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Introductory Chemistry - 1st Canadian Edition: Enthalpy and Chemical Reactions

Introductory Chemistry - 1st Canadian Edition
Enthalpy and Chemical Reactions
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table of contents
  1. Cover
  2. Title Page
  3. Copyright
  4. Table Of Contents
  5. Acknowledgments
  6. Dedication
  7. About BCcampus Open Education
  8. Chapter 1. What is Chemistry
    1. Some Basic Definitions
    2. Chemistry as a Science
  9. Chapter 2. Measurements
    1. Expressing Numbers
    2. Significant Figures
    3. Converting Units
    4. Other Units: Temperature and Density
    5. Expressing Units
    6. End-of-Chapter Material
  10. Chapter 3. Atoms, Molecules, and Ions
    1. Acids
    2. Ions and Ionic Compounds
    3. Masses of Atoms and Molecules
    4. Molecules and Chemical Nomenclature
    5. Atomic Theory
    6. End-of-Chapter Material
  11. Chapter 4. Chemical Reactions and Equations
    1. The Chemical Equation
    2. Types of Chemical Reactions: Single- and Double-Displacement Reactions
    3. Ionic Equations: A Closer Look
    4. Composition, Decomposition, and Combustion Reactions
    5. Oxidation-Reduction Reactions
    6. Neutralization Reactions
    7. End-of-Chapter Material
  12. Chapter 5. Stoichiometry and the Mole
    1. Stoichiometry
    2. The Mole
    3. Mole-Mass and Mass-Mass Calculations
    4. Limiting Reagents
    5. The Mole in Chemical Reactions
    6. Yields
    7. End-of-Chapter Material
  13. Chapter 6. Gases
    1. Pressure
    2. Gas Laws
    3. Other Gas Laws
    4. The Ideal Gas Law and Some Applications
    5. Gas Mixtures
    6. Kinetic Molecular Theory of Gases
    7. Molecular Effusion and Diffusion
    8. Real Gases
    9. End-of-Chapter Material
  14. Chapter 7. Energy and Chemistry
    1. Formation Reactions
    2. Energy
    3. Stoichiometry Calculations Using Enthalpy
    4. Enthalpy and Chemical Reactions
    5. Work and Heat
    6. Hess’s Law
    7. End-of-Chapter Material
  15. Chapter 8. Electronic Structure
    1. Light
    2. Quantum Numbers for Electrons
    3. Organization of Electrons in Atoms
    4. Electronic Structure and the Periodic Table
    5. Periodic Trends
    6. End-of-Chapter Material
  16. Chapter 9. Chemical Bonds
    1. Lewis Electron Dot Diagrams
    2. Electron Transfer: Ionic Bonds
    3. Covalent Bonds
    4. Other Aspects of Covalent Bonds
    5. Violations of the Octet Rule
    6. Molecular Shapes and Polarity
    7. Valence Bond Theory and Hybrid Orbitals
    8. Molecular Orbitals
    9. End-of-Chapter Material
  17. Chapter 10. Solids and Liquids
    1. Properties of Liquids
    2. Solids
    3. Phase Transitions: Melting, Boiling, and Subliming
    4. Intermolecular Forces
    5. End-of-Chapter Material
  18. Chapter 11. Solutions
    1. Colligative Properties of Solutions
    2. Concentrations as Conversion Factors
    3. Quantitative Units of Concentration
    4. Colligative Properties of Ionic Solutes
    5. Some Definitions
    6. Dilutions and Concentrations
    7. End-of-Chapter Material
  19. Chapter 12. Acids and Bases
    1. Acid-Base Titrations
    2. Strong and Weak Acids and Bases and Their Salts
    3. Brønsted-Lowry Acids and Bases
    4. Arrhenius Acids and Bases
    5. Autoionization of Water
    6. Buffers
    7. The pH Scale
    8. End-of-Chapter Material
  20. Chapter 13. Chemical Equilibrium
    1. Chemical Equilibrium
    2. The Equilibrium Constant
    3. Shifting Equilibria: Le Chatelier’s Principle
    4. Calculating Equilibrium Constant Values
    5. Some Special Types of Equilibria
    6. End-of-Chapter Material
  21. Chapter 14. Oxidation and Reduction
    1. Oxidation-Reduction Reactions
    2. Balancing Redox Reactions
    3. Applications of Redox Reactions: Voltaic Cells
    4. Electrolysis
    5. End-of-Chapter Material
  22. Chapter 15. Nuclear Chemistry
    1. Units of Radioactivity
    2. Uses of Radioactive Isotopes
    3. Half-Life
    4. Radioactivity
    5. Nuclear Energy
    6. End-of-Chapter Material
  23. Chapter 16. Organic Chemistry
    1. Hydrocarbons
    2. Branched Hydrocarbons
    3. Alkyl Halides and Alcohols
    4. Other Oxygen-Containing Functional Groups
    5. Other Functional Groups
    6. Polymers
    7. End-of-Chapter Material
  24. Chapter 17. Kinetics
    1. Factors that Affect the Rate of Reactions
    2. Reaction Rates
    3. Rate Laws
    4. Concentration–Time Relationships: Integrated Rate Laws
    5. Activation Energy and the Arrhenius Equation
    6. Reaction Mechanisms
    7. Catalysis
    8. End-of-Chapter Material
  25. Chapter 18. Chemical Thermodynamics
    1. Spontaneous Change
    2. Entropy and the Second Law of Thermodynamics
    3. Measuring Entropy and Entropy Changes
    4. Gibbs Free Energy
    5. Spontaneity: Free Energy and Temperature
    6. Free Energy under Nonstandard Conditions
    7. End-of-Chapter Material
  26. Appendix A: Periodic Table of the Elements
  27. Appendix B: Selected Acid Dissociation Constants at 25°C
  28. Appendix C: Solubility Constants for Compounds at 25°C
  29. Appendix D: Standard Thermodynamic Quantities for Chemical Substances at 25°C
  30. Appendix E: Standard Reduction Potentials by Value
  31. Glossary
  32. About the Authors
  33. Versioning History

Enthalpy and Chemical Reactions

Learning Objectives

  1. Define enthalpy.
  2. Properly express the enthalpy change of chemical reactions.
  3. Explain how enthalpy changes are measured experimentally.

Now that we have shown how energy, work, and heat are related, we are ready to consider energy changes in chemical reactions. A fundamental concept is that every chemical reaction occurs with a concurrent change in energy. Now we need to learn how to properly express these energy changes.

Our study of gases in Chapter 6 “Gases” and our definition of work in the section “Work and Heat” indicate that conditions like pressure, volume, and temperature affect the energy content of a system. What we need is a definition of energy that holds when some of these conditions are specified (somewhat similar to our definition of standard temperature and pressure in our study of gases). We define the enthalpy change (ΔH) as the heat of a process when pressure is held constant:

\Delta H \equiv q\text{ at constant pressure}

The letter H stands for “enthalpy,” a kind of energy, while the Δ implies a change in the quantity. We will always be interested in the change in H, rather than the absolute value of H itself.

When a chemical reaction occurs, there is a characteristic change in enthalpy. The enthalpy change for a reaction is typically written after a balanced chemical equation and on the same line. For example, when two moles of hydrogen react with one mole of oxygen to make two moles of water, the characteristic enthalpy change is 570 kJ. We write the equation as:

\ce{2H2(g)}+\ce{O2(g)}\rightarrow\ce{2H2O(\ell)}\quad \Delta H=-570\text{ kJ}

A chemical equation that includes an enthalpy change is called a thermochemical equation. A thermochemical equation is assumed to refer to the equation in molar quantities, which means it must be interpreted in terms of moles, not individual molecules.

Example 7.8

Problem

Write the thermochemical equation for the reaction of PCl3(g) with Cl2(g) to make PCl5(g), which has an enthalpy change of −88 kJ.

Solution

\ce{PCl3(g)}+\ce{Cl2(g)}\rightarrow \ce{PCl5(g)}\quad \Delta H=-88\text{ kJ}

Test Yourself

Write the thermochemical equation for the reaction of N2(g) with O2(g) to make 2NO(g), which has an enthalpy change of 181 kJ.

Answer

\ce{N2(g)}+\ce{O2(g)}\rightarrow \ce{2NO(g)}\quad \Delta H = 181\text{ kJ}

You may have noticed that the ΔH for a chemical reaction may be positive or negative. The number is assumed to be positive if it has no sign; a + sign can be added explicitly to avoid confusion. A chemical reaction that has a positive ΔH is said to be endothermic, while a chemical reaction that has a negative ΔH is said to be exothermic.

What does it mean if the ΔH of a process is positive? It means that the system in which the chemical reaction is occurring is gaining energy. If one considers the energy of a system as being represented as a height on a vertical energy plot, the enthalpy change that accompanies the reaction can be diagrammed as in part (a) in Figure 7.3 “Reaction Energy”: the energy of the reactants has some energy, and the system increases its energy as it goes to products. The products are higher on the vertical scale than the reactants. Endothermic, then, implies that the system gains, or absorbs, energy.

An opposite situation exists for an exothermic process, as shown in part (b) in Figure 7.3 “Reaction Energy.” If the enthalpy change of a reaction is negative, the system is losing energy, so the products have less energy than the reactants, and the products are lower on the vertical energy scale than the reactants are. Exothermic, then, implies that the system loses, or gives off, energy.

Figure 7.3 “Reaction Energy.” Part (a): In an endothermic reaction, the energy of the system increases (i.e., moves higher on the vertical scale of energy). Part (b): In an exothermic reaction, the energy of the system decreases (i.e., moves lower on the vertical scale of energy).

Example 7.9

Problem

Consider this thermochemical equation:

\ce{2CO(g)}+\ce{O2(g)}\rightarrow \ce{2CO2(g)}}\quad \Delta H=-565\text{ kJ}

Is it exothermic or endothermic? How much energy is given off or absorbed?

Solution

By definition, a chemical reaction that has a negative ΔH is exothermic, meaning that this much energy — in this case, 565 kJ — is given off by the reaction.

Test Yourself

Consider this thermochemical equation:

\ce{CO2(g)}+\ce{H2(g)}\rightarrow \ce{CO(g)}+\ce{H2O(g)}\quad \Delta H=42\text{ kJ}

Is it exothermic or endothermic? How much energy is given off or absorbed?

Answer

Endothermic; 42 kJ are absorbed.

How are ΔH values measured experimentally? Actually, ΔH is not measured; q is measured. But the measurements are performed under conditions of constant pressure, so ΔH is equal to the q measured.

Experimentally, q is measured by taking advantage of the following equation:

q=mc\Delta T

We premeasure the mass of the chemicals in a system. Then we let the chemical reaction occur and measure the change in temperature (ΔT) of the system. If we know the specific heat of the materials in the system (typically, we do), we can calculate q. That value of q is numerically equal to the ΔH of the process, which we can scale up to a molar scale. The container in which the system resides is typically insulated, so any energy change goes into changing the temperature of the system, rather than being leaked from the system. The container is referred to as a calorimeter, and the process of measuring changes in enthalpy is called calorimetry.

A thermometer and a stirrer stick out of the cover of some nested coffee cups.
Figure 7.4 “Calorimeter.” A simple calorimeter can be constructed from some nested foam coffee cups, a cover, a thermometer, and a stirrer.

For example, suppose 4.0 g of NaOH, or 0.10 mol of NaOH, are dissolved to make 100.0 mL of aqueous solution, while 3.65 g of HCl, or 0.10 mol of HCl, are dissolved to make another 100.0 mL of aqueous solution. The two solutions are mixed in an insulated calorimeter, a thermometer is inserted, and the calorimeter is covered (see Figure 7.4 “Calorimeter” for an example setup). The thermometer measures the temperature change as the following chemical reaction occurs:

\ce{NaOH(aq)}+\ce{HCl(aq)}\rightarrow \ce{NaCl(aq)}+\ce{H2O(\ell)}

An observer notes that the temperature increases from 22.4°C to 29.1°C. Assuming that the heat capacities and densities of the solutions are the same as those of pure water, we now have the information we need to determine the enthalpy change of the chemical reaction. The total amount of solution is 200.0 mL, and with a density of 1.00 g/mL, we thus have 200.0 g of solution. Using the equation for q, we substitute for our experimental measurements and the specific heat of water (see Table 7.1 “Enthalpies of Formation for Various Substances” in “Formation Reactions”):

q=(200.0\text{ \cancel{g}})\left(4.184\cdot \dfrac{\text{J}}{\cancel{\text{g}}\cdot \cancel{\degree\text{C}}}\right)(6.7\text{ }\cancel{\degree\text{C}})

Solving for q, we get:

q=5,600\text{ J}\equiv \Delta H\text{ for the reaction}

The heat q is equal to the ΔH for the reaction because the chemical reaction occurs at constant pressure. However, the reaction is giving off this amount of energy, so the actual sign on ΔH is negative:

\Delta H=-5,600\text{ J for the reaction}

Thus, we have the following thermochemical equation for the chemical reaction that occurred in the calorimeter:

\ce{\dfrac{1}{10}NaOH(aq)}+\ce{\dfrac{1}{10}HCl(aq)}\rightarrow \ce{\dfrac{1}{10}NaCl(aq)}+\ce{\dfrac{1}{10}H2O(\ell)}\quad \Delta H=-5,600\text{ J}

The \frac{1}{10} coefficients are present to remind us that we started with one-tenth of a mole of each reactant, so we make one-tenth of a mole of each product. Typically, however, we report thermochemical equations in terms of moles, not one-tenth of a mole. To scale up to molar quantities, we must multiply the coefficients by 10. However, when we do this, we get 10 times as much energy. Thus, we have:

\ce{NaOH(aq)}+\ce{HCl(aq)}\rightarrow \ce{NaCl(aq)}+\ce{H2O(\ell)}\quad \Delta H=-56,000\text{ J}

The ΔH can be converted into kJ units, so our final thermochemical equation is:

\ce{NaOH(aq)}+\ce{HCl(aq)}\rightarrow \ce{NaCl(aq)}+\ce{H2O(\ell)}\quad \Delta H=-56\text{ kJ}

We have just taken our experimental data from calorimetry and determined the enthalpy change of a chemical reaction. Similar measurements on other chemical reactions can determine the ΔH values of any chemical reaction you want to study.

Example 7.10

Problem

A 100 mL solution of 0.25 mol of Ca2+(aq) was mixed with 0.50 mol of F−(aq) ions, and CaF2 was precipitated:

\ce{Ca^{2+}(aq)}+\ce{2F^{-}(aq)}\rightarrow\ce{CaF2(s)}

The temperature of the solution increased by 10.5°C. What was the enthalpy change for the chemical reaction? What was the enthalpy change for the production of 1 mol of CaF2? Assume that the solution has the same density and specific heat as water.

Solution

Because we are given ΔT directly, we can determine the heat of the reaction, which is equal to ΔH:

q=(100\text{ \cancel{g}})\left(4.184\cdot \dfrac{\text{J}}{\cancel{\text{g}}\cdot \cancel{\degree\text{C}}}\right)(10.5\text{ }\cancel{\degree\text{C}})

Solving for q, we get:

q=4,400\text{ J}

Therefore, ΔH = −4,400 J.

According to the stoichiometry of the reaction, exactly 0.25 mol of CaF2 will form, so this quantity of heat is for 0.25 mol. For 1 mol of CaF2, we need to scale up the heat by a factor of four:

q=4,400\text{ J}\times 4=17,600\text{ J for 1 mol }\ce{CaF2}

On a molar basis, the change in enthalpy is:

\Delta H=-17,600\text{ J}=-17.6\text{ kJ}

Test Yourself

In a calorimeter at constant pressure, 0.10 mol of CH4(g) and 0.20 mol of O2(g) are reacted, according to the following equation:

\ce{CH4(g)}+\ce{2O2(g)}\rightarrow \ce{CO2(g)}+\ce{2H2O(\ell)}

The reaction warms 750.0 g of H2O by 28.4°C. What is ΔH for the reaction on a molar scale?

Answer

−891 kJ

Key Takeaways

  • Every chemical reaction occurs with a concurrent change in energy.
  • The change in enthalpy equals heat at constant pressure.
  • Enthalpy changes can be expressed by using thermochemical equations.
  • Enthalpy changes are measured by using calorimetry.

Exercises

Questions

  1. Under what circumstances are q and ΔH the same?
  2. Under what circumstances are q and ΔH different?
  3. Hydrogen gas and chlorine gas react to make hydrogen chloride gas with an accompanying enthalpy change of −184 kJ. Write a properly balanced thermochemical equation for this process.
  4. Propane (C3H8) reacts with elemental oxygen gas to produce carbon dioxide and liquid water with an accompanying enthalpy change of −2,220 kJ. Write a properly balanced thermochemical equation for this process.
  5. Nitrogen gas reacts with oxygen gas to make NO(g) while absorbing 180 kJ. Write a properly balanced thermochemical equation for this process.
  6. Solid sodium reacts with chlorine gas to make solid sodium chloride while giving off 772 kJ. Write a properly balanced thermochemical equation for this process.
  7. Hydrogen gas and chlorine gas react to make hydrogen chloride gas with an accompanying enthalpy change of −184 kJ. Is this process endothermic or exothermic?
  8. Propane (C3H8) reacts with elemental oxygen gas to produce carbon dioxide while giving off 2,220 kJ of energy. Is this process endothermic or exothermic?
  9. Nitrogen gas reacts with oxygen gas to make NO(g) while absorbing 180 kJ. Is this process exothermic or endothermic?
  10. Sodium metal can react with nitrogen to make sodium azide (NaN3) with a ΔH of 21.72 kJ. Is this process exothermic or endothermic?
  11. Draw an energy level diagram for the chemical reaction in Exercise 8. (See Figure 7.3 “Reaction Energy” for an example.)
  12. Draw an energy level diagram for the chemical reaction in Exercise 9. (See Figure 7.3 “Reaction Energy” for an example.)
  13. In a 250 mL solution, 0.25 mol of KOH(aq) and 0.25 mol of HNO3(aq) are combined. The temperature of the solution increases from 22.5°C to 35.9°C. Assume the solution has the same density and heat capacity of water. What is the heat of the reaction, and what is the ΔH of the reaction on a molar basis?
  14. In a 600 mL solution, 0.50 mol of Ca(OH)2(aq) and 0.50 mol of H2SO4(aq) are combined. The temperature of the solution increases by 22.3°C. What is the heat of the reaction, and what is the ΔH of the reaction on a molar basis? Assume the solution has the same density and heat capacity of water.
  15. To warm 400.0 g of H2O, 0.050 mol of ethanol (C2H5OH) is burned. The water warms from 24.6°C to 65.6°C. What is the heat of the reaction, and what is the ΔH of the reaction on a molar basis?
  16. To warm 100.0 g of H2O, 0.066 mol beeswax is burned. The water warms from 21.4°C to 25.5°C. What is the heat of the reaction, and what is the ΔH of the reaction on a molar basis?

Answers

  1. under conditions of constant pressure
  1. \ce{H2(g)}+\ce{Cl2(g)}\rightarrow\ce{2HCl(g)}\quad \Delta H=-184\text{ kJ}
  1. \ce{N2(g)}+\ce{O2(g)}\rightarrow \ce{2NO(g)}\quad \Delta H=180\text{ kJ}
  1. exothermic
  1. endothermic
  1. \setlength{\unitlength}{1cm} \thicklines \begin{picture}(7,6)(0,0) \put(-2,3){Energy} \put(0,0){\line(0,6){5}} \put(0,0){\line(11,0){10.5}} \put(0.5,4){\line(4,0){4}} \put(0.5,4.2){\ce{C3H8}+\ce{5O2}} \put(4.5,4){\vector(1,-1){3}} \put(7.5,1){\line(3,0){3}} \put(6,2.75){2200 kJ emitted} \put(7.6,1.2){\ce{3CO2}+\ce{4H2O}} \end{picture}
  1. heat of reaction = −14.0 kJ; ΔH = −56.0 kJ/mol of reactants
  1. heat of reaction = −68.6 kJ; ΔH = −1,370 kJ/mole of ethanol

Media Attributions

  • “Reaction Energy” by David W. Ball © CC BY-NC-SA (Attribution-NonCommercial-ShareAlike)
  • “Calorimeter” by David W. Ball © CC BY-NC-SA (Attribution-NonCommercial-ShareAlike)

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Copyright © 2014

                                by Jessie A. Key

            Introductory Chemistry - 1st Canadian Edition by Jessie A. Key is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, except where otherwise noted.
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