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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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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Enthalpy Change
Enthalpy change (\( \Delta H \)) is a fundamental concept in thermodynamics, especially when analyzing chemical reactions. It represents the heat absorbed or released during a chemical reaction at constant pressure. Whether a reaction absorbs or releases heat determines if it is endothermic or exothermic:
  • Endothermic Reaction: Absorbs heat from the surroundings, resulting in a positive enthalpy change.
  • Exothermic Reaction: Releases heat to the surroundings, resulting in a negative enthalpy change.
For the given problem, we are interested in finding the enthalpy change for a specific reaction. Using Hess's Law, we can determine the overall enthalpy change by manipulating and summing the enthalpy changes of a series of reactions. This allows us to indirectly calculate the energy change of a reaction that may be difficult to measure directly.

Always remember that the conservation of energy principle applies, meaning total energy remains constant. Therefore, even if individual reactions vary in their heat exchanges, their combined action results in the precise energy change needed for the target reaction.
Chemical Reactions
Chemical reactions involve the transformation of one or more substances into different substances. This transformation involves the breaking and forming of chemical bonds, and it is always accompanied by a flow of energy. When analyzing a chemical reaction:
  • The reactants are the starting materials.
  • The products are the substances formed as a result of the reaction.
The given exercise involves several reactions, each with its specific reactants and products. The target reaction formation requires a meticulous adjustment of individual reactions to achieve the desired end result using Hess's Law. Part of the skill in chemistry is recognizing how these reactions can be manipulated through reversing, multiplying, or adding to align with your goal.

Understanding these reactions in terms of their physical states and heat exchanges is pivotal in determining how energy flows and how the reactions interact with each other. In essence, mastering how to piece together given reactions to form a target reaction using Hess's Law is a critical skill for problem-solving in chemistry.
Calorimetry
Calorimetry is the science of measuring the amount of heat exchanged in chemical reactions or physical changes. It is a vital tool for understanding energy changes and determining the enthalpy change of reactions. During a calorimetric process:
  • A sample undergoing the change is enclosed in a calorimeter.
  • The heat absorbed or released by the reaction causes a temperature change in the surrounding medium.
The exercise here is essentially a theoretical application of the principles used in calorimetry to find the enthalpy change of a reaction. Although a calorimeter isn't physically involved, the mathematical manipulation of reactions functionally serves the same purpose.

Effective application of calorimetry requires consideration of several factors, including the specific heat of substances involved and the careful balancing of equation elements to ensure accuracy in calculated energy changes. Thus, even theoretical calorimetry exercises emphasize the importance of precision in calculating and interpreting energy changes in chemical processes.

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Most popular questions from this chapter

A swimming pool, 10.0 \(\mathrm{m}\) by \(4.0 \mathrm{m},\) is filled with water to a depth of 3.0 \(\mathrm{m}\) at a temperature of \(20.2^{\circ} \mathrm{C}\) . How much energy is required to raise the temperature of the water to \(24.6^{\circ} \mathrm{C} ?\)

Calculate \(\Delta E\) for each of the following. a. \(q=-47 \mathrm{kJ}, w=+88 \mathrm{kJ}\) b. \(q=+82 \mathrm{kJ}, w=-47 \mathrm{kJ}\) c. \(q=+47 \mathrm{kJ}, w=0\) d. In which of these cases do the surroundings do work on the system?

Quinone is an important type of molecule that is involved in photosynthesis. The transport of electrons mediated by quinone in certain enzymes allows plants to take water, carbon dioxide, and the energy of sunlight to create glucose. A 0.1964 -g sample of quinone \(\left(\mathrm{C}_{6} \mathrm{H}_{4} \mathrm{O}_{2}\right)\) is burned in a bomb calorimeter with a heat capacity of 1.56 \(\mathrm{kJ} / \mathrm{C}\) . The temperature of the calorimeter increases by \(3.2^{\circ} \mathrm{C}\) . Calculate the energy of combustion of quinone per gram and per mole.

The specific heat capacity of silver is 0.24 \(\mathrm{J} /^{\circ} \mathrm{C} \cdot \mathrm{g}\) a. Calculate the energy required to raise the temperature of 150.0 g Ag from 273 \(\mathrm{K}\) to 298 \(\mathrm{K}\) . b. Calculate the energy required to raise the temperature of 1.0 mole of \(\mathrm{Ag}\) by \(1.0^{\circ} \mathrm{C}\) (called the molar heat capacity of silver). c. It takes 1.25 \(\mathrm{kJ}\) of energy to heat a sample of pure silver from \(12.0^{\circ} \mathrm{C}\) to \(15.2^{\circ} \mathrm{C}\) . Calculate the mass of the sample of silver.

Consider the reaction $$ \mathrm{B}_{2} \mathrm{H}_{6}(g)+3 \mathrm{O}_{2}(g) \longrightarrow \mathrm{B}_{2} \mathrm{O}_{3}(s)+3 \mathrm{H}_{2} \mathrm{O}(g) \quad \Delta H=-2035 \mathrm{kJ} $$ Calculate the amount of heat released when 54.0 \(\mathrm{g}\) of diborane is combusted.

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