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: $$ \mathrm{Ag}^{+}(a q)+\mathrm{Cl}^{-}(a q) \longrightarrow \operatorname{AgCl}(s) $$ 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 \(4.18 \mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{g} .\)

Short Answer

Expert verified
The heat that accompanies the reaction of \(\mathrm{Ag}^{+}(a q)+\mathrm{Cl}^{-}(a q) \longrightarrow \operatorname{AgCl}(s)\) is 66.9 \(\mathrm{kJ} / \mathrm{mol}\) of \(\mathrm{AgCl}\) formed.

Step by step solution

01

Calculate the moles of AgCl formed

We are given that 50.0 mL of 0.100 M \(\mathrm{AgNO}_{3}\) solution is mixed with 50.0 mL of 0.100 M \(\mathrm{HCl}\) solution. The reaction is: $$ \mathrm{Ag}^{+}(a q)+\mathrm{Cl}^{-}(a q) \longrightarrow \operatorname{AgCl}(s) $$ Since the reaction has a 1:1 stoichiometry, the amounts of \(\mathrm{Ag}^{+}\) and \(\mathrm{Cl}^{-}\) that react are equal. So we can find the moles of \(\mathrm{AgCl}\) formed by finding the moles of either \(\mathrm{Ag}^{+}\) or \(\mathrm{Cl}^{-}\) in the initial solutions and taking the lowest amount as the limiting reagent. Moles of \(\mathrm{Ag}^{+}\) = Molarity × Volume = 0.100 mol/L × 0.0500 L = 0.00500 mol Moles of \(\mathrm{Cl}^{-}\) = Molarity × Volume = 0.100 mol/L × 0.0500 L = 0.00500 mol Both have equal moles, so either can be considered the limiting reagent. Thus, 0.00500 mol of \(\mathrm{AgCl}\) is formed.
02

Calculate the heat transferred

The two solutions are initially at 22.60 \(^\circ\mathrm{C}\) and finally reach a temperature of 23.40 \(^\circ\mathrm{C}\). The mass of the combined solution is 100.0 g, and its specific heat capacity is 4.18 \(\mathrm{~J} / { }^{\circ} \mathrm{C} \cdot \mathrm{g}\). To calculate the heat transferred, we will use the formula: q = mcΔT where: - q is the heat transferred - m is the mass of the combined solution (100.0 g) - c is the specific heat capacity (4.18 \(\mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{g}\)) - ΔT is the change in temperature (23.40 \(^\circ\mathrm{C}\) - 22.60 \(^\circ\mathrm{C}\)) q = (100.0 g) × (4.18 \(\mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{g}\)) × (23.40 \(^\circ\mathrm{C}\) - 22.60 \(^\circ\mathrm{C}\)) q = (100.0 g) × (4.18 \(\mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{g}\)) × (0.80 \(^\circ\mathrm{C}\)) q = 334.4 J
03

Calculate the heat per mole of AgCl

Now we have the total heat transferred (q) and the moles of \(\mathrm{AgCl}\) formed. To calculate the heat per mole of \(\mathrm{AgCl}\) formed, we will use the formula: Heat per mole of AgCl = \(\frac{q}{n}\) where: - q is the heat transferred (334.4 J) - n is the moles of \(\mathrm{AgCl}\) formed (0.00500 mol) Heat per mole of AgCl = \(\frac{334.4 \mathrm{~J}}{0.00500 \mathrm{~mol}}\) = 66880 J/mol Now we will convert the heat per mole of AgCl from J/mol to kJ/mol: 66880 J/mol × \(\frac{1 \mathrm{~kJ}}{1000 \mathrm{~J}}\) = 66.9 \(\mathrm{kJ} / \mathrm{mol}\) The heat that accompanies this reaction is 66.9 \(\mathrm{kJ} / \mathrm{mol}\) of \(\mathrm{AgCl}\) formed.

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Most popular questions from this chapter

In a coffee-cup calorimeter, \(100.0 \mathrm{~mL}\) of \(1.0 \mathrm{M} \mathrm{NaOH}\) and \(100.0 \mathrm{~mL}\) of \(1.0 \mathrm{M} \mathrm{HCl}\) are mixed. Both solutions were originally at \(24.6^{\circ} \mathrm{C}\). After the reaction, the final temperature is \(31.3^{\circ} \mathrm{C}\). Assuming that all the solutions have a density of \(1.0 \mathrm{~g} / \mathrm{cm}^{3}\) and a specific heat capacity of \(4.18 \mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{g}\), calcu- late the enthalpy change for the neutralization of \(\mathrm{HCl}\) by \(\mathrm{NaOH}\). Assume that no heat is lost to the surroundings or to the calorimeter.

In a bomb calorimeter, the reaction vessel is surrounded by water that must be added for each experiment. Since the amount of water is not constant from experiment to experiment, the mass of water must be measured in each case. The heat capacity of the calorimeter is broken down into two parts: the water and the calorimeter components. If a calorimeter contains \(1.00 \mathrm{~kg}\) water and has a total heat capacity of \(10.84 \mathrm{~kJ} /{ }^{\circ} \mathrm{C}\), what is the heat capacity of the calorimeter components?

The combustion of \(0.1584 \mathrm{~g}\) benzoic acid increases the temperature of a bomb calorimeter by \(2.54^{\circ} \mathrm{C}\). Calculate the heat capacity of this calorimeter. (The energy released by combustion of benzoic acid is \(26.42 \mathrm{~kJ} / \mathrm{g}\).) A \(0.2130\) -g sample of vanillin \(\left(\mathrm{C}_{8} \mathrm{H}_{8} \mathrm{O}_{3}\right)\) is then burned in the same calorimeter, and the temperature increases by \(3.25^{\circ} \mathrm{C}\). What is the energy of combustion per gram of vanillin? Per mole of vanillin?

The preparation of \(\mathrm{NO}_{2}(g)\) from \(\mathrm{N}_{2}(g)\) and \(\mathrm{O}_{2}(g)\) is an endothermic reaction: $$ \mathrm{N}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow \mathrm{NO}_{2}(g) \text { (unbalanced) } $$ The enthalpy change of reaction for the balanced equation (with lowest whole- number coefficients) is \(\Delta H=67.7 \mathrm{~kJ}\). If \(2.50 \times 10^{2} \mathrm{~mL} \mathrm{~N}_{2}(g)\) at \(100 .{ }^{\circ} \mathrm{C}\) and \(3.50 \mathrm{~atm}\) and \(4.50 \times\) \(10^{2} \mathrm{~mL} \mathrm{O}_{2}(g)\) at \(100 .{ }^{\circ} \mathrm{C}\) and \(3.50\) atm are mixed, what amount of heat is necessary to synthesize the maximum yield of \(\mathrm{NO}_{2}(g) ?\)

A balloon filled with \(39.1\) moles of helium has a volume of \(876 \mathrm{~L}\) at \(0.0^{\circ} \mathrm{C}\) and \(1.00\) atm pressure. The temperature of the balloon is increased to \(38.0^{\circ} \mathrm{C}\) as it expands to a volume of \(998 \mathrm{~L}\), the pressure remaining constant. Calculate \(q, w\), and \(\Delta E\) for the helium in the balloon. (The molar heat capacity for helium gas is \(20.8 \mathrm{~J} /{ }^{\circ} \mathrm{C} \cdot \mathrm{mol}\).)

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