The bomb calorimeter in Exercise 108 is filled with \(987 \mathrm{~g}\) water. The initial temperature of the calorimeter contents is \(23.32^{\circ} \mathrm{C}\). A \(1.056-\mathrm{g}\) sample of benzoic acid \(\left(\Delta E_{\text {comb }}=-26.42 \mathrm{~kJ} / \mathrm{g}\right)\) is combusted in the calorimeter. What is the final temperature of the calorimeter contents?

Short Answer

Expert verified
The final temperature of the calorimeter contents is approximately \(16.91^{\circ}C\).

Step by step solution

01

Calculate the total heat released by the combustion of benzoic acid

To calculate the total heat released, we will multiply the mass of the benzoic acid sample and the heat of combustion per gram: \(q = m_{BA} \Delta E_{comb}\) where \(m_{BA}\) is the mass of benzoic acid sample and \(\Delta E_{comb}\) is the heat of combustion per gram. \(q = (1.056 g)\left(-26.42 \frac{kJ}{g}\right)\) First, convert kJ to J: \(q = (1.056 g)\left(-26.42 \frac{1000 J}{g}\right)\) Now, calculate q: \(q = -27,932.32 J\) The negative sign indicates that the heat is released during the combustion process.
02

Calculate the final temperature of the calorimeter contents using the heat transfer formula

Now, we will use the heat transfer formula to find the final temperature of the calorimeter contents. The heat released by the combustion of benzoic acid will be absorbed by the water in the calorimeter: \(q = m_{H2O}c\Delta T\) where \(m_{H2O}\) is the mass of water in the calorimeter and c is specific heat capacity of water. Substitute the values: \(-27,932.32 J = (987g)\left(4.184 \frac{J}{g^{\circ}C}\right)(T_f - 23.32^{\circ}C)\) Now, divide by the product of the mass of water and the specific heat capacity of water: \(\frac{-27,932.32 J}{(987g)(4.184 \frac{J}{g^{\circ}C})} = T_f - 23.32^{\circ}C\) Calculate the value on the left side: \(-6.41^{\circ}C = T_f - 23.32^{\circ}C\) Now, add the initial temperature to both sides: \(-6.41^{\circ}C + 23.32^{\circ}C = T_f\) Finally, calculate the final temperature: \(T_f = 16.91^{\circ}C\) The final temperature of the calorimeter contents is approximately \(16.91^{\circ}C\).

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Most popular questions from this chapter

At \(298 \mathrm{~K}\), the standard enthalpies of formation for \(\mathrm{C}_{2} \mathrm{H}_{2}(g)\) and \(\mathrm{C}_{6} \mathrm{H}_{6}(l)\) are \(227 \mathrm{~kJ} / \mathrm{mol}\) and \(49 \mathrm{~kJ} / \mathrm{mol}\), respectively. a. Calculate \(\Delta H^{\circ}\) for $$ \mathrm{C}_{6} \mathrm{H}_{6}(l) \longrightarrow 3 \mathrm{C}_{2} \mathrm{H}_{2}(g) $$ b. Both acetylene \(\left(\mathrm{C}_{2} \mathrm{H}_{2}\right)\) and benzene \(\left(\mathrm{C}_{6} \mathrm{H}_{6}\right)\) can be used as fuels. Which compound would liberate more energy per gram when combusted in air?

The enthalpy of combustion of \(\mathrm{CH}_{4}(\mathrm{~g})\) when \(\mathrm{H}_{2} \mathrm{O}(l)\) is formed is \(-891 \mathrm{~kJ} / \mathrm{mol}\) and the enthalpy of combustion of \(\mathrm{CH}_{4}(\mathrm{~g})\) when \(\mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) is formed is \(-803 \mathrm{~kJ} / \mathrm{mol} .\) Use these data and Hess's law to determine the enthalpy of vaporization for water.

One mole of \(\mathrm{H}_{2} \mathrm{O}(g)\) at \(1.00 \mathrm{~atm}\) and \(100 .^{\circ} \mathrm{C}\) occupies a volume of \(30.6 \mathrm{~L}\). When one mole of \(\mathrm{H}_{2} \mathrm{O}(g)\) is condensed to one mole of \(\mathrm{H}_{2} \mathrm{O}(l)\) at \(1.00 \mathrm{~atm}\) and \(100 .{ }^{\circ} \mathrm{C}, 40.66 \mathrm{~kJ}\) of heat is released. If the density of \(\mathrm{H}_{2} \mathrm{O}(l)\) at this temperature and pressure is \(0.996 \mathrm{~g} / \mathrm{cm}^{3}\), calculate \(\Delta E\) for the condensation of one mole of water at \(1.00 \mathrm{~atm}\) and \(100 .{ }^{\circ} \mathrm{C}\).

Photosynthetic plants use the following reaction to produce glucose, cellulose, and so forth: $$ 6 \mathrm{CO}_{2}(g)+6 \mathrm{H}_{2} \mathrm{O}(l) \stackrel{\text { Sunlight }}{\longrightarrow} \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s)+6 \mathrm{O}_{2}(g) $$ How might extensive destruction of forests exacerbate the greenhouse effect?

Given the following data $$ \begin{aligned} 2 \mathrm{ClF}(g)+\mathrm{O}_{2}(g) & \longrightarrow \mathrm{Cl}_{2} \mathrm{O}(g)+\mathrm{F}_{2} \mathrm{O}(g) & \Delta H &=167.4 \mathrm{~kJ} \\ 2 \mathrm{ClF}_{3}(g)+2 \mathrm{O}_{2}(g) & \longrightarrow \mathrm{Cl}_{2} \mathrm{O}(g)+3 \mathrm{~F}_{2} \mathrm{O}(g) & \Delta H &=341.4 \mathrm{~kJ} \\\ 2 \mathrm{~F}_{2}(g)+\mathrm{O}_{2}(g) & \longrightarrow 2 \mathrm{~F}_{2} \mathrm{O}(g) & \Delta H &=-43.4 \mathrm{~kJ} \end{aligned} $$ calculate \(\Delta H\) for the reaction $$ \mathrm{ClF}(g)+\mathrm{F}_{2}(g) \longrightarrow \mathrm{ClF}_{3}(g) $$

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