Consider a balloon filled with helium at the following conditions. $$ \begin{array}{l}{313 \mathrm{g} \mathrm{He}} \\ {1.00 \mathrm{atm}} \\ {1910 . \mathrm{L}} \\ {\text { Molar Heat Capacity }=20.8 \mathrm{J} / \mathrm{C} \cdot \mathrm{mol}}\end{array} $$ The temperature of this balloon is decreased by \(41.6^{\circ} \mathrm{C}\) as the volume decreases to \(1643 \mathrm{L},\) with the pressure remaining constant. Determine \(q, w,\) and $\Delta E(\text { in } \mathrm{kJ} \text { ) for the compression of }$ the balloon.

Short Answer

Expert verified
In the compression process of a helium-filled balloon with constant pressure, the heat (q) is -67 kJ, the work (w) is 10.9 kJ, and the change in internal energy (ΔE) is -56.1 kJ.

Step by step solution

01

Calculate the number of moles

To calculate the number of moles, we use the Ideal Gas Law. \[PV = nRT\] We know the mass m of helium is given (313 g) and the molar mass of helium is 4 g/mol. Therefore, the number of moles (n) can be calculated as: \[n = \frac{m}{M}\] \[n = \frac{313 \text{ g}}{4 \text{ g/mol}}\] \[n = 78.25 \text{ mol}\]
02

Calculate the initial temperature T1

Use the Ideal Gas Law again and solve for the initial temperature T1. \[PV = nRT\] Rearranging the equation for T1: \[T1 = \frac{PV}{nR}\] We know P = 1.00 atm, V = 1910 L, n = 78.25 mol, and R ≈ 0.0821 L·atm/K·mol. Now, we can plug the values into the equation. \[T1 = \frac{(1.00 \text{ atm})(1910 \text{ L})}{(78.25 \text{ mol})(0.0821 \text{ L·atm/K·mol})}\] \[T1 ≈ 298.6 \text{K}\]
03

Calculate the final temperature T2

We know that the temperature is decreased by 41.6°C, which is equivalent to 41.6 K. Therefore, we can find the final temperature T2: \[T2 = T1 - \Delta T\] \[T2 = 298.6 \text{ K} - 41.6 \text{K}\] \[T2 ≈ 257 \text{K}\]
04

Calculate heat q

Now, we can use the equation for heat to calculate q: \[q = nC\Delta T\] We have n = 78.25 mol, C = 20.8 J/C·mol, and ΔT = T2 - T1 = -41.6 K. \[q = (78.25 \text{ mol})(20.8 \text{ J/C·mol})(-41.6 \text{ K})\] \[q ≈ -6.7 \times 10^{4} \text{ J}\] Convert the value of q to kJ: \[q ≈ -67 \text{ kJ}\]
05

Calculate work w

To calculate work (w), we use the equation: \[w = -P\Delta V\] We have P = 1.00 atm, and we need to find ΔV. We are given the initial volume V1 = 1910 L, and the final volume V2 = 1643 L. \[\Delta V = V2 - V1\] \[\Delta V = 1643 \text{ L} - 1910 \text{ L}\] \[\Delta V = -267 \text{ L}\] Now, we can calculate w: \[w = -(1.00 \text{ atm})(-267 \text{ L})\] \[w ≈ 267 \text{ L·atm}\] Convert the value of w to kJ: \[w ≈ 10.9 \text{ kJ}\]
06

Calculate the change in internal energy ΔE

Using the First Law of Thermodynamics, we can now calculate the change in internal energy ΔE: \[\Delta E = q + w\] \[\Delta E = -67 \text{ kJ} + 10.9 \text{ kJ}\] \[\Delta E ≈ -56.1 \text{ kJ}\]
07

Final Answers

1. Heat (q): -67 kJ 2. Work (w): 10.9 kJ 3. Change in Internal Energy (ΔE): -56.1 kJ

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Most popular questions from this chapter

What is the difference between \(\Delta H\) and \(\Delta E ?\)

In a coffee-cup calorimeter, 50.0 \(\mathrm{mL}\) of 0.100\(M \mathrm{AgNO}_{3}\) and 50.0 \(\mathrm{mL}\) of 0.100 \(\mathrm{M} \mathrm{HCl}\) are mixed to yield the following reaction: $$\mathrm{Ag}^{+}(a q)+\mathrm{Cl}^{-}(a q) \longrightarrow \mathrm{AgCl}(s)$$ The two solutions were initially at \(22.60^{\circ} \mathrm{C}\) , and the final temperature is \(23.40^{\circ} \mathrm{C}\) Calculate the heat that accompanies this reacture in kJ/mol of AgCl formed. Assume that the combined solution has a mass of 100.0 \(\mathrm{g}\) and a specific heat capacity of 4.18 \(\mathrm{J} / \rho \mathrm{C} \cdot \mathrm{g} .\)

Consider the dissolution of \(\mathrm{CaCl}_{2} :\) $$ \mathrm{CaCl}_{2}(s) \longrightarrow \mathrm{Ca}^{2+}(a q)+2 \mathrm{Cl}^{-}(a q) \quad \Delta H=-81.5 \mathrm{kJ} $$ An 11.0 -g sample of \(\mathrm{CaCl}_{2}\) is dissolved in 125 g water, with both substances at \(25.0^{\circ} \mathrm{C}\) . Calculate the final temperature of the solution assuming no heat loss to the surroundings and assuming the solution has a specific heat capacity of 4.18 $\mathrm{J} /^{\prime} \mathrm{C} \cdot \mathrm{g} .$

The bomb calorimeter in Exercise 112 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_{\mathrm{comb}}=\right.\( \)-26.42 \mathrm{kJ} / \mathrm{g}$ ) is combusted in the calorimeter. What is the final temperature of the calorimeter contents?

How is average bond strength related to relative potential energies of the reactants and the products?

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