Chapter 7: Problem 50
Compressed air in aerosol cans is used to free electronic equipment of dust. Does the air do any work as it escapes from the can?
Chapter 7: Problem 50
Compressed air in aerosol cans is used to free electronic equipment of dust. Does the air do any work as it escapes from the can?
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Get started for freeA \(1.00 \mathrm{g}\) sample of \(\mathrm{Ne}(\mathrm{g})\) at 1 atm pressure and \(27^{\circ} \mathrm{C}\) is allowed to expand into an evacuated vessel of \(2.50 \mathrm{L}\) volume. Does the gas do work? Explain.
A sample gives off 5228 cal when burned in a bomb calorimeter. The temperature of the calorimeter assembly increases by \(4.39^{\circ} \mathrm{C} .\) Calculate the heat capacity of the calorimeter, in kilojoules per degree Celsius.
In a student experiment to confirm Hess's law, the reaction $$\mathrm{NH}_{3}(\text { concd aq })+\mathrm{HCl}(\mathrm{aq}) \longrightarrow \mathrm{NH}_{4} \mathrm{Cl}(\mathrm{aq})$$ was carried out in two different ways. First, \(8.00 \mathrm{mL}\) of concentrated \(\mathrm{NH}_{3}(\text { aq })\) was added to \(100.0 \mathrm{mL}\) of 1.00 M HCl in a calorimeter. [The NH \(_{3}(\) aq) was slightly in excess.] The reactants were initially at \(23.8^{\circ} \mathrm{C},\) and the final temperature after neutralization was \(35.8^{\circ} \mathrm{C} .\) In the second experiment, air was bubbled through \(100.0 \mathrm{mL}\) of concentrated \(\mathrm{NH}_{3}(\mathrm{aq})\) sweeping out \(\mathrm{NH}_{3}(\mathrm{g})\) (see sketch). The \(\mathrm{NH}_{3}(\mathrm{g})\) was neutralized in \(100.0 \mathrm{mL}\) of \(1.00 \mathrm{M} \mathrm{HCl}\). The temperature of the concentrated \(\mathrm{NH}_{3}(\text { aq })\) fell from 19.3 to \(13.2^{\circ} \mathrm{C} .\) At the same time, the temperature of the 1.00 M HCl rose from 23.8 to 42.9 ^ C as it was neutralized by \(\mathrm{NH}_{3}(\mathrm{g}) .\) Assume that all solutions have densities of \(1.00 \mathrm{g} / \mathrm{mL}\) and specific heats of \(4.18 \mathrm{Jg}^{-1 \circ} \mathrm{C}^{-1}\) (a) Write the two equations and \(\Delta H\) values for the processes occurring in the second experiment. Show that the sum of these two equations is the same as the equation for the reaction in the first experiment. (b) Show that, within the limits of experimental error, \(\Delta H\) for the overall reaction is the same in the two experiments, thereby confirming Hess's law.
A \(7.26 \mathrm{kg}\) shot (as used in the sporting event, the shot put) is dropped from the top of a building \(168 \mathrm{m}\) high. What is the maximum temperature increase that could occur in the shot? Assume a specific heat of \(0.47 \mathrm{Jg}^{-1}\) \(^{\circ} \mathrm{C}^{-1}\) for the shot. Why would the actual measured temperature increase likely be less than the calculated value?
Under the entry \(\mathrm{H}_{2} \mathrm{SO}_{4},\) a reference source lists many values for the standard enthalpy of formation. For example, for pure \(\mathrm{H}_{2} \mathrm{SO}_{4}(1), \Delta H_{\mathrm{f}}^{\circ}=-814.0 \mathrm{kJ} / \mathrm{mol}\) for a solution with \(1 \mathrm{mol} \mathrm{H}_{2} \mathrm{O}\) per mole of \(\mathrm{H}_{2} \mathrm{SO}_{4}\) \(-841.8 ;\) with \(10 \mathrm{mol} \mathrm{H}_{2} \mathrm{O},-880.5 ;\) with \(50 \mathrm{mol} \mathrm{H}_{2} \mathrm{O}\) \(-886.8 ;\) with \(100 \mathrm{mol} \mathrm{H}_{2} \mathrm{O},-887.7 ;\) with \(500 \mathrm{mol} \mathrm{H}_{2} \mathrm{O}\) \(-890.5 ;\) with \(1000 \mathrm{mol} \mathrm{H}_{2} \mathrm{O},-892.3 ;\) with \(10,000 \mathrm{mol}\) \(\mathrm{H}_{2} \mathrm{O},-900.8 ;\) and with \(100,000 \mathrm{mol} \mathrm{H}_{2} \mathrm{O},-907.3\) (a) Explain why these values are not all the same. (b) The value of \(\Delta H_{\mathrm{f}}^{\circ}\left[\mathrm{H}_{2} \mathrm{SO}_{4}(\mathrm{aq})\right]\) in an infinitely dilute solution is \(-909.3 \mathrm{kJ} / \mathrm{mol} .\) What data from this chapter can you cite to confirm this value? Explain. (c) If \(500.0 \mathrm{mL}\) of \(1.00 \mathrm{M} \mathrm{H}_{2} \mathrm{SO}_{4}(\mathrm{aq})\) is prepared from pure \(\mathrm{H}_{2} \mathrm{SO}_{4}(1),\) what is the approximate change in temperature that should be observed? Assume that the \(\mathrm{H}_{2} \mathrm{SO}_{4}(1)\) and \(\mathrm{H}_{2} \mathrm{O}(1)\) are at the same temperature initially and that the specific heat of the \(\mathrm{H}_{2} \mathrm{SO}_{4}(\mathrm{aq})\) is about \(4.2 \mathrm{Jg}^{-1}\) \(^{\circ} \mathrm{C}^{-1}\).
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