16-1 CHEM 102, Fall 2010, LA TECH Instructor: Dr. Upali Siriwardane Office: CTH 311 Phone 257-4941 Office Hours: M,W 8:00-9:00.

Slides:



Advertisements
Similar presentations
Chapter 14 Arrhenius –Acid – create H + in water –Base – create OH - in water Bronsted-Lowery –Acid – donates proton (H + ) –Base – accepts proton (H +
Advertisements

Chapter 14 Acids and Bases 2006, Prentice hall.
CH. 16 ACID -- BASE 16.4 pH scale (pOH) 16.1 Definition 16.2
Acid-Base Equilibria BLB 12 th Chapter 16. Expectations  Distinguish between acids and bases Definitions & properties Know common strong and weak examples.
AP Chemistry – Chapter 16 Acid and Base Equilibrium HW:
Acid - Base Equilibria AP Chapter 16. Acids and Bases Arrhenius acids have properties that are due to the presence of the hydronium ion (H + ( aq )) They.
Quiz number 5 will be given in recitation next week, Feb 26-Mar 2
Prentice Hall © 2003Chapter 16 Chapter 16 Acid-Base Equilibria CHEMISTRY The Central Science 9th Edition David P. White.
Chapter 16 Acid-Base Equilibria. The H + ion is a proton with no electrons. In water, the H + (aq) binds to water to form the H 3 O + (aq) ion, the hydronium.
1 Acids and Bases Chapter Why are lemons sour?
Copyright 1999, PRENTICE HALLChapter 161 Acid-Base Equilibria Chapter 16 David P. White University of North Carolina, Wilmington.
AP CHEMISTRY.  Acids ◦ Sour, can corrode metals, cause certain dyes to change colors  Bases ◦ Bitter taste, feel slippery, usually used in cleaning.
Introduction to Acids and Bases AP Chemistry
A.P. Chemistry Chapter 14 Acid- Base Chemistry Arrhenius Acid- an acid is any substance that dissolves in water to produce H + (H 3 O + ) ions Base-
Acids and Bases Topics to be covered: Definitions of acids and bases; Bronsted’s conjugate acid-base pairs concept; Determination of [H 3 O + ], [OH -
Chapter 14 Acids and Bases
Acids and Bases Chemistry 2013.
N Acid/Base Definitions n Types of Acids/bases n Polyprotic Acids n The Ion Product for Water n The pH and Other “p” Scales n Aqueous Solutions of Acids.
Chapter 16 Acid–Base Equilibria
Chapter 16 Acids and Bases. © 2009, Prentice-Hall, Inc. Some Definitions Arrhenius – An acid is a substance that, when dissolved in water, increases the.
Chapter 10 Acids and Bases.
Chapter [ ] Acids and Bases Equilibria. Arrhenius (or Classical) Acid-Base Definition An acid is a substance that contains hydrogen and dissociates.
Chapter 14 Acids and Bases. Acid/Base Theories Arrhenius Theory –Acids produce H + ions in solution –Bases produce OH - ions in solution –Downside Must.
I. Introduction to Acids & Bases
CTH :00-11:15 am Instructor: Dr. Upali Siriwardane Office: 311 Carson Taylor Hall ; Phone: ; Office Hours:
Unit 6 - Chpt 14&15 - Acid/Base Acid basics, strengths, etc. pH scale, calculations Base basics Polyprotic acids, Acid/Base properties of salts, hydrolysis,
Acids and Bases  Arrhenius ◦ Acid:Substance that, when dissolved in water, increases the concentration of hydrogen ions. ◦ Base:Substance that, when dissolved.
Chemistry 102(01) spring 2009 Instructor: Dr. Upali Siriwardane
Prentice Hall ©2004 Chapter 14 Aqueous Equilibria: Acids and Bases.
Chapter 16 Acid–Base Equilibria
ACID-BASE TITRATIONS PART 3. WHAT DOES THE TITRATION GRAPH TELL? If we have a solid that dissolves: A 2 B (s)  2 A (aq) + B (aq) Then K sp is calculated.
14.1 Intro to Acids and Bases 14.2 Acid Strength 14.3 pH Scale
Acids, Bases, and Salts Chapter Acids – Taste sour – React with metals to form H 2 gas – Will change the color of and acid-base indicator Turns.
What are acids and bases?
Acid-Base Equilibria. Acids Bases Sour taste React with active metals to release hydrogen gas Change the color of indicators Bitter taste Feel slippery.
Chapter 14 Acids and Bases. Lemons contain citric acid, Citric acid produces H + ions in your mouth H + ions react with protein molecules on your tongue.
Chemistry 102(060) Summer 2015 Instructor: Dr. Upali Siriwardane
ACIDS & BASES Arrhenius Theory 1. in aqueous solution 2. Acid: produces H + 3. Base: produces OH -
Chapter 15 &. Properties of acids n Taste Sour (kids, don’t try this at home). n Conduct electricity. n Some are strong, some are weak electrolytes. n.
Acid Base Equilibrium CH 16. Some Definitions Arrhenius Acid:Substance that, when dissolved in water, increases the concentration of hydrogen ions. Base:Substance.
Acid/Base Definitions  Arrhenius Model  Acids produce hydrogen ions in aqueous solutions  Bases produce hydroxide ions in aqueous solutions  Bronsted-Lowry.
Chemistry 102(60) Summer 2002 Instructor: Dr. Upali Siriwardane Office: CTH 311 Phone Office Hours: 8:30-10;30 M, W,
Arrhenius Definition Acids produce hydrogen ions in aqueous solution. Acids produce hydrogen ions in aqueous solution.  H 2 SO 4, HCl, HC 2 H 3 O 2 Bases.
ACIDS AND BASES ACID – A compound that produces hydrogen ions in a water solution HCl (g) → H + (aq) + Cl - (aq) BASE – A compound that produces hydroxide.
ACIDS & BASES. ACID/BASE THEORY Acids and bases are solutions which can be described differently by multiple theories. So far, we have treated everything.
16-1 CHEM 102, Fall 2012, LA TECH CTH :00-11:15 am Instructor: Dr. Upali Siriwardane Office: CTH 311 Phone Office.
Acid-Base Equilibria BLB 10 th Chapter 16. Examples of acids & bases.
Chapter 16 : Acid-Base Equilibria Created by Lauren Querido.
Ch 16: Acid-Base Equilibria Brown, LeMay Ch 16 AP Chemistry.
Equilibrium – Acids and Bases. Review of Acids and Bases Arrhenius Theory of Acids and Bases ▫An acid is a substance that dissociates in water to produce.
ADVANCED PLACEMENT CHEMISTRY ACIDS, BASES, AND AQUEOUS EQUILIBRIA.
Acid & Base Solutions. Properties of Acids  What we know about acids:  Sour taste  pH 0 – 7  Turns blue litmus to red  Turns methyl orange to red.
Acids and Bases All you ever wanted to know, and more!
Taste sour Taste sour Form solution that conduct electricity Form solution that conduct electricity React with metals React with metals Turn blue litmus.
Acid-base Equilibria n K a and K b n % dissociation of weak acid/bases n pH of weak acid/base solutions n pH of salt solutions n Buffers n pH of buffer.
8–1 John A. Schreifels Chemistry 212 Chapter 16-1 Chapter 16 Acids and Bases.
Acids and Bases Arrhenius Definition Acids produce hydrogen ions in aqueous solution. Bases produce hydroxide ions when dissolved in water. Limits to.
Unit 11: Acid-Base Equilibrium Chapter 16 and 17 Problem Set Chapter 16: 17, 21, 37, 43, 45, 61, 65, 69, 77, 79, 101, 107 Chapter 17: 19, 23, 27, 31, 41,
AP CHEMISTRY.  Acids ◦ Sour, can corrode metals, cause certain dyes to change colors  Bases ◦ Bitter taste, feel slippery, usually used in cleaning.
I. Introduction to Acids & Bases Ch. 19 – Acids & Bases.
  Acids  Produce H + ions when dissolved in water  Ionize into H + ions and negative ion  (Ex. HCl, HBr)  Bases  Produce OH - ions when dissolved.
Chemistry 100 Acids and Bases. The Brønsted Definitions Brønsted Acid  proton donor Brønsted Base  proton acceptor Conjugate acid - base pair  an acid.
CHAPTER 16: ACID BASE EQUILIBRIA Wasilla High School
ACIDS AND BASES ACID – A compound that produces hydrogen ions in a water solution HCl (g) → H + (aq) + Cl - (aq) BASE – A compound that produces hydroxide.
1 Chapter 10 Acids & Bases. 2 CHAPTER OUTLINE  General Properties General Properties  Arrhenius Acids & Bases Arrhenius Acids & Bases  Brønsted-Lowery.
Chapter 17 Acids and Bases.
Acids and Bases: A Brief Review
Acid & BAses.
Acid Base Equilibria.
Presentation transcript:

16-1 CHEM 102, Fall 2010, LA TECH Instructor: Dr. Upali Siriwardane Office: CTH 311 Phone Office Hours: M,W 8:00-9:00 & 11:00-12:00 am; Tu,Th,F 8: :00 am. Test Dates : September 23, October 21, and November 16; Comprehensive Final Exam: November 18, 2010 Exam: 10:0-10:15 am, CTH 328. September 23, 2010 (Test 1): Chapter 13 October 21, 2010 (Test 2): Chapters 14 & 15 November 16, 2010 (Test 3): Chapters 16, 17 & 18 Comprehensive Final Exam: November 18, 2010 : Chapters 13, 14, 15, 16, 17 and 18 Chemistry 102(01) Fall 2010

16-2 CHEM 102, Fall 2010, LA TECH Chapter 16. Acids and Bases 16.1 The Brønsted-Lowry Concept of Acids and Bases 16.2 Types of acids/bases:Organic Acids and Amines 16.3 The Autoionization of Water 16.4 The pH Scale 16.5 Ionization Constants of Acids and Bases 16.6 Problem Solving Using K a and K b 16.7 Molecular Structure and Acid Strength 16.8 Acid-Base Reactions of Salts 16.9 Practical Acid-Base Chemistry Lewis Acid and Bases

16-3 CHEM 102, Fall 2010, LA TECH Types of Reactions a) Precipitation Reactions. Reactions of ionic compounds or salts Reactions of ionic compounds or salts b) Acid/base Reactions. Reactions of acids and bases Reactions of acids and bases c) Redox Reactions. reactions of oxidizing & reducing agents reactions of oxidizing & reducing agents

16-4 CHEM 102, Fall 2010, LA TECH What are Acids &Bases? Definition? a) Arrhenius b) Bronsted-Lowry c) Lewis

16-5 CHEM 102, Fall 2010, LA TECH Arrhenius, Svante August ( ), Swedish chemist, 1903 Nobel Prize in chemistry AcidAcid Anything that produces hydrogen ions in a water solution. HCl (aq ) H + ( aq) + Cl - ( aq) Base BaseAnything that producs hydroxide ions in a water solution. NaOH (aq) Na + ( aq) + OH - ( aq) Arrhenius definitions are limited proton acids and hydroxide bases to aqueous solutions. Arrhenius Definitions

16-6 CHEM 102, Fall 2010, LA TECH Expands the Arrhenius definitions to include many bases other than hydroxides and gas phase reactions Acid AcidProton donor Base BaseProton acceptor This definition explains how substances like ammonia can act as bases. Eg. HCl(g) + NH 3 (g) > NH 4 Cl(s) HCl (acid), NH 3 (base). NH 3 (g) + H 2 O(l) NH OH - Brønsted-Lowry definitions

16-7 CHEM 102, Fall 2010, LA TECH Lewis Definition G.N. Lewis was successful in including acid and bases without proton or hydroxyl ions. Lewis Acid: A substance that accepts an electron pair. Lewis base: A substance that donates an electron pair. E.g. BF 3 (g) + :NH 3 (g) F 3 B:NH 3 (s) the base donates a pair of electrons to the acid forming a coordinate covalent bond common to coordination compounds. Lewis acids/bases will be discussed later in detail

16-8 CHEM 102, Fall 2010, LA TECH Dissociation Strong Acids: HCl(aq) + H 2 O(l) H 3 + O(aq) + Cl - (aq) HCl(aq) + H 2 O(l) H 3 + O(aq) + Cl - (aq) H 2 SO 4 (aq) + H 2 O(l) H 3 + O(aq) + HSO 4 - (aq) H 2 SO 4 (aq) + H 2 O(l) H 3 + O(aq) + HSO 4 - (aq) Dissociation Equilibrium Weak Acid/base: Dissociation Equilibrium Weak Acid/base: H 2 O(l) + H 2 O(l) H 3 + O(aq) + OH - (aq) This dissociation is called autoionization of water. HC 2 H 3 O 2 (aq) + H 2 O(l) H 3 + O(aq) + C 2 H 3 O 2 - (aq) NH 3 (aq) + H 2 O(l) NH OH - (aq) Equilibrium constants: K a, K b and K w

16-9 CHEM 102, Fall 2010, LA TECH Conjugate acid-base pairs. Acids and bases that are related by loss or gain of H+ as H 3 O + and H 2 O. Examples. Examples.AcidBase H 3 O + H 2 O HC 2 H 3 O 2 C 2 H 3 O 2 - NH 4 + NH 3 H 2 SO 4 HSO 4 - HSO 4 - SO 4 2- Brønsted-Lowry Definitions

16-10 CHEM 102, Fall 2010, LA TECH Bronsted acid/conjugate base and base/conjugate acid pairs in acid/base equilibria HCl(aq) + H 2 O(l) H 3 + O(aq) + Cl - (aq) HCl(aq): acid H 2 O(l):base H 3 + O(aq):conjugate acid Cl - (aq):conjugate base H 2 O/ H 3 + O: base/conjugate acid pair HCl/Cl - :acid/conjugate base pair

16-11 CHEM 102, Fall 2010, LA TECH Select acid, base, acid/conjugate base pair, base/conjugate acid pair H 2 SO 4 (aq) + H 2 O(l) H 3 + O(aq) + HSO 4 - (aq) acid base conjugate acid conjugate base base/conjugate acid pair acid/conjugate base pair

16-12 CHEM 102, Fall 2010, LA TECH Types of Acids and Bases Binary acids: HCl, HBr, HI, H 2 S More than two elements: HCN Oxyacid: HNO 3, H 2 SO 4, H 3 PO 4 Polyprotic acids: H 2 SO 4, H 3 PO 4 Organic acids: R-COOH, R= CH 3 -, CH 3 CH 2 - Acidic oxides: SO 3, NO 2, CO 2, Basic oxides: Na 2 O, CaO Amine: NH 3. R-NH 2, R= CH 3 -, CH 3 CH 2 - : primary R 2 -NH : secondary, R 3 -N: tertiary R 2 -NH : secondary, R 3 -N: tertiary Lewis acids & bases: BF 3 and NH 3

16-13 CHEM 102, Fall 2010, LA TECH Strong Acid vs. Weak Acids Strong acid completely ionized Hydrioidic HI K a ~ pK a = -11 Hydrobromic HBr K a ~ 10 9 pK a = -9 Perchloric HClO 4 K a ~ 10 7 pK a = -7 Hyrdrochloric HCl K a ~ 10 7 pK a = -7 Chloric HClO 3 K a ~ 10 3 pK a = -3 Sulfuric H 2 SO 4 K a ~ 10 2 pK a = -2 Nitric HNO 3 K a ~ 20 pK a = -1.3 Weak acid partially ionized Hydrofluoric acid HF K a = 6.6x10 -4 pK a = 3.18 Formic acid HCOOH K a = 1.77x10 -4 pK a = 3.75 Acetic acid CH 3 COOH K a = 1.76x10 -5 pK a = 4.75 Nitrous acid HNO 2 K a = 4.6x10 -4 pK a = 3.34 Acetyl Salicylic acid C 9 H 8 O 4 K a = 3x10 -4 pK a = 3.52 Hydrocyanic acid HCN K a = 6.17x pK a = 9.21

16-14 CHEM 102, Fall 2010, LA TECH Strong Base vs. Weak Base Strong Base completely ionized Lithium hydroxide LiOH Sodium hydroxide NaOH Potassium hydroxide KOH K b ~ Rubidium hydroxide RbOH Cesium hydroxide CsOH Boarder-line Bases Magnesium hydroxide Mg(OH) 2 Calcium hydroxide Ca(OH) 2 Strotium hydroxide Sr(OH) 2 K b ~ 0.01 to0.1 Barium hydroxide Ba(OH) 2 Weak Base partially ionized Ammonia NH 3 K b =1.79x10 -5 pK b = 4.74 Ethyl amine CH 3 CH 2 NH 2 K b =5.6x10 -4 pK b = 3.25

16-15 CHEM 102, Fall 2010, LA TECH Strong acidsStrong acids Ionize completely in water. HCl, HBr, HI, HClO3, HNO3, HClO4, H2SO4. Weak acidsWeak acids Partially ionize in water. Most acids are weak. Strong basesStrong bases Ionize completely in water. Strong bases are metal hydroxides - NaOH, KOH Weak basesWeak bases Partially ionize in water. Acid and Base Strength

16-16 CHEM 102, Fall 2010, LA TECH Common Acids and Bases Acids Formula Molarity* nitricHNO 3 16 hydrochloric HCl 12 sulfuricH 2 SO 4 18 aceticHC 2 H 3 O 2 18 Bases ammoniaNH 3 (aq) 15 sodium hydroxideNaOH solid *undiluted.

16-17 CHEM 102, Fall 2010, LA TECH Autoionization Autoionization When water molecules react with one another to form ions. Acids and bases alter the dissociation equilibrium of water based on Le Chaterlier’s principle Kw = [ H3O + ] [ OH - ] = 1.0 x at 25 o C Note: Note: [H2O] is constant and is included in Kw. ion product of water ion product of water H2O(l) + H2O(l) H3O + (aq) + OH - (aq) (10 -7 M) (10 -7 M) Autoionization of Water

16-18 CHEM 102, Fall 2010, LA TECH We need to measure and use acids and bases over a very large concentration range. pH and pOH are systems to keep track of these very large ranges. pH = -log[H 3 O + ] pOH = -log[OH - ] pH + pOH = 14 Substance pH 1 M HCl0.0 Gastric juices Lemon juice Classic Coke2.5 Coffee5.0 Pure Water7.0 Blood Milk of Magnesia 10.5 Household ammonia M NaOH 14.0 Substance pH 1 M HCl0.0 Gastric juices Lemon juice Classic Coke2.5 Coffee5.0 Pure Water7.0 Blood Milk of Magnesia 10.5 Household ammonia M NaOH 14.0 pH and other “p” scales

16-19 CHEM 102, Fall 2010, LA TECH A logarithmic scale used to keep track of the large changes in [H + ] M M M Very Neutral Very acidic Basic When you add an acid to, the pH gets smaller. When you add a base to, the pH gets larger. pH scale

16-20 CHEM 102, Fall 2010, LA TECH Substance pH 1 M HCl0.0 Gastric juices Lemon juice Classic Coke2.5 Coffee5.0 Pure Water7.0 Blood Milk of Magnesia 10.5 Household ammonia M NaOH 14.0 Substance pH 1 M HCl0.0 Gastric juices Lemon juice Classic Coke2.5 Coffee5.0 Pure Water7.0 Blood Milk of Magnesia 10.5 Household ammonia M NaOH 14.0 pH of some common materials

16-21 CHEM 102, Fall 2010, LA TECH pH of Aqueous Solutions

16-22 CHEM 102, Fall 2010, LA TECH What is pH? K w = [H 3 + O][OH - ] = 1 x [H 3 + O][OH - ] = x Extreme cases: Extreme cases: Basic medium [H 3 + O][OH - ] = x 10 0 [H 3 + O][OH - ] = x 10 0 Acidic medium [H 3 + O][OH - ] = 10 0 x [H 3 + O][OH - ] = 10 0 x pH value is -log[H + ] spans only 0-14 in water.

16-23 CHEM 102, Fall 2010, LA TECH pH, pK w and pOH The relation of pH, K w and pOH K w = [H + ][OH - ] K w = [H + ][OH - ] log K w = log [H + ] + log [OH - ] log K w = log [H + ] + log [OH - ] -log K w = -log [H + ] -log [OH - ] ; -log K w = -log [H + ] -log [OH - ] ; previous equation multiplied by -1 pK w = pH + pOH; pK w = 14 pK w = pH + pOH; pK w = 14 since K w =1 x since K w =1 x = pH + pOH pH = 14 - pOH pOH = 14 - pH 14 = pH + pOH pH = 14 - pOH pOH = 14 - pH

16-24 CHEM 102, Fall 2010, LA TECH pH and pOH calculations of acid and base solutions a) Strong acids/bases dissociation is complete for strong acid such as HNO 3 or base NaOH [H + ] is calculated from molarity (M) of the solution b) weak acids/bases needs K a, K b or percent(%)dissociation

16-25 CHEM 102, Fall 2010, LA TECH pH of Strong Acid/bases HNO 3 (aq) + H 2 O(l) H 3 +O(aq) + NO 3 - (aq) HNO 3 (aq) + H 2 O(l) H 3 +O(aq) + NO 3 - (aq) Therefore, the moles of H + ions in the solution is equal to moles of HNO 3 at the beginning. [HNO 3 ] = [H + ] = 0.2 mole/L [HNO 3 ] = [H + ] = 0.2 mole/L pH = -log [H+] pH = -log [H+] = -log(0.2) = -log(0.2) pH = pH = Substance pH 1 M HCl0.0 Gastric juices Lemon juice Classic Coke2.5 Coffee5.0 Pure Water7.0 Blood Milk of Magnesia 10.5 Household ammonia M NaOH 14.0 Substance pH 1 M HCl0.0 Gastric juices Lemon juice Classic Coke2.5 Coffee5.0 Pure Water7.0 Blood Milk of Magnesia 10.5 Household ammonia M NaOH 14.0

16-26 CHEM 102, Fall 2010, LA TECH pH of 0.5 M H 2 SO 4 Solution H 2 SO 4 (aq) + H 2 O(l) H 3 + O(aq) + HSO 4 - (aq ) H 2 SO 4 (aq) + H 2 O(l) H 3 + O(aq) + HSO 4 - (aq ) HSO 4 - (aq ) + H 2 O(l) H 3 + O(aq) + SO 4 2- (aq ) HSO 4 - (aq ) + H 2 O(l) H 3 + O(aq) + SO 4 2- (aq ) [H 3 + O][HSO 4 - ] [H 3 + O][HSO 4 - ] H 2 SO 4 ; K a1 = H 2 SO 4 ; K a1 = [H 2 SO 4 ] [H 2 SO 4 ] [H 3 + O][ SO 4 2- ] [H 3 + O][ SO 4 2- ] H 2 SO 4 ; K a2 = ; K a2 ignored H 2 SO 4 ; K a2 = ; K a2 ignored [HSO 4 - ] [HSO 4 - ]

16-27 CHEM 102, Fall 2010, LA TECH H2SO4(aq) + H2O(l) H3 + O(aq) + HSO4 - (aq ) the moles of H + ions in the solution is equal to moles of H2SO4 at the beginning. [H2SO4] = [H + ] = 0.5 mole/L pH = -log [H + ] pH = -log(0.5) pH = 0.30 pH of 0.5 M H 2 SO 4 Solution

16-28 CHEM 102, Fall 2010, LA TECH 1.5 x M NaOH. NaOH is also a strong base dissociates completely in water. NaOH is also a strong base dissociates completely in water. [NaOH] = [HO - ] = 1.5 x mole/L [NaOH] = [HO - ] = 1.5 x mole/L pOH = -log[HO - ]= -log(1.5 x ) pOH = -log[HO - ]= -log(1.5 x ) pOH = 1.82 pOH = 1.82 As defined and derived previously: As defined and derived previously: pK w = pH + pOH; pK w = 14 pH = pK w + pOH pH = 14 - pOH pH = ; pH = 12.18

16-29 CHEM 102, Fall 2010, LA TECH Mixtures of Strong and Weak Acids the presence of the strong acid retards the dissociation of the weak acid

16-30 CHEM 102, Fall 2010, LA TECH Measuring pH Arnold Beckman inventor of the pH meter father of electronic instrumentation

16-31 CHEM 102, Fall 2010, LA TECH Equilibrium, Constant, K a & K b K a : Acid dissociation constant for a equilibrium reaction. K b : Base dissociation constant for a equilibrium reaction. Acid: HA + H 2 O H 3 + O + A - Base: BOH + H 2 O B + + OH - [H 3 + O][ A - ] [B + ][OH - ] K a = ; K b = [HA] [BOH]

16-32 CHEM 102, Fall 2010, LA TECH HCl(aq) + H 2 O(l) H 3 + O(aq) + Cl - (aq) HCl(aq) + H 2 O(l) H 3 + O(aq) + Cl - (aq) [H 3 + O][Cl-] [H 3 + O][Cl-] K a = [HCl] [HCl] [H + ][Cl-] [H + ][Cl-] K a = [HCl] [HCl] Acid Dissociation Constant

16-33 CHEM 102, Fall 2010, LA TECH Base Dissociation Constant NH 3 + H 2 O NH OH - [NH 4 + ][OH - ] K = [NH 3 ]

16-34 CHEM 102, Fall 2010, LA TECH Hydrated Metal Ions as Acids

16-35 CHEM 102, Fall 2010, LA TECH Ionization Constants for Acids

16-36 CHEM 102, Fall 2010, LA TECH Comparing K w and K a & K b Any compound with a K a value greater than K w of water will be a an acid in water. Any compound with a K b value greater than K w of water will be a base in water.

16-37 CHEM 102, Fall 2010, LA TECH WEAKER/STRONGER Acids and Bases & K a and K b values A larger value of K a or K b indicates an equilibrium favoring product side. Acidity and basicity increase with increasing K a or K b. Acidity and basicity increase with increasing K a or K b. pK a = - log K a and pK b = - log K b Acidity and basicity decrease with increasing pK a or pK b.

16-38 CHEM 102, Fall 2010, LA TECH Which is weaker? a. HNO 2 ; K a = 4.0 x b. HOCl 2 ; K a = 1.2 x c. HOCl ; K a = 3.5 x d. HCN ; K a = 4.9 x

16-39 CHEM 102, Fall 2010, LA TECH What is K a1 and K a2 ? H 2 SO 4 (aq) + H 2 O(l) H 3 + O(aq) + HSO 4 - (aq) HSO 4 - (aq) + H 2 O(l) H 3 + O(aq) + SO 4 2- (aq)

16-40 CHEM 102, Fall 2010, LA TECH H 2 SO 4 (aq) + H 2 O(l) H 3 + O(aq) + HSO 4 - (aq ) HSO 4 - (aq ) + H 2 O(l) H 3 + O(aq) + SO 4 2- (aq ) [H 3 + O][HSO 4 - ] [H 3 + O][HSO 4 - ] H 2 SO 4 ; K a1 = [H 2 SO 4 ] [H 2 SO 4 ] [H 3 + O][SO 4 2- ] H 2 SO 4 ; K a2 = [HSO 4 - ] [HSO 4 - ] K a Examples

16-41 CHEM 102, Fall 2010, LA TECH HC 2 H 3 O 2 (aq) + H 2 O(l) H 3 + O(aq) + C 2 H 3 O 2 - (aq) [H + ][C 2 H 3 O 2 - ] [H + ][C 2 H 3 O 2 - ] H C 2 H 3 O 2 ; K a = H C 2 H 3 O 2 ; K a = [H C 2 H 3 O 2 ] [H C 2 H 3 O 2 ] NH 3 (aq) + H 2 O(l) NH OH - (aq) [NH 4 + ][OH - ] [NH 4 + ][OH - ] NH 3 ; K b = NH 3 ; K b = [ NH 3 ] [ NH 3 ] K a Examples

16-42 CHEM 102, Fall 2010, LA TECH How do you calculate pH of weak acids/bases From % dissociation From K a or K b What is % dissociation Amount dissociated Amount dissociated % Dissoc. = x 100 Initial amount Initial amount

16-43 CHEM 102, Fall 2010, LA TECH How do you calculate % dissociation from K a or K b 1.00 M solution of HCN; K a = 4.9 x What is the % dissociation for the acid?

16-44 CHEM 102, Fall 2010, LA TECH 1.00 M solution of HCN; K a = 4.9 x First write the dissociation equilibrium equation: First write the dissociation equilibrium equation: HCN(aq) + H 2 O(l) H 3 + O(aq) + CN - (aq) [HCN] [H + ] [CN - ] [HCN] [H + ] [CN - ] Ini. Con M 0.0 M 0.00 M Cha. Con -x x x Eq. Con x x x [H 3 + O ][CN - ] x 2 [H 3 + O ][CN - ] x 2 K a = = K a = = [HCN] x [HCN] x 1.00 M solution of HCN; K a = 4.9 x

16-45 CHEM 102, Fall 2010, LA TECH x ~ 1.00 since x is small x 2 x 2 K a = ; K a =4.9 x = x 2 K a = ; K a =4.9 x = x x = 4.9 x = 2.21 x x = 4.9 x = 2.21 x Amount disso x x 100 = x 100 Ini. amount 1.00 Ini. amount 1.00 % Diss.=2.21 x x 100 = % % Diss.=2.21 x x 100 = % 1.00 M solution of HCN; K a = 4.9 x

16-46 CHEM 102, Fall 2010, LA TECH % Dissociation gives x (amount dissociated) need for pH calculation Amount dissociated Amount dissociated % Dissoc. = x 100 Initial amount/con. Initial amount/con. x % Dissoc. = x 100 % Dissoc. = x 100 concentration concentration

16-47 CHEM 102, Fall 2010, LA TECH 1 M HF, 2.7% dissociated Notice the conversion of % dissociation to a fraction (x): 2.7/100=0.027) x=0.027 Calculate the pH of a weak acid from % dissociation

16-48 CHEM 102, Fall 2010, LA TECH HF(aq) + H 2 O(l) H 3 + O(aq) + F - (aq) [H + ][F - ] [H + ][F - ] K a = [HF] [HF] [HF] [H + ] [F - ] [HF] [H + ] [F - ] Ini. Con M 0.0 M0.00 M Chg. Con -x x x Eq.Con pH = -log [H + ] pH = -log [H + ] pH = -log(0.027) pH = -log(0.027) pH = 1.57 pH = 1.57 Calculate the pH of a weak acid from % dissociation

16-49 CHEM 102, Fall 2010, LA TECH Weak acid Equilibria Example Determine the pH of a 0.10 M benzoic acid solution at 25 o C if K a = 6.28 x HBz (aq) + H 2 O (l) H 3 O + (aq) + Bz -(aq) The first step is to write the equilibrium expression K a = K a = [H 3 O + ][Bz - ] [HBz]

16-50 CHEM 102, Fall 2010, LA TECH Weak acid Equilibria HBz H 3 O + Bz - HBz H 3 O + Bz - Initial conc., M Change,  M -x x x Eq. Conc., M x x x [H 3 O + ] = [Bz - ] = x We’ll assume that [Bz - ] is negligible compared to [HBz]. The contribution of H 3 O + from water is also negligible.

16-51 CHEM 102, Fall 2010, LA TECH Weak Acid Equilibria Solve the equilibrium equation in terms of x K a = 6.28 x = x = (6.28 x )(0.10) H 3 O + = M H 3 O + = M pH= 2.60 x

16-52 CHEM 102, Fall 2010, LA TECH pH from K a or K b 1.00 M solution of HCN; K a = 4.9 x First write the dissociation equilibrium equation: First write the dissociation equilibrium equation: HCN(aq) + H 2 O(l) H 3 + O(aq) + CN - (aq) [HCN] [H + ] [CN - ] [HCN] [H + ] [CN - ] Ini. Con M 0.0 M 0.00 M Chg. Con -x x x Eq. Con x x x

16-53 CHEM 102, Fall 2010, LA TECH [H 3 + O ][CN - ] x 2 [H 3 + O ][CN - ] x 2 K a = = K a = = [HCN] x [HCN] x x ~ 1.00 since x is small x ~ 1.00 since x is small x 2 x 2 K a = ; K a =4.9 x = x 2 K a = ; K a =4.9 x = x x = 4.9 x = 2.21 x x = 4.9 x = 2.21 x pH = -log [H + ] pH = -log [H + ] pH = -log(2.21 x ) pH = -log(2.21 x ) pH = 4.65 pH = 4.65 Weak Acid Equilibria

16-54 CHEM 102, Fall 2010, LA TECH The Conjugate Partners of Strong Acids and Bases The conjugate acid/base of a strong base/acid has no net effect on the pH of a solution The conjugate base of a weak acid hydrolyze in water and basic or pH of a solution > 7.00 E.g. Na + C 2 H 3 O 2 - sodium acetate The conjugate acid of a weak base hydrolyze in water and acidic or pH of a solution < 7.00 E.g NH 4 Cl

16-55 CHEM 102, Fall 2010, LA TECH Reaction of a basic anion or acidic cation with water is an ordinary Brønsted-Lowry acid-base reaction. CH3COO - (aq) + H2O (l) CH3COOH (aq) + OH - (aq) NH4 + (aq) + H2O (l) NH3 (aq) + H3O + (aq) This type of reaction is given a special name.Hydrolysis The reaction of an anion with water to produce the conjugate acid and OH -. The reaction of a cation with water to produce the conjugate base and H3O +.Hydrolysis

16-56 CHEM 102, Fall 2010, LA TECH Acid-Base Properties of Typical Ions

16-57 CHEM 102, Fall 2010, LA TECH What salt solutions would be acidic, basic and neutral? 1)strong acid + strong base = neutral 2)weak acid + strong base = basic 3)strong acid + weak base = acidic 4) weak acid + weak base = neutral, basic or an acidic solution depending on the relative strengths of the acid and the base. basic or an acidic solution depending on the relative strengths of the acid and the base.

16-58 CHEM 102, Fall 2010, LA TECH What pH? Neutral, basic or acidic? a)NaCla)NaCl neutral neutral b) NaC 2 H 3 O 2b) NaC 2 H 3 O 2 basic basic c) NaHSO 4c) NaHSO 4 acidic acidic d) NH 4 Cld) NH 4 Cl acidic acidic

16-59 CHEM 102, Fall 2010, LA TECH How do you calculate pH of a salt solution? Find out the pH, acidic or basic? If acidic it should be a salt of weak base If basic it should be a salt of weak acid if acidic calculate K a from K a = K w /K b if basic calculate K b from K b = K w /K a Do a calculation similar to pH of a weak acid or base

16-60 CHEM 102, Fall 2010, LA TECH What is the pH of 0.5 M NH 4 Cl salt solution? (NH 3 ; K b = 1.8 x ) Find out the pH, acidic if acidic calculate K a from K a = K w /K b K a = K w /K b = 1 x /1.8 x ) K a = X Do a calculation similar to pH of a weak acid

16-61 CHEM 102, Fall 2010, LA TECH Continued NH H 2 O H 3 + O + NH 3 NH H 2 O H 3 + O + NH 3 [NH 4 + ] [H 3 + O ] [NH 3 ] [NH 4 + ] [H 3 + O ] [NH 3 ] Ini. Con. 0.5 M 0.0 M0.00 M Change -x x x Eq. Con x x x [H 3 + O ] [NH 3 ] [H 3 + O ] [NH 3 ] K a (NH 4 + ) = = [NH 4 + ] [NH 4 + ] x 2 x ; appro.:0.5 - x. 0.5 (0.5 - x) (0.5 - x)

16-62 CHEM 102, Fall 2010, LA TECH x 2 x 2 K a (NH 4 + ) = = 5.56 x x 2 = 5.56 x x 0.5 = 2.78 x x 2 = 5.56 x x 0.5 = 2.78 x x= 2.78 x = 1.66 x [H + ] = x = 1.66 x M pH = -log [H + ] = - log 1.66 x pH = 4.77 pH of 0.5 M NH 4 Cl solution is 4.77 (acidic ) Continued

16-63 CHEM 102, Fall 2010, LA TECH Types of Acids and Bases Binary acids Oxyacid Organic acids Acidic oxides Basic oxides Amine Polyprotic acids

16-64 CHEM 102, Fall 2010, LA TECH Influence of Molecular Structure on Acid Strength Binary Hydrides hydrogen & one other element Bond Strengths weaker the bond, the stronger the acid Stability of Anion higher the electronegativity, stronger the acid

16-65 CHEM 102, Fall 2010, LA TECH Binary Acids Binary Acids Compounds containing acidic protons bonded to a more electronegative atom. e.g. HF, HCl, HBr, HI, H 2 S The acidity of the haloacid (HX; X = Cl, Br, I, F) Series increase in the following order: HF < HCl < HBr < HI HF < HCl < HBr < HI

16-66 CHEM 102, Fall 2010, LA TECH Oxyacids Oxyacids Compounds containing acidic - OH groups in the molecule. Acidity of H 2 SO 4 is greater than H 2 SO 3 because of the extra O (oxygens) The order of acidity of oxyacids from the a halogen (Cl, Br, or I) shows a similar trend. HClO 4 > HClO 3 > HClO 2 > HClO HClO 4 > HClO 3 > HClO 2 > HClO perchloric chloric chlorus hyphochlorus perchloric chloric chlorus hyphochlorus

16-67 CHEM 102, Fall 2010, LA TECH Influence of Molecular Structure on Acid Strength Oxyacids hydrogen, oxygen, & one other elementH-O-E higher the electronegativity on E, stronger the acid as this weakens the bond between the O and H

16-68 CHEM 102, Fall 2010, LA TECH <<< < Oxo Acid

16-69 CHEM 102, Fall 2010, LA TECH Acidic Oxides Acidic Oxides These are usually oxides of non-metallic elements such as P, S and N. E.g. NO 2, SO 2, SO 3, CO 2 E.g. NO 2, SO 2, SO 3, CO 2 They produce oxyacids when dissolved in water SO3 + H2O ---> H2SO4 CO2 + H2O ---> H2CO3 NO2 + H2O ---> HNO3

16-70 CHEM 102, Fall 2010, LA TECH Basic Oxides Basic Oxides Oxides oxides of metallic elements such as Na, K, Ca. They produce hydroxyl bases when dissolved in water. e.g. CaO + H 2 O ---> Ca(OH) 2 Na 2 O + H 2 O ---> 2 NaOH Na 2 O + H 2 O ---> 2 NaOH

16-71 CHEM 102, Fall 2010, LA TECH Protic Acids Monoprotic Acids: The form protic refers to acidity due to protons. Monoprotic acids have only one acidic proton. e.g. HCl. Polyprotic Acids: They have more than one acidic proton. e.g. H 2 SO 4 - diprotic acid H 3 PO 4 - triprotic acid.

16-72 CHEM 102, Fall 2010, LA TECH Polyprotic Acids acids where more than one hydrogen per molecule is released

16-73 CHEM 102, Fall 2010, LA TECH Polyprotic Acids

16-74 CHEM 102, Fall 2010, LA TECH Organic or Carboxylic Acids

16-75 CHEM 102, Fall 2010, LA TECH FCH 2 CO 2 H (strongest acid) > ClCH 2 CO 2 H > BrCH 2 CO 2 H (weakest acid). FCH 2 CO 2 H (strongest acid) > ClCH 2 CO 2 H > BrCH 2 CO 2 H (weakest acid). Acid K a pK a HCOOH (formic acid) 1.78 X CH 3 COOH (acetic acid) 1.74 X CH 3 CH 2 COOH (propanoic acid)1.38 x Organic or Carboxylic Acids

16-76 CHEM 102, Fall 2010, LA TECH Amines Amines Class of organic bases derived from ammonia NH 3 by replacing hydrogen by organic groups. They are defined as bases similar to NH 3 by Bronsted- Lowery or Lewis acid/base definitions.

16-77 CHEM 102, Fall 2010, LA TECH Amines

16-78 CHEM 102, Fall 2010, LA TECH Acid-Base Chemistry of Some Antacids

16-79 CHEM 102, Fall 2010, LA TECH Acid-Base in the Kitchen vinegar - acetic acid lemon juice (citrus juice) - citric acid baking soda - NaHCO 3 milk - lactic acid baking powder - H 2 PO 4 - & HCO 3 -

16-80 CHEM 102, Fall 2010, LA TECH Household Cleaners

16-81 CHEM 102, Fall 2010, LA TECH Dishwashing Detergent

16-82 CHEM 102, Fall 2010, LA TECH Lewis Definition G.N. Lewis was successful in including acid and bases without proton or hydroxyl ions. Lewis Acid: A substance that accepts an electron pair. Lewis base: A substance that donates an electron pair. E.g. BF 3 (g) + :NH 3 (g) F 3 B:NH 3 (s) the base donates a pair of electrons to the acid forming a coordinate covalent bond common to coordination compounds. Lewis acids/bases will be discussed later in detail

16-83 CHEM 102, Fall 2010, LA TECH Lewis Acids and Bases Reactions H + + NH 3     acid base acid base Cu NH 3  [Cu(NH 3 ) 4 +2 ] acid base acid base

16-84 CHEM 102, Fall 2010, LA TECH What acid base concepts (Arrhenius/Bronsted/Lewis) would best describe the following reactions: a) HCl(aq) + NaOH(aq) ---> NaCl(aq) + H 2 O(l) b)HCl(g) + NH 3 (g) --->NH 4 Cl(s) c)BF 3 (g) + NH 3 (g)--->F 3 B:NH 3 (s) d)Zn(OH) 2 (s) + 2OH - (aq) ---> [Zn(OH) 4 ] 2- (aq)