3.6: ACIDS AND BASES … Workbook pgs 145- 148… Buffered Solutions…

Slides:



Advertisements
Similar presentations
Chapter 17 Additional Acid/ Base Equilibria Buffers Common Ion Effects
Advertisements

Buffer Capacity Lab.
BUFFER SOLUTIONS LAB 9. INTRODUCTION Adding trace amount of acid to water will result in increase in H + concentration. In the same manner, adding trace.
Applications of Aqueous Equilibria
Chapter 16: Aqueous Ionic Equilibria Common Ion Effect Buffer Solutions Titrations Solubility Precipitation Complex Ion Equilibria.
Entry Task: Feb 12th Tuesday
Buffers. Buffered Solutions. A buffered solution is one that resists a change in its pH when either hydroxide ions or protons (H 3 O + ) are added. Very.
Chapter 17 Additional Aspects of Aqueous Equilibria
Updates Assignment 05 is is due today (in class) Midterm 2 is Thurs., March 15 –Huggins 10, 7-8pm –For conflicts: ELL 221, 6-7pm (must arrange at least.
Chapter 17: Additional Aspects of Acid-Base Equilibria
Aqueous Equilibria © 2009, Prentice-Hall, Inc. The Common-Ion Effect Consider a solution of acetic acid: If acetate ion is added to the solution, Le Châtelier.
Chapter 15 Applications of Aqueous Equilibria. The Common-Ion Effect Common-Ion Effect: The shift in the position of an equilibrium on addition of a substance.
EQUILIBRIUM Part 1 Common Ion Effect. COMMON ION EFFECT Whenever a weak electrolyte and a strong electrolyte share the same solution, the strong electrolyte.
Chemistry 1011 TOPIC TEXT REFERENCE Acids and Bases
Buffers AP Chemistry.
Aqueous Equilibria Bicarbonate buffer system. Aqueous Equilibria Buffers: What are they????? Solutions of a weak acid and its conjugate Or a weak base/conjugate.
Section 2: Buffered Solutions.  Solutions prepared with common ions have a tendency to resist drastic pH changes even when subjected to the addition.
Aqueous Equilibria Chapter 15 Applications of Aqueous Equilibria.
Prepared by Prof. Odyssa Natividad R.M. Molo. Consider a solution that contains not only a weak acid (HC 2 H 3 O 2 ) but also a soluble salt (NaC 2 H.
Chapter 15 Buffers Titration pH Curves
Monoprotic Acid- Base Equilibria K w = [ H + ] [ HO - ] = 1.0 x log K w = pH + pOH = at 25 o C So what is the pH of 1.0 x M KOH? [H.
Part 2 Chapter 17. Salt Solutions We will look at the cation and the anion separately, and then combine the result to determine whether the solution is.
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 (Buffers ) Green & Damji Chapter 8, Section 18.2 Chang Chapter 16 Copyright © The McGraw-Hill Companies, Inc. Permission required.
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.
Chapter 14 Equilibria in Acid-Base Solutions. Buffers: Solutions of a weak conjugate acid-base pair. They are particularly resistant to pH changes, even.
Aqueous Equilibria Chapter 15 Additional Aspects of Aqueous Equilibria © 2009, Prentice-Hall, Inc.
AP Chapter 17 Additional Aspects of Equilibrium Acid Base and Solubility Equilibria HW:7, 15, 29, 39,
ANALYTICAL CHEMISTRY CHEM 3811 CHAPTER 9 DR. AUGUSTINE OFORI AGYEMAN Assistant professor of chemistry Department of natural sciences Clayton state university.
Ch. 17 – Other Aspects of Equilibrium The concept of equilibrium may be used to describe the solubility of salts and the buffering action of a solution.
Aqueous Equilibria Chapter 17 Additional Aspects of Aqueous Equilibria.
Acids and Bases © 2009, Prentice-Hall, Inc. Chapters 15 &16 Acids and Bases.
Weak acids and buffers Numerical estimates.. Weak acids Weak acids are characterized by less than 100% dissociation. A “weak” acid is not necessarily.
Copyright©2000 by Houghton Mifflin Company. All rights reserved. 1 Chemistry FIFTH EDITION by Steven S. Zumdahl University of Illinois Chapter 15 Applications.
Entry Task: Jan 22 nd Thursday Turn in Determine Ka Lab.
Aqueous Equilibria Chapter 15 Applications of Aqueous Equilibria.
The doctrine about solution. Buffer solution KARAGANDA STATE MEDICAL UNIVERSITY Karaganda 2014y.
C H E M I S T R Y Chapter 15 Applications of Aqueous Equilibria.
8.3 Bases Similar to weak acids, weak bases react with water to a solution of ions at equilibrium. The general equation is: B(aq) + H2O(l)  HB+(aq) +
Chapter 17 Sections 1-3 Common ions, Buffers and Titration © 2012 Pearson Education, Inc.
1081. y = 1.0 x M [OH - ] = 1.0 x M 1082.
Acid-Base Equilibria. Some Definitions Arrhenius – An acid is a substance that, when dissolved in water, increases the concentration of hydrogen ions.
Aspects of Aqueous Equilibria. Aspects of Aqueous Equilibria: The Common Ion Effect Recall that salts like sodium acetate are strong electrolytes NaC.
Chapter 17 Additional Aspects of Aqueous Equilibria John D. Bookstaver St. Charles Community College Cottleville, MO Lecture Presentation © 2012 Pearson.
Strength of Acids Strength of an acid is measured by the extent it reacts with water to form hydronium ions (H 3 O + ). Strong acids ionize ~100% so pH.
Ch 8: Introducing Acids and Bases. pH of precipitation in the United States 2001, and in Europe as reported in 2002.
Chapter 15 Applications of Aqueous Equilibria
Chapter 17 Additional Aspects of Aqueous Equilibria
Aqueous Equilibria The Common-Ion Effect Consider a solution of acetic acid: NaC 2 H 3 O 2 Le Châtelier says the equilibrium will shift to the ______.
Applications of Aqueous Equilibria
The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with one of the products.
Common Ion Effect, Buffers, and Titration March 4/6, 2015.
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.
ACID-BASE EQUILIBRIA AP CHEM CH 15. The Common Ion Effect The shift in equilibrium that occurs because of the addition of an ion already involved in the.
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.
Buffers and Titrations
Aim # 12: What is a Buffer Solution?
Other Aspects of Aqueous Equilbria:
Buffers Buffers are solutions of a weak conjugate acid-base pair.
Additional Aspects of Aqueous Equilibria
Obj 17.1, 17.2 Notes 17-1.
Chapter 17 Additional Aspects of Aqueous Equilibria
Chapter 17 Additional Aspects of Aqueous Equilibria
Chapter 17 Additional Aspects of Aqueous Equilibria
Presentation transcript:

3.6: ACIDS AND BASES … Workbook pgs … Buffered Solutions…

BUFFER SOLUTIONS Buffer Causes solutions to be resistant to a change in pH when a strong acid or base is added Mixture of a weak acid and salts of conjugate bases If you add mol of NaOH to 1.0 L of pure water the pH drops from 7 to 2 If you add mol of NaOH to 1.0 L of blood (pH of 7.4) the pH will drop to 7.3 Two requirements for a buffer: An acid capable of reacting with added OH - ions and a base that can consume added H 3 O + ions. The acid and base must not react with each other (acetic acid and acetate ion or ammonia and ammunium ions)

BUFFERS If a small amount of hydroxide is added to an equimolar solution of HF in NaF, for example, the HF reacts with the OH − to make F − and water.

BUFFERS: Similarly, if acid is added, the F − reacts with it to form HF and water.

MATH TIME: What is the pH of a 0.700M solution of acetic acid ? K a = 1.8 x pH = 2.45 What is the pH of a 0.600M solution of sodium acetate? K b = 5.6 x pH = 9.26 What is the pH of an acetic acid/sodium acetate buffer with [CH 3 CO 2 H] = 0.700M and [CH 3 CO 2 - ] = 0.600M? K a = 1.8 x pH = 4.68

BUFFER CALCULATIONS: Consider the equilibrium constant expression for the dissociation of a generic acid, HA: HA + H 2 OH 3 O + + A − [H 3 O + ] [A − ] [HA] K a =

© 2009, Prentice-Hall, Inc. BUFFER CALCULATIONS Rearranging slightly, this becomes [A − ] [HA] K a = [H 3 O + ] Taking the negative log of both side, we get [A − ] [HA] −log K a = −log [H 3 O + ] + − log pKapKa pH acid base

© 2009, Prentice-Hall, Inc. BUFFER CALCULATIONS So pK a = pH − log [base] [acid] Rearranging, this becomes pH = pK a + log [base] [acid] This is the Henderson–Hasselbalch equation.

HENDERSON-HASSELBALCH EQUATION: For when the concentrations of the acid and conjugate base are quite large… … or when you want a short cut to a buffer solution

PRACTICE: What is the pH of a buffer that is 0.12 M in lactic acid, CH 3 CH(OH)COOH, and 0.10 M in sodium lactate? K a for lactic acid is 1.4  10 −4. pH = pK a + log [base] [acid] pH = −log (1.4  10 −4 ) + log (0.10) (0.12) pH = (−0.08) = 3.77

PRACTICE: Benzoic acid (C 6 H 5 CO 2 H, 2.00g) and sodium benzoate (NaC 6 H 5 CO 2, 2.00g) are dissolved in enough water to make 1.00L of solution. Calculate the pH of the solution using the Henderson-Hasselbalch equation. K a = 6.3 x g benzoic acid = mol 2.00g sodium benzoate = mol pH = log( / ) = 4.13

PREPARING BUFFER SOLUTIONS Buffers work on a pH range: The pH range is the range of pH values over which a buffer system works effectively. It is best to choose an acid with a p K a close to the desired pH

PREPARING BUFFER SOLUTIONS: To be useful, a buffer solution must have 2 characteristics: pH control : pH = pK a + log [conjugatebbase] / [acid] Acid is chosen whose pK a is near the intended value of the pH Exact value of pH is then achieved by adjusting the acid-to- conjugate base ratio Buffer Capacity: Buffer should have the ability to keep the pH approximately constant after the addition of reasonable amounts of acid and base.

PREPARING BUFFER SOLUTIONS: You wish to prepare 1.0L of a buffer solution with a pH of A list of possible acids (and their conjugate bases) follows: Which combination should be selected, and what should the ratio of acid to conjugate base be? AcidConjugate Base KaKa pK a HSO 4 - SO x CH 3 CO 2 HCH 3 CO x HCO 3 CO x

PREPARING BUFFER SOLUTIONS: pH = 4.30, so [H 3 O + ] = 5.0 x Acetic acid (K a is the closest value of desire [H 3 O + ]) = 2.8 [CH 3 CO 2 − ] [CH 3 CO 2 H] K a = [H 3 O + ] [CH 3 CO 2 − ] [CH 3 CO 2 H] K a = [H 3 O + ] [CH 3 CO 2 − ] [CH 3 CO 2 H] 5.0 x = 1.8 x 10 -5

PREPARING BUFFER SOLUTIONS: Ratio of conjugate base to acid = 0.36 pH = pK a + log [base] [acid]

PREPARING BUFFER SOLUTIONS: The relative number of moles of acid and conjugate base is important in determining the pH of a buffer solution, not the concentration. Why? Volume cancels out! That means that diluting a buffer solution will not change its pH