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Chapter 19
“Acids, Bases,
  and Salts”
Section 19.1
     Acid-Base Theories
 OBJECTIVES:

 –Define the properties of
  acids and bases.
Section 19.1
        Acid-Base Theories
   OBJECTIVES:
    –Compare and contrast
     acids and bases as defined
     by the theories of:
     a) Arrhenius,
     b) Brønsted-Lowry, and
     c) Lewis.
Properties of Acids
 They taste sour (don’t try this at home).
 They can conduct electricity.
   – Can be strong or weak electrolytes in
     aqueous solution
 React with metals to form H2 gas.
 Change the color of indicators
  (for example: blue litmus turns to red).
 React with bases (metallic hydroxides)
  to form water and a salt.
Properties of Acids
 They have a pH of less than 7 (more
  on this concept of pH in a later lesson)
 They react with carbonates and
  bicarbonates to produce a salt, water,
  and carbon dioxide gas
 How do you know if a chemical is an
  acid?
    – It usually starts with Hydrogen.
    – HCl, H2SO4, HNO3, etc. (but not water!)
Acids Affect Indicators, by
    changing their color




Blue litmus paper turns red in
contact with an acid (and red paper
stays red).
Acids
have a
  pH
less
than 7
Acids React with Active Metals


Acids react with active metals to
form salts and hydrogen gas:

HCl(aq) + Mg(s) → MgCl2(aq) + H2(g)

This is a single-replacement reaction
Acids React with Carbonates
       and Bicarbonates
     HCl + NaHCO3
Hydrochloric acid + sodium bicarbonate




      NaCl + H2O + CO2
  salt + water + carbon dioxide

An old-time home remedy for
 relieving an upset stomach
Effects of Acid Rain on Marble
        (marble is calcium carbonate)
George Washington:       George Washington:
 BEFORE acid rain         AFTER acid rain
Acids Neutralize Bases
  HCl + NaOH → NaCl + H2O
-Neutralization reactions
ALWAYS produce a salt (which is
an ionic compound) and water.
-Of course, it takes the right
proportion of acid and base to
produce a neutral salt
Sulfuric Acid = H2SO4
 Highestvolume
 production of any
 chemical in the U.S.
 (approximately 60 billion pounds/year)

 Used    in the production
  of paper
 Used in production of
  fertilizers
 Used in petroleum
  refining; auto batteries
Nitric Acid = HNO3
 Used   in the production
  of fertilizers
 Used in the production
  of explosives
 Nitric acid is a volatile
  acid – its reactive
  components evaporate
  easily
 Stains proteins yellow
  (including skin!)
Hydrochloric Acid = HCl
 Used   in the “pickling”
  of steel
 Used to purify
  magnesium from sea
  water
 Part of gastric juice, it
  aids in the digestion of
  proteins
 Sold commercially as
  Muriatic acid
Phosphoric Acid = H3PO4
        A  flavoring agent in
          sodas (adds “tart”)
         Used in the
          manufacture of
          detergents
         Used in the
          manufacture of
          fertilizers
         Not a common
          laboratory reagent
Acetic Acid = HC2H3O2
(also called Ethanoic Acid, CH3COOH)

 Used   in the
  manufacture of plastics
 Used in making
  pharmaceuticals
 Acetic acid is the acid
  that is present in
  household vinegar
Properties of Bases (metallic hydroxides)
 React   with acids to form water
  and a salt.
 Taste bitter.
 Feel slippery (don’t try this either).
 Can be strong or weak
  electrolytes in aqueous solution
 Change the color of indicators
  (red litmus turns blue).
Examples of Bases
        (metallic hydroxides)
 Sodium hydroxide, NaOH
    (lye for drain cleaner; soap)
 Potassium hydroxide,
 KOH (alkaline batteries)
 Magnesium hydroxide,
 Mg(OH)2 (Milk of Magnesia)
 Calcium hydroxide,
 Ca(OH)2 (lime; masonry)
Bases Affect Indicators




Red litmus paper
turns blue in contact
with a base (and blue   Phenolphthalein
paper stays blue).      turns purple in a
                        base.
Bases
have a
  pH
greater
than 7
Bases Neutralize Acids
Milk of Magnesia contains
magnesium hydroxide,
Mg(OH)2, which neutralizes
stomach acid, HCl.

  2 HCl + Mg(OH)2

                        Magnesium salts can cause
                        diarrhea (thus they are used
    MgCl2 + 2 H2O       as a laxative) and may also
                        cause kidney stones.
Acid-Base Theories
Svante Arrhenius
 He  was a Swedish chemist (1859-
  1927), and a Nobel prize winner in
  chemistry (1903)
 one of the first chemists to explain
  the chemical theory of the behavior
  of acids and bases
 Dr. Hubert Alyea (professor emeritus
  at Princeton University) was the last
  graduate student of Arrhenius.
Hubert N. Alyea (1903-1996)
1. Arrhenius Definition - 1887
 Acids produce hydrogen ions (H1+)
  in aqueous solution (HCl → H1+ + Cl1-)
 Bases produce hydroxide ions
  (OH1-) when dissolved in water.
            (NaOH → Na1+ + OH1-)
 Limitedto aqueous solutions.
 Only one kind of base (hydroxides)
 NH3 (ammonia) could not be an
  Arrhenius base: no OH1- produced.
Svante Arrhenius (1859-1927)
Polyprotic Acids?
 Some  compounds have more than
  one ionizable hydrogen to release
 HNO3 nitric acid - monoprotic
 H2SO4 sulfuric acid - diprotic - 2 H+
 H3PO4 phosphoric acid - triprotic - 3
  H+
 Having more than one ionizable
  hydrogen does not mean stronger!
Acids
 Not all compounds that have
  hydrogen are acids. Water?
 Also, not all the hydrogen in an
  acid may be released as ions
  –only those that have very polar
    bonds are ionizable - this is
    when the hydrogen is joined to
    a very electronegative element
Arrhenius examples...
 Consider  HCl = it is an acid!
 What about CH4 (methane)?
 CH3COOH (ethanoic acid, also
  called acetic acid) - it has 4
  hydrogens just like methane
  does…?
 Table 19.2, p. 589 for bases,
  which are metallic hydroxides
Organic Acids (those with carbon)
Organic acids all contain the carboxyl group,
(-COOH), sometimes several of them.
CH3COOH – of the 4 hydrogen, only 1 ionizable




         (due to being bonded to the highly electronegative Oxygen)



The carboxyl group is a poor proton donor, so
    ALL organic acids are weak acids.
2. Brønsted-Lowry - 1923
 A broader definition than Arrhenius
 Acid is hydrogen-ion donor (H+ or
  proton); base is hydrogen-ion acceptor.
 Acids and bases always come in pairs.
 HCl is an acid.
   – When it dissolves in water, it gives it’s
     proton to water.
    HCl(g) + H2O(l) ↔ H3O+(aq) + Cl-(aq)
 Water is a base; makes hydronium ion.
Johannes Brønsted   Thomas Lowry
   (1879-1947)       (1874-1936)
     Denmark           England
Why Ammonia is a Base
 Ammonia   can be explained as a
 base by using Brønsted-Lowry:
NH3(aq) + H2O(l) ↔ NH41+(aq) + OH1-(aq)
Ammonia is the hydrogen ion
 acceptor (base), and water is the
 hydrogen ion donor (acid).
This causes the OH1- concentration
 to be greater than in pure water,
 and the ammonia solution is basic
Acids and bases come in pairs
 A “conjugate base” is the remainder of
  the original acid, after it donates it’s
  hydrogen ion
 A “conjugate acid” is the particle
  formed when the original base gains a
  hydrogen ion
   Thus, a conjugate acid-base pair is related by
    the loss or gain of a single hydrogen ion.
   Chemical Indicators? They are weak
    acids or bases that have a different
    color from their original acid and base
Acids and bases come in pairs
   General equation is:
      HA(aq) + H2O(l) ↔ H3O+(aq) + A-(aq)
   Acid + Base ↔ Conjugate acid + Conjugate base
 NH3 + H2O ↔ NH41+ + OH1-
  base acid      c.a.   c.b.
 HCl + H2O ↔ H3O1+ + Cl1-
  acid base      c.a.   c.b.
 Amphoteric – a substance that can act as
  both an acid and base- as water shows
3. Lewis Acids and Bases
 GilbertLewis focused on the
  donation or acceptance of a pair of
  electrons during a reaction
 Lewis Acid - electron pair acceptor
 Lewis Base - electron pair donor
 Most general of all 3 definitions;
  acids don’t even need hydrogen!
 Summary: Table 19.4, page 592
Gilbert Lewis (1875-1946)
- Page 593
Section 19.2
 Hydrogen Ions and Acidity
 OBJECTIVES:

 –Describe how [H1+] and
  [OH1-] are related in an

  aqueous solution.
Section 19.2
 Hydrogen Ions and Acidity
 OBJECTIVES:

 –Classify a solution as
  neutral, acidic, or basic
  given the hydrogen-ion
  or hydroxide-ion
  concentration.
Section 19.2
 Hydrogen Ions and Acidity
 OBJECTIVES:

 –Convert hydrogen-ion
  concentrations into pH
  values and hydroxide-ion
  concentrations into pOH
  values.
Section 19.2
 Hydrogen Ions and Acidity
 OBJECTIVES:

 –Describe the purpose of
  an acid-base indicator.
Hydrogen Ions from Water
 Water ionizes, or falls apart into ions:
           H2O ↔ H1+ + OH1-
 Called the “self ionization” of water
 Occurs to a very small extent:
           [H1+ ] = [OH1-] = 1 x 10-7 M
 Since they are equal, a neutral solution
  results from water
       Kw = [H1+ ] x [OH1-] = 1 x 10-14 M2
   Kw is called the “ion product constant” for water
Ion Product Constant
 H2O ↔ H1+ + OH1-
 Kw is constant in every aqueous solution:
            [H+] x [OH-] = 1 x 10-14 M2
       +      -7           -
 If [H ] > 10 then [OH ] < 10
                                 -7
       +      -7           -
 If [H ] < 10 then [OH ] > 10
                                 -7

 If we know one, other can be determined
       +      -7                      -
 If [H ] > 10 , it is acidic and [OH ] < 10
                                            -7
       +      -7                      -
 If [H ] < 10 , it is basic and [OH ] > 10
                                             -7

   – Basic solutions also called “alkaline”
- Page 596
The pH concept – from 0 to 14
   pH = pouvoir hydrogene (Fr.)
        “hydrogen power”
 definition:    pH = -log[H+]
 in neutral pH = -log(1 x 10-7) = 7
 in acidic solution [H+] > 10-7
 pH < -log(10-7)
    – pH < 7 (from 0 to 7 is the acid range)
    – in base, pH > 7 (7 to 14 is base range)
Calculating pOH
 pOH = -log [OH-]
 [H+] x [OH-] = 1 x 10-14 M2
 pH + pOH = 14
 Thus, a solution with a pOH
  less than 7 is basic; with a
  pOH greater than 7 is an acid
 Not greatly used like pH is.
pH and Significant Figures
 For pH calculations, the hydrogen
  ion concentration is usually
  expressed in scientific notation
 [H1+] = 0.0010 M = 1.0 x 10-3 M,
  and 0.0010 has 2 significant figures
 the pH = 3.00, with the two
  numbers to the right of the decimal
  corresponding to the two significant
  figures
- Page 599
- Page 600
Measuring pH
 Why measure pH?
   Everyday solutions
    we use - everything
    from swimming pools,
    soil conditions for
    plants, medical
    diagnosis, soaps and
    shampoos, etc.
 Sometimes we can use
  indicators, other times
  we might need a pH
  meter
How to measure pH with wide-range paper




1. Moisten the pH
indicator paper strip
                        2.Compare the color
with a few drops of
                        to the chart on the vial
solution, by using a
                        – then read the pH
stirring rod.
                        value.
Some of the
  many pH
 Indicators
  and their
 pH range
Acid-Base Indicators
 Although  useful, there are limitations
 to indicators:
  –usually given for a certain
   temperature (25 oC), thus may
   change at different temperatures
  –what if the solution already has a
   color, like paint?
  – the ability of the human eye to
   distinguish colors is limited
Acid-Base Indicators
A pH meter may give more definitive
 results
  –some are large, others portable
  –works by measuring the voltage
   between two electrodes; typically
   accurate to within 0.01 pH unit of
   the true pH
  –Instruments need to be calibrated
  –Fig. 19.15, p.603
Section 19.3
Strengths of Acids and Bases
 OBJECTIVES:

 –Define strong acids and
  weak acids.
Section 19.3
Strengths of Acids and Bases
 OBJECTIVES:

 –Describe how an acid’s
  strength is related to the
  value of its acid
  dissociation constant.
Section 19.3
Strengths of Acids and Bases
 OBJECTIVES:

 –Calculate an acid
  dissociation constant
  (Ka) from concentration
  and pH measurements.
Section 19.3
Strengths of Acids and Bases
 OBJECTIVES:

 –Order acids by strength
  according to their acid
  dissociation constants
  (Ka).
Section 19.3
Strengths of Acids and Bases
 OBJECTIVES:

 –Order bases by strength
  according to their base
  dissociation constants
  (Kb).
Strength
   Acids and Bases are classified acording
    to the degree to which they ionize in
    water:
     – Strong are completely ionized in
       aqueous solution; this means they
       ionize 100 %
     – Weak ionize only slightly in aqueous
       solution
 Strength  is very different from
    Concentration
Strength
 Strong  – means it forms many
  ions when dissolved (100 %
  ionization)
 Mg(OH)2 is a strong base- it falls
  completely apart (nearly 100%
  when dissolved).
   –But, not much dissolves- so it
    is not concentrated
Strong Acid Dissociation
            (makes 100 % ions)
Weak Acid Dissociation
          (only partially ionizes)
Measuring strength
 Ionization is reversible:
           HA + H2O ↔ H+ + A-
                                  (Note that the arrow
 This makes an equilibrium goes both directions.)
 Acid dissociation constant = Ka
            +
 Ka = [H ][A ]
                 -    (Note that water is NOT shown,
                      because its concentration is
           [HA]       constant, and built into Ka)
 Stronger acid = more products (ions),
  thus a larger Ka (Table 19.7, page 607)
What about bases?
   Strong bases dissociate completely.
   MOH + H2O ↔ M+ + OH-      (M = a metal)
   Base dissociation constant = Kb
   Kb =    [M+ ][OH-]
              [MOH]
 Stronger    base = more dissociated
    ions are produced, thus a larger Kb.
Strength vs. Concentration
 The words concentrated and dilute tell
  how much of an acid or base is
  dissolved in solution - refers to the
  number of moles of acid or base in a
  given volume
 The words strong and weak refer to
  the extent of ionization of an acid or
  base
 Is a concentrated, weak acid possible?
Practice
   Write the Ka expression for HNO2
    1) Equation: HNO2 ↔ H1+ + NO21-
    2) Ka = [H1+] x [NO21-]
                [HNO2]

   Write the Kb expression for NH3
    (as NH4OH)
- Page 610
Section 19.4
  Neutralization Reactions
 OBJECTIVES:

 –Define the products of
  an acid-base reaction.
Section 19.4
  Neutralization Reactions
 OBJECTIVES:

 –Explain how acid-base
  titration is used to
  calculate the
  concentration of an acid
  or a base.
Section 19.4
  Neutralization Reactions
 OBJECTIVES:

 –Explain the concept of
  equivalence in
  neutralization reactions.
Section 19.4
  Neutralization Reactions
 OBJECTIVES:

 –Describe the relationship
  between equivalence
  point and the end point
  of a titration.
Acid-Base Reactions
 Acid   + Base  Water +
 Salt
 Propertiesrelated to every day:
  –antacids depend on neutralization
  –farmers adjust the soil pH
  –formation of cave stalactites
  –human body kidney stones from
   insoluble salts
Acid-Base Reactions
 NeutralizationReaction - a reaction
 in which an acid and a base react in
 an aqueous solution to produce a
 salt and water:
HCl(aq) + NaOH(aq)  NaCl(aq) + H2O(l)
H2SO4(aq) + 2KOH(aq)  K2SO4(aq) + 2H2O(l)
  – Table 19.9, page 613 lists some salts
Titration
 Titration
          is the process of adding a
  known amount of solution of known
  concentration to determine the
  concentration of another solution
 Remember? - a balanced equation is
  a mole ratio
 The equivalence point is when the moles
  of hydrogen ions is equal to the moles
  of hydroxide ions (= neutralized!)
- Page 614
Titration
 The concentration of acid (or base)
 in solution can be determined by
 performing a neutralization reaction
  –An indicator is used to show
   when neutralization has occurred
  –Often we use phenolphthalein-
   because it is colorless in neutral
   and acid; turns pink in base
Steps - Neutralization reaction
#1. A measured volume of acid of
 unknown concentration is added to
 a flask
#2. Several drops of indicator added
#3. A base of known concentration is
 slowly added, until the indicator
 changes color; measure the volume
  – Figure 19.22, page 615
Neutralization
 Thesolution of known
 concentration is called the
 standard solution
  – added by using a buret
 Continue
         adding until the indicator
 changes color
  – called the “end point” of the titration
  – Sample Problem 19.7, page 616
Section 19.5
      Salts in Solution
 OBJECTIVES:

 –Describe when a
  solution of a salt is acidic
  or basic.
Section 19.5
      Salts in Solution
 OBJECTIVES:

 –Demonstrate with
  equations how buffers
  resist changes in pH.
Salt Hydrolysis
A   salt is an ionic compound that:
   –comes from the anion of an acid
   –comes from the cation of a base
   –is formed from a neutralization
    reaction
   –some neutral; others acidic or basic
 “Salt hydrolysis” - a salt that reacts
  with water to produce an acid or base
Salt Hydrolysis
    Hydrolyzing salts usually come from:
    1. a strong acid + a weak base, or
    2. a weak acid + a strong base
    Strong refers to the degree of
     ionization
    A strong Acid + a strong Base = Neutral Salt
    How do you know if it’s strong?
    – Refer to the handout provided
      (downloadable from my web site)
Salt Hydrolysis
 Tosee if the resulting salt is
 acidic or basic, check the
 “parent” acid and base that
 formed it. Practice on these:
  HCl + NaOH NaCl, a neutral salt
  H2SO4 + NH4OH (NH ) SO , acidic salt
                          4 2   4


  CH3COOH + KOH  COOK, basic salt
                        CH 3
Buffers
 Buffers  are solutions in which the
 pH remains relatively constant,
 even when small amounts of acid
 or base are added
 –made from a pair of chemicals:
   a weak acid and one of it’s
   salts; or a weak base and one
   of it’s salts
Buffers
A  buffer system is better able to
  resist changes in pH than pure water
 Since it is a pair of chemicals:
   –one chemical neutralizes any acid
    added, while the other chemical
    would neutralize any additional
    base
   –AND, they produce each other
    in the process!!!
Buffers
 Example: Ethanoic (acetic) acid
  and sodium ethanoate (also
  called sodium acetate)
 Examples on page 621 of these
 The buffer capacity is the
  amount of acid or base that can
  be added before a significant
  change in pH
Buffers
 Thetwo buffers that are crucial to
 maintain the pH of human blood are:
 1. carbonic acid (H2CO3) & hydrogen
  carbonate (HCO31-)
  2. dihydrogen phosphate (H2PO41-) &
   monohydrogen phoshate (HPO42-)
  – Table 19.10, page 621 has some
    important buffer systems
  –Conceptual Problem 19.2, p. 622
Aspirin (which     Bufferin is
is a type of       one brand of
acid)              a buffered
sometimes          aspirin that
causes             is sold in
stomach            stores.
upset; thus by     What about
adding a           the cost
“buffer”, it       compared to
does not           plain
cause the          aspirin?
acid irritation.
Chemistry - Chp 19 - Acids, Bases, and Salt - PowerPoints

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Chemistry - Chp 19 - Acids, Bases, and Salt - PowerPoints

  • 2. Section 19.1 Acid-Base Theories  OBJECTIVES: –Define the properties of acids and bases.
  • 3. Section 19.1 Acid-Base Theories  OBJECTIVES: –Compare and contrast acids and bases as defined by the theories of: a) Arrhenius, b) Brønsted-Lowry, and c) Lewis.
  • 4. Properties of Acids  They taste sour (don’t try this at home).  They can conduct electricity. – Can be strong or weak electrolytes in aqueous solution  React with metals to form H2 gas.  Change the color of indicators (for example: blue litmus turns to red).  React with bases (metallic hydroxides) to form water and a salt.
  • 5. Properties of Acids  They have a pH of less than 7 (more on this concept of pH in a later lesson)  They react with carbonates and bicarbonates to produce a salt, water, and carbon dioxide gas  How do you know if a chemical is an acid? – It usually starts with Hydrogen. – HCl, H2SO4, HNO3, etc. (but not water!)
  • 6. Acids Affect Indicators, by changing their color Blue litmus paper turns red in contact with an acid (and red paper stays red).
  • 7. Acids have a pH less than 7
  • 8. Acids React with Active Metals Acids react with active metals to form salts and hydrogen gas: HCl(aq) + Mg(s) → MgCl2(aq) + H2(g) This is a single-replacement reaction
  • 9. Acids React with Carbonates and Bicarbonates HCl + NaHCO3 Hydrochloric acid + sodium bicarbonate NaCl + H2O + CO2 salt + water + carbon dioxide An old-time home remedy for relieving an upset stomach
  • 10. Effects of Acid Rain on Marble (marble is calcium carbonate) George Washington: George Washington: BEFORE acid rain AFTER acid rain
  • 11. Acids Neutralize Bases HCl + NaOH → NaCl + H2O -Neutralization reactions ALWAYS produce a salt (which is an ionic compound) and water. -Of course, it takes the right proportion of acid and base to produce a neutral salt
  • 12. Sulfuric Acid = H2SO4  Highestvolume production of any chemical in the U.S. (approximately 60 billion pounds/year)  Used in the production of paper  Used in production of fertilizers  Used in petroleum refining; auto batteries
  • 13. Nitric Acid = HNO3  Used in the production of fertilizers  Used in the production of explosives  Nitric acid is a volatile acid – its reactive components evaporate easily  Stains proteins yellow (including skin!)
  • 14. Hydrochloric Acid = HCl  Used in the “pickling” of steel  Used to purify magnesium from sea water  Part of gastric juice, it aids in the digestion of proteins  Sold commercially as Muriatic acid
  • 15. Phosphoric Acid = H3PO4 A flavoring agent in sodas (adds “tart”)  Used in the manufacture of detergents  Used in the manufacture of fertilizers  Not a common laboratory reagent
  • 16. Acetic Acid = HC2H3O2 (also called Ethanoic Acid, CH3COOH)  Used in the manufacture of plastics  Used in making pharmaceuticals  Acetic acid is the acid that is present in household vinegar
  • 17. Properties of Bases (metallic hydroxides)  React with acids to form water and a salt.  Taste bitter.  Feel slippery (don’t try this either).  Can be strong or weak electrolytes in aqueous solution  Change the color of indicators (red litmus turns blue).
  • 18. Examples of Bases (metallic hydroxides)  Sodium hydroxide, NaOH (lye for drain cleaner; soap)  Potassium hydroxide, KOH (alkaline batteries)  Magnesium hydroxide, Mg(OH)2 (Milk of Magnesia)  Calcium hydroxide, Ca(OH)2 (lime; masonry)
  • 19. Bases Affect Indicators Red litmus paper turns blue in contact with a base (and blue Phenolphthalein paper stays blue). turns purple in a base.
  • 20. Bases have a pH greater than 7
  • 21. Bases Neutralize Acids Milk of Magnesia contains magnesium hydroxide, Mg(OH)2, which neutralizes stomach acid, HCl. 2 HCl + Mg(OH)2 Magnesium salts can cause diarrhea (thus they are used MgCl2 + 2 H2O as a laxative) and may also cause kidney stones.
  • 23. Svante Arrhenius  He was a Swedish chemist (1859- 1927), and a Nobel prize winner in chemistry (1903)  one of the first chemists to explain the chemical theory of the behavior of acids and bases  Dr. Hubert Alyea (professor emeritus at Princeton University) was the last graduate student of Arrhenius.
  • 24. Hubert N. Alyea (1903-1996)
  • 25. 1. Arrhenius Definition - 1887  Acids produce hydrogen ions (H1+) in aqueous solution (HCl → H1+ + Cl1-)  Bases produce hydroxide ions (OH1-) when dissolved in water. (NaOH → Na1+ + OH1-)  Limitedto aqueous solutions.  Only one kind of base (hydroxides)  NH3 (ammonia) could not be an Arrhenius base: no OH1- produced.
  • 27. Polyprotic Acids?  Some compounds have more than one ionizable hydrogen to release  HNO3 nitric acid - monoprotic  H2SO4 sulfuric acid - diprotic - 2 H+  H3PO4 phosphoric acid - triprotic - 3 H+  Having more than one ionizable hydrogen does not mean stronger!
  • 28. Acids  Not all compounds that have hydrogen are acids. Water?  Also, not all the hydrogen in an acid may be released as ions –only those that have very polar bonds are ionizable - this is when the hydrogen is joined to a very electronegative element
  • 29. Arrhenius examples...  Consider HCl = it is an acid!  What about CH4 (methane)?  CH3COOH (ethanoic acid, also called acetic acid) - it has 4 hydrogens just like methane does…?  Table 19.2, p. 589 for bases, which are metallic hydroxides
  • 30. Organic Acids (those with carbon) Organic acids all contain the carboxyl group, (-COOH), sometimes several of them. CH3COOH – of the 4 hydrogen, only 1 ionizable (due to being bonded to the highly electronegative Oxygen) The carboxyl group is a poor proton donor, so ALL organic acids are weak acids.
  • 31. 2. Brønsted-Lowry - 1923  A broader definition than Arrhenius  Acid is hydrogen-ion donor (H+ or proton); base is hydrogen-ion acceptor.  Acids and bases always come in pairs.  HCl is an acid. – When it dissolves in water, it gives it’s proton to water. HCl(g) + H2O(l) ↔ H3O+(aq) + Cl-(aq)  Water is a base; makes hydronium ion.
  • 32. Johannes Brønsted Thomas Lowry (1879-1947) (1874-1936) Denmark England
  • 33. Why Ammonia is a Base  Ammonia can be explained as a base by using Brønsted-Lowry: NH3(aq) + H2O(l) ↔ NH41+(aq) + OH1-(aq) Ammonia is the hydrogen ion acceptor (base), and water is the hydrogen ion donor (acid). This causes the OH1- concentration to be greater than in pure water, and the ammonia solution is basic
  • 34. Acids and bases come in pairs  A “conjugate base” is the remainder of the original acid, after it donates it’s hydrogen ion  A “conjugate acid” is the particle formed when the original base gains a hydrogen ion  Thus, a conjugate acid-base pair is related by the loss or gain of a single hydrogen ion.  Chemical Indicators? They are weak acids or bases that have a different color from their original acid and base
  • 35. Acids and bases come in pairs  General equation is: HA(aq) + H2O(l) ↔ H3O+(aq) + A-(aq)  Acid + Base ↔ Conjugate acid + Conjugate base  NH3 + H2O ↔ NH41+ + OH1- base acid c.a. c.b.  HCl + H2O ↔ H3O1+ + Cl1- acid base c.a. c.b.  Amphoteric – a substance that can act as both an acid and base- as water shows
  • 36. 3. Lewis Acids and Bases  GilbertLewis focused on the donation or acceptance of a pair of electrons during a reaction  Lewis Acid - electron pair acceptor  Lewis Base - electron pair donor  Most general of all 3 definitions; acids don’t even need hydrogen!  Summary: Table 19.4, page 592
  • 39. Section 19.2 Hydrogen Ions and Acidity  OBJECTIVES: –Describe how [H1+] and [OH1-] are related in an aqueous solution.
  • 40. Section 19.2 Hydrogen Ions and Acidity  OBJECTIVES: –Classify a solution as neutral, acidic, or basic given the hydrogen-ion or hydroxide-ion concentration.
  • 41. Section 19.2 Hydrogen Ions and Acidity  OBJECTIVES: –Convert hydrogen-ion concentrations into pH values and hydroxide-ion concentrations into pOH values.
  • 42. Section 19.2 Hydrogen Ions and Acidity  OBJECTIVES: –Describe the purpose of an acid-base indicator.
  • 43. Hydrogen Ions from Water  Water ionizes, or falls apart into ions: H2O ↔ H1+ + OH1-  Called the “self ionization” of water  Occurs to a very small extent: [H1+ ] = [OH1-] = 1 x 10-7 M  Since they are equal, a neutral solution results from water Kw = [H1+ ] x [OH1-] = 1 x 10-14 M2  Kw is called the “ion product constant” for water
  • 44. Ion Product Constant  H2O ↔ H1+ + OH1-  Kw is constant in every aqueous solution: [H+] x [OH-] = 1 x 10-14 M2 + -7 -  If [H ] > 10 then [OH ] < 10 -7 + -7 -  If [H ] < 10 then [OH ] > 10 -7  If we know one, other can be determined + -7 -  If [H ] > 10 , it is acidic and [OH ] < 10 -7 + -7 -  If [H ] < 10 , it is basic and [OH ] > 10 -7 – Basic solutions also called “alkaline”
  • 46. The pH concept – from 0 to 14  pH = pouvoir hydrogene (Fr.) “hydrogen power”  definition: pH = -log[H+]  in neutral pH = -log(1 x 10-7) = 7  in acidic solution [H+] > 10-7  pH < -log(10-7) – pH < 7 (from 0 to 7 is the acid range) – in base, pH > 7 (7 to 14 is base range)
  • 47.
  • 48. Calculating pOH  pOH = -log [OH-]  [H+] x [OH-] = 1 x 10-14 M2  pH + pOH = 14  Thus, a solution with a pOH less than 7 is basic; with a pOH greater than 7 is an acid  Not greatly used like pH is.
  • 49. pH and Significant Figures  For pH calculations, the hydrogen ion concentration is usually expressed in scientific notation  [H1+] = 0.0010 M = 1.0 x 10-3 M, and 0.0010 has 2 significant figures  the pH = 3.00, with the two numbers to the right of the decimal corresponding to the two significant figures
  • 52. Measuring pH  Why measure pH? Everyday solutions we use - everything from swimming pools, soil conditions for plants, medical diagnosis, soaps and shampoos, etc.  Sometimes we can use indicators, other times we might need a pH meter
  • 53. How to measure pH with wide-range paper 1. Moisten the pH indicator paper strip 2.Compare the color with a few drops of to the chart on the vial solution, by using a – then read the pH stirring rod. value.
  • 54. Some of the many pH Indicators and their pH range
  • 55. Acid-Base Indicators  Although useful, there are limitations to indicators: –usually given for a certain temperature (25 oC), thus may change at different temperatures –what if the solution already has a color, like paint? – the ability of the human eye to distinguish colors is limited
  • 56. Acid-Base Indicators A pH meter may give more definitive results –some are large, others portable –works by measuring the voltage between two electrodes; typically accurate to within 0.01 pH unit of the true pH –Instruments need to be calibrated –Fig. 19.15, p.603
  • 57. Section 19.3 Strengths of Acids and Bases  OBJECTIVES: –Define strong acids and weak acids.
  • 58. Section 19.3 Strengths of Acids and Bases  OBJECTIVES: –Describe how an acid’s strength is related to the value of its acid dissociation constant.
  • 59. Section 19.3 Strengths of Acids and Bases  OBJECTIVES: –Calculate an acid dissociation constant (Ka) from concentration and pH measurements.
  • 60. Section 19.3 Strengths of Acids and Bases  OBJECTIVES: –Order acids by strength according to their acid dissociation constants (Ka).
  • 61. Section 19.3 Strengths of Acids and Bases  OBJECTIVES: –Order bases by strength according to their base dissociation constants (Kb).
  • 62. Strength  Acids and Bases are classified acording to the degree to which they ionize in water: – Strong are completely ionized in aqueous solution; this means they ionize 100 % – Weak ionize only slightly in aqueous solution  Strength is very different from Concentration
  • 63. Strength  Strong – means it forms many ions when dissolved (100 % ionization)  Mg(OH)2 is a strong base- it falls completely apart (nearly 100% when dissolved). –But, not much dissolves- so it is not concentrated
  • 64. Strong Acid Dissociation (makes 100 % ions)
  • 65. Weak Acid Dissociation (only partially ionizes)
  • 66. Measuring strength  Ionization is reversible: HA + H2O ↔ H+ + A- (Note that the arrow  This makes an equilibrium goes both directions.)  Acid dissociation constant = Ka +  Ka = [H ][A ] - (Note that water is NOT shown, because its concentration is [HA] constant, and built into Ka)  Stronger acid = more products (ions), thus a larger Ka (Table 19.7, page 607)
  • 67. What about bases?  Strong bases dissociate completely.  MOH + H2O ↔ M+ + OH- (M = a metal)  Base dissociation constant = Kb  Kb = [M+ ][OH-] [MOH]  Stronger base = more dissociated ions are produced, thus a larger Kb.
  • 68. Strength vs. Concentration  The words concentrated and dilute tell how much of an acid or base is dissolved in solution - refers to the number of moles of acid or base in a given volume  The words strong and weak refer to the extent of ionization of an acid or base  Is a concentrated, weak acid possible?
  • 69. Practice  Write the Ka expression for HNO2 1) Equation: HNO2 ↔ H1+ + NO21- 2) Ka = [H1+] x [NO21-] [HNO2]  Write the Kb expression for NH3 (as NH4OH)
  • 71. Section 19.4 Neutralization Reactions  OBJECTIVES: –Define the products of an acid-base reaction.
  • 72. Section 19.4 Neutralization Reactions  OBJECTIVES: –Explain how acid-base titration is used to calculate the concentration of an acid or a base.
  • 73. Section 19.4 Neutralization Reactions  OBJECTIVES: –Explain the concept of equivalence in neutralization reactions.
  • 74. Section 19.4 Neutralization Reactions  OBJECTIVES: –Describe the relationship between equivalence point and the end point of a titration.
  • 75. Acid-Base Reactions  Acid + Base  Water + Salt  Propertiesrelated to every day: –antacids depend on neutralization –farmers adjust the soil pH –formation of cave stalactites –human body kidney stones from insoluble salts
  • 76. Acid-Base Reactions  NeutralizationReaction - a reaction in which an acid and a base react in an aqueous solution to produce a salt and water: HCl(aq) + NaOH(aq)  NaCl(aq) + H2O(l) H2SO4(aq) + 2KOH(aq)  K2SO4(aq) + 2H2O(l) – Table 19.9, page 613 lists some salts
  • 77. Titration  Titration is the process of adding a known amount of solution of known concentration to determine the concentration of another solution  Remember? - a balanced equation is a mole ratio  The equivalence point is when the moles of hydrogen ions is equal to the moles of hydroxide ions (= neutralized!)
  • 79. Titration  The concentration of acid (or base) in solution can be determined by performing a neutralization reaction –An indicator is used to show when neutralization has occurred –Often we use phenolphthalein- because it is colorless in neutral and acid; turns pink in base
  • 80. Steps - Neutralization reaction #1. A measured volume of acid of unknown concentration is added to a flask #2. Several drops of indicator added #3. A base of known concentration is slowly added, until the indicator changes color; measure the volume – Figure 19.22, page 615
  • 81. Neutralization  Thesolution of known concentration is called the standard solution – added by using a buret  Continue adding until the indicator changes color – called the “end point” of the titration – Sample Problem 19.7, page 616
  • 82. Section 19.5 Salts in Solution  OBJECTIVES: –Describe when a solution of a salt is acidic or basic.
  • 83. Section 19.5 Salts in Solution  OBJECTIVES: –Demonstrate with equations how buffers resist changes in pH.
  • 84. Salt Hydrolysis A salt is an ionic compound that: –comes from the anion of an acid –comes from the cation of a base –is formed from a neutralization reaction –some neutral; others acidic or basic  “Salt hydrolysis” - a salt that reacts with water to produce an acid or base
  • 85. Salt Hydrolysis  Hydrolyzing salts usually come from: 1. a strong acid + a weak base, or 2. a weak acid + a strong base  Strong refers to the degree of ionization A strong Acid + a strong Base = Neutral Salt  How do you know if it’s strong? – Refer to the handout provided (downloadable from my web site)
  • 86. Salt Hydrolysis  Tosee if the resulting salt is acidic or basic, check the “parent” acid and base that formed it. Practice on these: HCl + NaOH NaCl, a neutral salt H2SO4 + NH4OH (NH ) SO , acidic salt 4 2 4 CH3COOH + KOH  COOK, basic salt CH 3
  • 87. Buffers  Buffers are solutions in which the pH remains relatively constant, even when small amounts of acid or base are added –made from a pair of chemicals: a weak acid and one of it’s salts; or a weak base and one of it’s salts
  • 88. Buffers A buffer system is better able to resist changes in pH than pure water  Since it is a pair of chemicals: –one chemical neutralizes any acid added, while the other chemical would neutralize any additional base –AND, they produce each other in the process!!!
  • 89. Buffers  Example: Ethanoic (acetic) acid and sodium ethanoate (also called sodium acetate)  Examples on page 621 of these  The buffer capacity is the amount of acid or base that can be added before a significant change in pH
  • 90. Buffers  Thetwo buffers that are crucial to maintain the pH of human blood are: 1. carbonic acid (H2CO3) & hydrogen carbonate (HCO31-) 2. dihydrogen phosphate (H2PO41-) & monohydrogen phoshate (HPO42-) – Table 19.10, page 621 has some important buffer systems –Conceptual Problem 19.2, p. 622
  • 91. Aspirin (which Bufferin is is a type of one brand of acid) a buffered sometimes aspirin that causes is sold in stomach stores. upset; thus by What about adding a the cost “buffer”, it compared to does not plain cause the aspirin? acid irritation.