I'm assuming Ideal gas for the product gases. Is there any way out of this mess?
 
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Start by calculating the heat of combustion of sucrose in the bomb. How many moles of sucrose were burned? How much energy was released? What is the energy per mole?


In your expression for Delta U, what is the value of the term 'P Delta V' in that expression?
 

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