Chapter 6: Problem 18
The enthalpy change for a reaction is a state function and it is an extensive property. Explain.
Chapter 6: Problem 18
The enthalpy change for a reaction is a state function and it is an extensive property. Explain.
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Get started for freeA \(5.00-\mathrm{g}\) sample of aluminum pellets (specific heat capacity \(=\) \(0.89 \mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{g}\) ) and a \(10.00-\mathrm{g}\) sample of iron pellets (specific heat capacity \(=0.45 \mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{g}\) ) are heated to \(100.0^{\circ} \mathrm{C}\). The mixture of hot iron and aluminum is then dropped into \(97.3 \mathrm{~g}\) water at \(22.0^{\circ} \mathrm{C}\). Calculate the final temperature of the metal and water mixture, assuming no heat loss to the surroundings.
For the reaction \(\mathrm{HgO}(s) \rightarrow \mathrm{Hg}(l)+\frac{1}{2} \mathrm{O}_{2}(g), \Delta H=+90.7 \mathrm{~kJ}:\) a. What quantity of heat is required to produce \(1 \mathrm{~mol}\) of mercury by this reaction? b. What quantity of heat is required to produce \(1 \mathrm{~mol}\) of oxygen gas by this reaction? c. What quantity of heat would be released in the following reaction as written? $$ 2 \mathrm{Hg}(l)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{HgO}(s) $$
In a coffee-cup calorimeter, \(50.0 \mathrm{~mL}\) of \(0.100 \mathrm{M} \mathrm{AgNO}_{3}\) 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 reaction in \(\mathrm{kJ} / \mathrm{mol}\) of \(\mathrm{AgCl}\) formed. Assume that the combined solution has a mass of \(100.0 \mathrm{~g}\) and a specific heat capacity of \(4.18 \mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{g}\).
The standard enthalpy of formation of \(\mathrm{H}_{2} \mathrm{O}(l)\) at \(298 \mathrm{~K}\) is \(-285.8\) \(\mathrm{kJ} / \mathrm{mol} .\) Calculate the change in internal energy for the following process at \(298 \mathrm{~K}\) and 1 atm: $$ \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{H}_{2}(g)+\frac{1}{2} \mathrm{O}_{2}(g) \quad \Delta E^{\circ}=? $$ (Hint: Using the ideal gas equation, derive an expression for work in terms of \(n, R\), and \(T\).)
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.
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