Given the following data $$\mathrm{Ca}(s)+2 \mathrm{C}(\text { graphite }) \longrightarrow \mathrm{CaC}_{2}(s)$$ \(\Delta H=-62.8 \mathrm{kJ}\) $$ \mathrm{Ca}(s)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{CaO}(s) $$ \(\Delta H=-635.5 \mathrm{kJ}\) $$ \mathrm{CaO}(s)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{Ca}(\mathrm{OH})_{2}(a q) $$ \(\Delta H=-653.1 \mathrm{kJ}\) $$ \mathrm{C}_{2} \mathrm{H}_{2}(g)+\frac{5}{2} \mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{CO}_{2}(g)+\mathrm{H}_{2} \mathrm{O}(l) $$ \(\Delta H=-1300 . \mathrm{kJ}\) $$ \mathrm{C}(\text {graphite})+\mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(\mathrm{g}) $$ \(\Delta H=-393.5 \mathrm{kJ}\) calculate \(\Delta H\) for the reaction $$ \mathrm{CaC}_{2}(s)+2 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{Ca}(\mathrm{OH})_{2}(a q)+\mathrm{C}_{2} \mathrm{H}_{2}(g) $$

Short Answer

Expert verified
The enthalpy change, ∆H, for the target reaction \(\mathrm{CaC}_{2}(s) + 2 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{Ca}(\mathrm{OH})_{2}(a q)+\mathrm{C}_{2} \mathrm{H}_{2}(g)\) is \(-1799.9\,\mathrm{kJ}\).

Step by step solution

01

Identify the target reaction

The target reaction is $$ \mathrm{CaC}_{2}(s)+2 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{Ca}(\mathrm{OH})_{2}(a q)+\mathrm{C}_{2} \mathrm{H}_{2}(g) $$ Our goal is to find its enthalpy change, ∆H.
02

Manipulate the given reactions using Hess's Law

We need to manipulate the given reactions in such a way that they will sum up to the target reaction. The most straightforward way we can do that is to find a way for the given reactions to cancel out as many compounds as possible while resulting in the target reaction. Here's how we can manipulate them: 1. Reverse the first reaction and double the second and fifth reaction to obtain the correct coefficients for the target reaction: $$\mathrm{CaC}_{2(s)} \longrightarrow \mathrm{Ca(s)} + 2 \mathrm{C(graphite)}$$ \(\Delta H = 62.8\,\mathrm{kJ}\) (reversed) $$2(\mathrm{Ca}(s)+\frac{1}{2} \mathrm{O}_{2}(g) \longrightarrow \mathrm{CaO}(s))$$ \(2 \Delta H = 2(-635.5)\,\mathrm{kJ}\) (multiplied by 2) $$2(\mathrm{C}(\text {graphite})+\mathrm{O}_{2}(g) \longrightarrow \mathrm{CO}_{2}(\mathrm(g)))$$ \(2 \Delta H = 2(-393.5)\,\mathrm{kJ}\) (multiplied by 2) 2. Add the third and fourth reaction as they are: $$\mathrm{CaO}(s)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{Ca}(\mathrm{OH})_{2}(a q)$$ \(\Delta H = -653.1\,\mathrm{kJ}\) $$\mathrm{C}_{2} \mathrm{H}_{2}(g)+\frac{5}{2} \mathrm{O}_{2}(g) \longrightarrow 2\mathrm{CO}_{2}(g)+\mathrm{H}_{2} \mathrm{O}(l)$$ \(\Delta H = -1300\,\mathrm{kJ}\)
03

Combine the manipulated reactions

Now, sum up the manipulated reactions. The intermediate compounds will cancel out, resulting in the target reaction: $$ \mathrm{CaC}_{2}(s) + 2 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{Ca}(\mathrm{OH})_{2}(a q)+\mathrm{C}_{2} \mathrm{H}_{2}(g) $$
04

Calculate the enthalpy change of the target reaction

Add the enthalpies change (∆H) of the manipulated reactions to find the ∆H of the target reaction: $$\Delta H_\text{target} = 62.8\,\mathrm{kJ} + 2(-635.5)\,\mathrm{kJ} + 2(-393.5)\,\mathrm{kJ} - 653.1\,\mathrm{kJ} - 1300\,\mathrm{kJ}$$ $$\Delta H_\text{target} = -1799.9\,\mathrm{kJ}$$ So the enthalpy change, ∆H, for the target reaction is -1799.9 kJ.

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Most popular questions from this chapter

For the process $\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{H}_{2} \mathrm{O}(g)\( at 298 \)\mathrm{K}\( and \)1.0 \mathrm{atm},\( \)\Delta H$ is more positive than \(\Delta E\) by 2.5 \(\mathrm{kJ} / \mathrm{mol}\) . What does the 2.5 \(\mathrm{kJ} / \mathrm{mol}\) quantity represent?

A serving size of six cookies contains 4 g of fat, 20 of carbohydrates, and 2 g of protein. If walking 1.0 mile consumes 170 kJ of energy, how many miles must you walk to burn off enough calories to eat six cookies? Assume the energy content of fats, carbohydrates, and proteins are 8 kcallg, 4 kcallg, and 4 kcallg, respectively.

Consider the reaction $$ 2 \mathrm{HCl}(a q)+\mathrm{Ba}(\mathrm{OH})_{2}(a q) \longrightarrow \mathrm{BaCl}_{2}(a q)+2 \mathrm{H}_{2} \mathrm{O}(l) $$ $$ \Delta H=-118 \mathrm{kJ} $$ Calculate the heat when 100.0 \(\mathrm{mL}\) of 0.500\(M \mathrm{HCl}\) is mixed with 300.0 \(\mathrm{mL}\) of 0.100\(M \mathrm{Ba}(\mathrm{OH})_{2}\) . Assuming that the temperature of both solutions was initially \(25.0^{\circ} \mathrm{C}\) and that the final mixture has a mass of 400.0 \(\mathrm{g}\) and a specific heat capacity of 4.18 \(\mathrm{J} / \mathrm{C} \cdot \mathrm{g}\) , calculate the final temperature of the mixture.

In a coffee-cup calorimeter, 150.0 \(\mathrm{mL}\) of 0.50 \(\mathrm{M}\) HCl is added to 50.0 \(\mathrm{mL}\) of 1.00 \(\mathrm{M} \mathrm{NaOH}\) to make 200.0 \(\mathrm{g}\) solution at an initial temperature of \(48.2^{\circ} \mathrm{C}\) . If the enthalpy of neutralization for the reaction between a strong acid and a strong base is \(-56 \mathrm{kJ} / \mathrm{mol}\) , calculate the final temperature of the calorimeter contents. Assume the specific heat capacity of the solution is 4.184 \(\mathrm{J} /^{\circ} \mathrm{C} \cdot \mathrm{g}\) and assume no heat loss to the surroundings.

The reaction $$ \mathrm{SO}_{3}(g)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow \mathrm{H}_{2} \mathrm{SO}_{4}(a q) $$ is the last step in the commercial production of sulfuric acid. The enthalpy change for this reaction is \(-227 \mathrm{kJ} .\) In designing a sulfuric acid plant, is it necessary to provide for heating or cooling of the reaction mixture? Explain.

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