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Lesson Starter

Section 1 The Nature of Chemical Equilibrium. Chapter 18. Lesson Starter. List two everyday processes that can easily be reversed and two that cannot. The freezing of water and the melting of ice can be reversed The cooking of an egg or the lighting of a match cannot be reversed.

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Lesson Starter

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  1. Section 1 The Nature of Chemical Equilibrium Chapter 18 Lesson Starter • List two everyday processes that can easily be reversed and two that cannot. • The freezing of water and the melting of ice can be reversed • The cooking of an egg or the lighting of a match cannot be reversed. • For the reversible processes, describe the conditions that favor the process going in a particular direction. • Low temperature favors freezing, and high temperature favors melting.

  2. Section 1 The Nature of Chemical Equilibrium Chapter 18 Reversible Reactions • Theoretically, every reaction can proceed in two directions, forward and reverse. • Essentially all chemical reactions are considered to be reversible under suitable conditions. • A chemical reaction in which the products can react to re-form the reactants is called areversible reaction.

  3. Section 1 The Nature of Chemical Equilibrium Chapter 18 Reversible Reactions, continued • A reversible chemical reaction is in chemical equilibriumwhen the rate of its forward reaction equals the rate of its reverse reaction and the concentrations of its products and reactants remain unchanged. • A a state of dynamic equilibrium has been reached when the amounts of products and reactants remain constant. • Both reactions continue, but there is no net • change in the composition of the system.

  4. Section 1 The Nature of Chemical Equilibrium Chapter 18 Reversible Reactions, continued • The chemical equation for the reaction at equilibrium is written using double arrows to indicate the overall reversibility of the reaction.

  5. Section 1 The Nature of Chemical Equilibrium Chapter 18 Equilibrium, a Dynamic State • Many chemical reactions are reversible under ordinary conditions of temperature and concentration. • They will reach a state of equilibrium unless at least one of the substances involved escapes or is removed from the reaction system. • When the products of the forward reaction are favored, there is a higher concentration of products than of reactants at equilibrium. • The equilibrium “lies to the right”

  6. Section 1 The Nature of Chemical Equilibrium Chapter 18 Equilibrium, a Dynamic State, continued • When the products of the reverse reaction are favored, there is a higher concentration of reactants than of products at equilibrium. • the equilibrium “lies to the left” • In other cases, both forward and reverse reactions occur to nearly the same extent before chemical equilibrium is established. • Neither reaction is favored, and considerable concentrations of both reactants and products are present at equilibrium.

  7. Section 1 The Nature of Chemical Equilibrium Chapter 18 Equilibrium, a Dynamic State, continued • products of the forward reaction favored, lies to the right • products of the reverse reaction favored,lies to the left • Neither reaction is favored

  8. Section 1 The Nature of Chemical Equilibrium Chapter 18 • The Equilibrium Constant • The numerical value of K for a particular equilibrium system is obtained experimentally. • If K is equal to 1 at equilibrium, there are roughly equal concentrations of reactants and products.

  9. Section 1 The Nature of Chemical Equilibrium Chapter 18 The Equilibrium Expression, continued • The Equilibrium Constant, continued • If the value of K is small, the reactants are favored. • A large value of K indicates that the products are favored. • Only the concentrations of substances that can actually change are included in K. • Pure solids and liquids are omitted because their concentrations cannot change.

  10. Section 1 The Nature of Chemical Equilibrium Chapter 18 The Equilibrium Expression, continued The Equilibrium Constant, continued • The equilibrium constant, K, is the ratio of the mathematical product of the concentrations of substances formed at equilibrium to the mathematical product of the concentrations of reacting substances. Each concentration is raised to a power equal to the coefficient of that substance in the chemical equation. • The equation for K is sometimes referred to as thechemical equilibrium expression.

  11. Section 2 Shifting Equilibrium Chapter 18 Lesson Starter • Imagine children playing on a seesaw. • Five boys are sitting on one side and five girls on the other, and the seesaw is just balanced. • Then, one girl gets off, and the system is no longer at equilibrium. • One way to get the seesaw in balance again is for one of the boys to move toward the girls’ side.

  12. Section 2 Shifting Equilibrium Chapter 18 Lesson Starter, continued • When he gets to the middle, the seesaw is again at equilibrium. • The stress of one girl getting off is relieved by having one of the boys move his position. • How would a chemical system in equilibrium respond to removing one of the products?

  13. Section 2 Shifting Equilibrium Chapter 18 Predicting the Direction of Shift • Changes in pressure, concentration, or temperature can alter the equilibrium position and thereby change the relative amounts of reactants and products. • Le Châtelier’s principle states that if a system at equilibrium is subjected to a stress, the equilibrium is shifted in the direction that tends to relieve the stress. • This principle is true for all dynamic equilibria, chemical as well as physical. • Changes in pressure, concentration, and temperature illustrate Le Châtelier’s principle.

  14. Section 2 Shifting Equilibrium Chapter 18 Factors Affecting Equilibrium Click below to watch the Visual Concept. Visual Concept

  15. Temperature Changes Affect an Equilibrium System Section 2 Shifting Equilibrium Chapter 18

  16. Section 2 Shifting Equilibrium Chapter 18 Reactions That Go to Completion • Some reactions involving compounds formed by the chemical interaction of ions in solutions appear to go to completion in the sense that the ions are almost completely removed from solution. • The extent to which reacting ions are removed from solution depends on the solubility of the compound formed and, if the compound is soluble, on the degree of ionization.

  17. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Lesson Starter • pH of 0.10 M HCl _________________ • pH of 0.10 M CH3COOH ____________ • Why is the pH of the 0.10 M HCl different from the pH of the 0.10 M CH3COOH?

  18. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Lesson Starter, continued • pH of 0.10 M NaOH __________________ • pH 0.10 M NH3 _____________________ • Why is the pH of the 0.10 M NaOH different from the pH of the 0.10 M NH3?

  19. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Buffers • Buffered solutionsresist changes in pH. • Buffered solutions contains both a weak acid and a salt of the weak acid • example: CH3COOH and NaCH3COO– • Buffered solution can react with either an acid or a base. When small amounts of acids or bases are added, the pH of the solution remains nearly constant.

  20. Buffered Vs. Nonbuffered Solutions Section 3 Equilibria of Acids, Bases, and Salts Chapter 18

  21. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Buffers, continued • If a small amount of acid is added to the acetic acid– sodium acetate solution, acetate ions react with most of the added hydronium ions to form nonionized acetic acid molecules. • The hydronium ion concentration and the pH of the solution remain practically unchanged.

  22. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Buffers, continued • If a small amount of a base is added, the OH− ions of the base react with and remove hydronium ions to form nonionized water molecules. Acetic acid molecules then ionize and mostly replace the hydronium ions neutralized by the added OH− ions. • The hydronium ion concentration and the pH of the solution remain practically unchanged.

  23. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Buffers, continued • A solution of a weak base containing a salt of the base also behaves as a buffered solution. • Buffer action has many important applications in chemistry and physiology. • Human blood is naturally buffered to maintain a pH of between 7.3 and 7.5.

  24. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Hydrolysis of Salts • Salts are formed during the neutralization reaction between a Brønsted acid and a Brønsted base. • When a salt dissolves in water, it produces • positive ions (cations) of the base from which it was formed • negative ions (anions) of the acid from which it was formed • If the ions formed are from weak acids or bases, they react chemically with the water molecules, and the pH of the solution will have a value other than 7.

  25. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Hydrolysis of Salts, continued • A reaction between water molecules and ions of a dissolved salt ishydrolysis. • If the anions react with water, the process is anion hydrolysis and results in a more basic solution. • If the cations react with water molecules, the process is cation hydrolysis and results in a more acidic solution.

  26. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Hydrolysis of Salts, continued Anion Hydrolysis • In the Brønsted sense, the anion of the salt is the conjugate base of the acid from which it was formed. • It is also a proton acceptor. • If the acid is weak, its conjugate base (the anion) will be strong enough to remove protons from some of the water molecules. • An equilibrium is established in which the net effect of the anion hydrolysis is an increase in the hydroxide ion concentration, [OH−], of the solution.

  27. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Hydrolysis of Salts, continued Hydrolysis in Acid-Base Reactions • Hydrolysis can help explain why the end point of a neutralization reaction can occur at a pH other than 7. • Salts can be placed in four general categories, depending on their hydrolysis properties: • strong acid–strong base • strong acid–weak base • weak acid–strong base • weak acid–weak base

  28. Section 3 Equilibria of Acids, Bases, and Salts Chapter 18 Hydrolysis of Salts, continued Hydrolysis in Acid-Base Reactions, continued • Salts of strong acids and strong bases produce neutral solutions. • Neither the cation of a strong base nor the anion of a strong acid hydrolyzes appreciably in aqueous solutions. • The aqueous solutions of salts formed from reactions between weak acids and strong bases are basic. • Anions of the dissolved salt are hydrolyzed by the water molecules, and the hydroxide-ion concentration increases. This raises the pH of the solution.

  29. End of Chapter 18 Show

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