Acid-Base Equilibrium DrillProblems AP Chemistry Carol Brown Saint Mary’s Hall.

Slides:



Advertisements
Similar presentations
AQUEOUS EQUILIBRIA AP Chapter 17.
Advertisements

1 Chapter Fourteen Aqueous Equilibria. 2 The Common Ion Effect and Buffer Solutions Common ion effect - solutions in which the same ion is produced by.
Buffer This. There are two common kinds of buffer solutions: 1Solutions made from a weak acid plus a soluble ionic salt of the weak acid. 2Solutions made.
Buffers and Titrations
Created by C. Ippolito Jan 2007 Acid Base Reactions Objectives: 1.Calculate hydrogen ion and hydroxide ion concentrations 2.Calculate pH values 3.Explain.
Acid-Base Titrations. Acid-Base Equilibria Chapter 16.
ACID-BASE TITRATIONS Lesson 10. Acid-Base Titrations… PART I: what is a titration? how is it performed? what tools are needed? PART II: Perform Titration.
An Introduction to Volumetric Analysis
Acid-Base Equilibria and Solubility Equilibria Chapter
Chapter 17 Equilibrium in the Aqueous Phase. Clickers in Action © 2009 W. W. Norton & Company, Inc.2 What are the major species present in an aqueous.
Burette clamp ring stand burette erlenmeyer flask Titration.
Solutions are homogeneous mixtures consisting of two or more components. The major component of a solution is known as the solvent and the minor component.
Concentration of Solutions
VOLUMETRIC AND GRAVIMETRIC EXAM QUESTIONS
Chemistry 1011 TOPIC TEXT REFERENCE Acids and Bases
Buffers A buffer is a solution that is highly resistant to changes in pH when a strong acid or base is added. A buffer solution also has a pH close to.
Reactions in Aqueous Solutions II: Calculations Chapter 11.
CHM 112 Summer 2007 M. Prushan Acid-Base Equilibria and Solubility Equilibria Chapter 16.
Aqueous Equilibria Chapter 15 Applications of Aqueous Equilibria.
A.P. Chemistry Chapter 15 Applications of Aqueous Equuilibria.
Acid-Base Titration and pH
Chapter 18 – Other Aspects of Aqueous Equilibria Objectives: 1.Apply the common ion effect. 2.Describe the control of pH in aqueous solutions with buffers.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Additional Aqueous Equilibria CHAPTER 16
Acid-Base and Solubility Equilibria Common-ion effect Buffer solutions Acid-base titration Solubility equilibria Complex ion formation Qualitative analysis.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Dr. Ali Bumajdad.
Acid-Base Equilibria and Solubility Equilibria Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
1 TitrationsTitrations pHpH Titrant volume, mL At what point in a reaction does neutralization occur?
1 19 Ionic Equilibria: Part II Buffers and Titration Curves.
3 Acids, Bases, and Buffers
Prepared by PhD Halina Falfushynska 1 Lecture 7. Electrolytes. Reactions in Aqueous Solutions.
1 Chapter 17a Ionic Equilibria: Part II Buffers and Titration Curves.
AP/IB Chemistry Chapter 4: Aqueous Solutions and Solution Stoichiometry.
Aqueous Equilibria © 2009, Prentice-Hall, Inc. Chapter 17 Additional Aspects of Aqueous Equilibria Chemistry, The Central Science, 11th edition Theodore.
Chapter 17 Additional Aspects of Aqueous Equilibria Subhash Goel South GA State College Douglas, GA © 2012 Pearson Education, Inc.
Aqueous Equilibria Chapter 15 Additional Aspects of Aqueous Equilibria © 2009, Prentice-Hall, Inc.
Titrations Main Idea: Titrations are an application of acid-base neutralization reactions that require the use of an indicator.
CHM 108 SUROVIEC SPRING 2014 Chapter 4 Part 2. I. Solution Stoichiometry According to the following reaction, how many moles of Fe(OH)2 can form from.
Aqueous Equilibria Chapter 17 Additional Aspects of Aqueous Equilibria You love Chemistry You might have doubts, but deep, deep, deep down you know there.
Acid-Base Equilibria and Solubility Equilibria Chapter 17 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Additional Aspects of Aqueous Equilibria Chapter 17.
Chapter 19 Buffers and Titrations. The Common Ion Effect & Buffer Solutions 2 ______________- solutions in which the same ion is produced by two different.
Acids and Bases.
Bettelheim, Brown, Campbell and Farrell Chapter 9
19.1 Acid-Base Theories> 1 Copyright © Pearson Education, Inc., or its affiliates. All Rights Reserved. Day The pH for a 0.10 M solution of a.
Chapter 19: Acids, Bases, and Salts
Acid-Base Titration. Acid-base titration is a laboratory procedure used to determine – among other things – the unknown concentration of an acid or a.
Chapter 17 Sections 1-3 Common ions, Buffers and Titration © 2012 Pearson Education, Inc.
Volumetric Analysis – Titrations Volumetric Analysis a process of analysis accomplished by adding together particular volumes of 2 solutions the objective.
1 Titrations (Review) In a titration a solution of accurately known concentration is added gradually added to another solution of unknown concentration.
1 Chapter 15 Aqueous Equilibrium AP Chemistry Unit 12.
Ch 17: Additional Aspects of Aqueous Equilibria Brown, LeMay Ch 17 AP Chemistry.
Chapter 16: Aqueous Ionic Equilibria CHE 124: General Chemistry II Dr. Jerome Williams, Ph.D. Saint Leo University.
Titrations Chapter 13.
Chapter 17 Additional Aspects of Aqueous Equilibria.
Acid-Base Equilibria and Solubility Equilibria Chapter 17 Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
PROPERTIES OF SOLUTIONSPROPERTIES OF SOLUTIONSPROPERTIES OF SOLUTIONSPROPERTIES OF SOLUTIONS 1. A solution is composed of: solute the solute : the minor.
BUFFERS Mixture of an acid and its conjugate base. Buffer solution  resists change in pH when acids or bases are added or when dilution occurs. Mix: A.
Obj. finish 17.2, ) The pH range is the range of pH values over which a buffer system works effectively. 2.) It is best to choose an acid with.
Stoichiometry: Quantitative Information About Chemical Reactions Chapter 4.
© 2009, Prentice-Hall, Inc. Molarity Two solutions can contain the same compounds but be quite different because the proportions of those compounds are.
Effect of Structure on Acid-Base Properties. Applications of Aqueous Equilibria.
Solutions - Quantitatively. Solutions Mixture of at least two components Mixture of at least two components Solute Solute Solvent Solvent Components can.
Aqueous Equilibria Follow-up
Chemical Calculations
Acid Base Equilibrium.
Ionic Equilibria: Part II Buffers and Titration Curves
Dissociation Equilibria for weak acids and bases
What are acids and bases?. Monoprotic and diprotic acids Many acids are called monoprotic acids. This means that they only donate one mole of protons.
Presentation transcript:

Acid-Base Equilibrium DrillProblems AP Chemistry Carol Brown Saint Mary’s Hall

Problem 1 CH 3 NH 2 + H 2 O  CH 3 NH OH - Methylamine, CH 3 NH 2, is a weak base that reacts according to the equation above. The value of the ionization constant, K b, is 5.25  Methylamine forms salts such as methylammonium nitrate, (CH 3 NH 3 + )(NO 3 - ). (a) Calculate the hydroxide ion concentration, [OH - ], of a molar aqueous solution of methylamine. (b) Calculate the pH of a solution made by adding mole of solid methylammonium nitrate to milliliters of a molar solution of methylamine. Assume no volume change occu rs. (c) How many moles of either NaOH or HCl (state clearly which you choose) should be added to the solution in (b) to produce a solution that has a pH of 11.00? Assume that no volume change occurs. (d) A volume of 100. milliliters of distilled water is added to the solution in (c). How is the pH of the solution affected? Explain.

Methylamine, CH 3 NH 2, is a weak base that reacts according to the equation above. The value of the ionization constant, K b, is 5.25  Methylamine forms salts such as methylammonium nitrate, (CH 3 NH 3 + )(NO 3 - ). (a) Calculate the hydroxide ion concentration, [OH - ], of a molar aqueous solution of methylamine. Answer: 1.08 x M

(b)Calculate the pH of a solution made by adding mole of solid methylammonium nitrate to milliliters of a molar solution of methylamine. Assume no volume change occurs. Answer:

(c)How many moles of either NaOH or HCl (state clearly which you choose) should be added to the solution in (b) to produce a solution that has a pH of 11.00? Assume that no volume change occurs.

(d) A volume of 100. milliliters of distilled water is added to the solution in (c). How is the pH of the solution affected? Explain. The ratio does not change in this buffer solution with dilution, therefore, no effect on pH.

Problem 2 NH 3 + H 2 O  NH OH - Ammonia is a weak base that dissociates in water as shown above. At 25˚C, the base dissociation constant, K b, for NH 3 is 1.8  (a)Determine the hydroxide ion concentration and the percentage dissociation of a molar solution of ammonia at 25˚C. (b)Determine the pH of a solution prepared by adding mole of solid ammonium chloride to 100. millilitres of a molar solution of ammonia. (c)If mole of solid magnesium chloride, MgCl 2, is dissolved in the solution prepared in part (b) and the resulting solution is well-stirred, will a precipitate of Mg(OH) 2 form? Show calculations to support your answer. (Assume the volume of the solution is unchanged. The solubility product constant for Mg(OH) 2 is 1.5 

(a) Determine the hydroxide ion concentration and the percentage dissociation of a molar solution of ammonia at 25˚C x M

(b) Determine the pH of a solution prepared by adding mole of solid ammonium chloride to 100. milliliters of a molar solution of ammonia. Answer: 8.732

(c)If mole of solid magnesium chloride, MgCl 2, is dissolved in the solution prepared in part (b) and the resulting solution is well-stirred, will a precipitate of Mg(OH) 2 form? Show calculations to support your answer. (Assume the volume of the solution is unchanged. The solubility product constant for Mg(OH) 2 is 1.5  [OH - ] must be less than 4.3 x M. The [OH - ] of the buffer solution is 5.4 x M which is larger than allowed. Therefore a precipitate will form.

Problem 3 Sodium benzoate, C 6 H 5 COONa, is the salt of a the weak acid, benzoic acid, C 6 H 5 COOH. A 0.10 molar solution of sodium benzoate has a pH of 8.60 at room temperature. (a) Calculate the [OH - ] in the sodium benzoate solution described above. (b) Calculate the value for the equilibrium constant for the reaction: C 6 H 5 COO - + H 2 O   C 6 H 5 COOH + OH - (c) Calculate the value of K a, the acid dissociation constant for benzoic acid. (d)A saturated solution of benzoic acid is prepared by adding excess solid benzoic acid to pure water at room temperature. Since this saturated solution has a pH of 2.88, calculate the molar solubility of benzoic acid at room temperature.

(a) Calculate the [OH - ] in the sodium benzoate solution described above. Answer: 3.98 x M

(b) Calculate the value for the equilibrium constant for the reaction: C 6 H 5 COO - + H 2 O   C 6 H 5 COOH + OH x

(c) Calculate the value of K a, the acid dissociation constant for benzoic acid. 6.3 x 10 -5

(d) A saturated solution of benzoic acid is prepared by adding excess solid benzoic acid to pure water at room temperature. Since this saturated solution has a pH of 2.88, calculate the molar solubility of benzoic acid at room temperature. 2.8 x mol/L

Problem 4 A g sample of an impure monobasic amine is titrated to the equivalence point with 75.00mL 0f M HCl. The pH after mL of acid was added was The molecular weight of the base is known to be (a) What is its percent purity? (b) Calculate the ionization constant of this base (c) What is the pH at the equivalence point? (d) Which indicator from the following list would be most suitable for this titration? Orange IV (red-yellow; pH Methyl orange (red-yellow; pH ) Methyl Red (red-yellow; pH ) Bromthymol blue (yellow-blue; pH ) Phenolphthalein (colorless-pink; pH ) Thymolphthalein (colorless-blue; pH )

A g sample of an impure monobasic amine is titrated to the equivalence point with 75.00mL 0f M HCl. The pH after mL of acid was added was The molecular weight of the base is known to be (a) What is its percent purity? 88.65%

A g sample of an impure monobasic amine is titrated to the equivalence point with 75.00mL 0f M HCl. The pH after mL of acid was added was The molecular weight of the base is known to be (b) Calculate the ionization constant of this base. K b =5.1 x 10 -4

A g sample of an impure monobasic amine is titrated to the equivalence point with 75.00mL 0f M HCl. The pH after mL of acid was added was The molecular weight of the base is known to be (c) What is the pH at the equivalence point? C) pH = 5.85

A g sample of an impure monobasic amine is titrated to the equivalence point with 75.00mL 0f M HCl. The pH after mL of acid was added was The molecular weight of the base is known to be (d) Which indicator from the following list would be most suitable for this titration? Orange IV (red-yellow; pH Methyl orange (red-yellow; pH ) Methyl Red (red-yellow; pH ) Bromthymol blue (yellow-blue; pH ) Phenolphthalein (colorless-pink; pH ) Thymolphthalein (colorless-blue; pH ) Methyl Red

Problem 5 A buffer solution contains 0.40 mol of formic acid, HCOOH, and 0.60 mole of sodium formate, HCOONa, in 1.00 L of solution. The ionization constant, K a, of formic acid is 1.8 x A) Calculate the pH of this solution. B) If 100. milliliters of this buffer solution is diluted to a volume of 1.00 L with pure water, the pH does not change. Discuss why the pH remains constant on dilution. C) A 5.00 mL sample of 1.00 M HCl is added to 100. mL of the original buffer solution. Calculate the [H 3 O + ]of the resulting solution. D) A 800. mL sample of 2.00 molar formic acid is mixed with 200. mL 4.80 M NaOH. Calculate the [H 3 O + ] of the resulting solution.

A buffer solution contains 0.40 mol of formic acid, HCOOH, and 0.60 mole of sodium formate, HCOONa, in 1.00 L of solution. The ionization constant, K a, of formic acid is 1.8 x A) Calculate the pH of this solution. pH = 3.92

A buffer solution contains 0.40 mol of formic acid, HCOOH, and 0.60 mole of sodium formate, HCOONa, in 1.00 L of solution. The ionization constant, K a, of formic acid is 1.8 x B) If 100. milliliters of this buffer solution is diluted to a volume of 1.00 L with pure water, the pH does not change. Discuss why the pH remains constant on dilution. Ratio [A - ]/[HA] does not change.

A buffer solution contains 0.40 mol of formic acid, HCOOH, and 0.60 mole of sodium formate, HCOONa, in 1.00 L of solution. The ionization constant, K a, of formic acid is 1.8 x C) A 5.00 mL sample of 1.00 M HCl is added to 100. mL of the original buffer solution. Calculate the [H 3 O + ]of the resulting solution. [H 3 O + ] = 1.5 x 10 -4

A buffer solution contains 0.40 mol of formic acid, HCOOH, and 0.60 mole of sodium formate, HCOONa, in 1.00 L of solution. The ionization constant, K a, of formic acid is 1.8 x D) A 800. mL sample of 2.00 molar formic acid is mixed with 200. mL 4.80 M NaOH. Calculate the [H 3 O + ] of the resulting solution. [H 3 O + ]=1.2 x 10 -4

Problem 6 The molecular weight of a monoprotic acid, HX, was to be determined. A sample of grams of HX was dissolved in distilled water and the volume brought to exactly mL in a volumetric flask. Several mL portions of this solution were titrated against NaOH solution requiring an average of mL of NaOH. The NaOH solution was standardized against oxalic acid dihydrate, H 2 C 2 O 4. 2H 2 O (molar mass: g/mol). The volume of NaOH solution required to neutralize grams of oxalic acid dihydrate was mL. A) Calculate the molarity of the NaOH solution. B) Calculate the number of moles of HX in a mL portion used for titration. C) Calculate the molecular weight of HX. D) Discuss the effect of the calculated molecular weight of HX if the sample of oxalic acid dihydrate contained a non-acidic impurity.

The molecular weight of a monoprotic acid, HX, was to be determined. A sample of grams of HX was dissolved in distilled water and the volume brought to exactly mL in a volumetric flask. Several mL portions of this solution were titrated against NaOH solution requiring an average of mL of NaOH. The NaOH solution was standardized against oxalic acid dihydrate, H 2 C 2 O 4. 2H 2 O (molar mass: g/mol). The volume of NaOH solution required to neutralize grams of oxalic acid dihydrate was mL. A) Calculate the molarity of the NaOH solution M

The molecular weight of a monoprotic acid, HX, was to be determined. A sample of grams of HX was dissolved in distilled water and the volume brought to exactly mL in a volumetric flask. Several mL portions of this solution were titrated against NaOH solution requiring an average of mL of NaOH. The NaOH solution was standardized against oxalic acid dihydrate, H 2 C 2 O 4. 2H 2 O (molar mass: g/mol). The volume of NaOH solution required to neutralize grams of oxalic acid dihydrate was mL. B) Calculate the number of moles of HX in a mL portion used for titration mol HX in mL

The molecular weight of a monoprotic acid, HX, was to be determined. A sample of grams of HX was dissolved in distilled water and the volume brought to exactly mL in a volumetric flask. Several mL portions of this solution were titrated against NaOH solution requiring an average of mL of NaOH. The NaOH solution was standardized against oxalic acid dihydrate, H 2 C 2 O 4. 2H 2 O (molar mass: g/mol). The volume of NaOH solution required to neutralize grams of oxalic acid dihydrate was mL. C) Calculate the molecular weight of HX g/mol

The molecular weight of a monoprotic acid, HX, was to be determined. A sample of grams of HX was dissolved in distilled water and the volume brought to exactly mL in a volumetric flask. Several mL portions of this solution were titrated against NaOH solution requiring an average of mL of NaOH. The NaOH solution was standardized against oxalic acid dihydrate, H 2 C 2 O 4. 2H 2 O (molar mass: g/mol). The volume of NaOH solution required to neutralize grams of oxalic acid dihydrate was 41.24,:/ D) Discuss the effect of the calculated molecular weight of HX if the sample of oxalic acid dihydrate contained a non-acidic impurity. –The calculated molecular weight is smaller than true value, because: –measured g H 2 C 2 O 4 is larger than true value, –calculated mol H 2 C 2 O 4 is larger than true value, –calculated mol NaOH is larger than true value, –calculated M NaOH is larger than true value –calculated mol HX is larger than true value, therefore, Molar mass is smaller.