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Chapter 19
Acids, Bases, and Salts
Acids and Bases


Acids
  • vinegar                  • citrus fruits
  • carbonated drinks        • car battery
  • lemon juice              • tea

Bases
  • calcium hydroxide in mortar     • antacids
  • household cleaning agents
Properties of Acids

1. Give foods a tart or sour taste
   a)lemon & vinegar for example
2. Aqueous solutions of acids are electrolytes
   (conduct electricity)
3. Acids cause certain chemical indicators to
   change color.
4. Acid + Base     Salt + water
Properties of Bases

1. Bases have a bitter taste
   a)soap
2. Bases have a slippery feel
3. Aqueous solutions of bases are electrolytes
   (conduct electricity)
4. Bases cause certain chemical indicators to
   change color.
5. Acid + Base    Salt + water
Arrhenius Acids & Bases
Chemists recognized the properties of acids and
bases, but were unable to propose a theory to
explain their behavior.
   In 1887, Swedish chemist Svante Arrhenius
  proposed a revolutionary way of defining and
         thinking about acids and bases
• Acids are hydrogen-containing compounds
  that ionize to yield hydrogen ions (H+) in
  aqueous solution.
• Bases are compounds that ionize to yield
  hydroxide ions (OH-) in aqueous solution
Arrhenius Acids
Monoprotic acids – acids that contain one
ionizable hydrogen
      HNO3 – nitric acid

Diprotic acids – acids that contain two ionizable
hydrogens
     H2SO4 – sulfuric acid


Triprotic acids – acids that contain three
ionizable hydrogens
      H3PO4 – phosphoric acid
Arrhenius Acids
• Not all compounds that contain hydrogen are
  acids
 Ex. CH4 – methane has weak polar C – H bonds
 and no ionizable hydrogens. Not an acid.

• Not all hydrogens in an acid may be released
  as hydrogen ions.

• Only hydrogens in very polar bonds are
  ionizable. In the case where hydrogen is joined
  to a very electronegative element.
        Ex. HCl hydrogen chloride very polar
        covalent molecule
Arrhenius Acids
• When HCL dissolves in water, it releases
  hydrogen ions because the hydrogen ions are
  stabilized by solvation.

                    H2O
   H – Cl (g)       H +
                          (aq)+ Cl- (aq)
   Hydrogen              Hydrogen    Chloride
   chloride                 ion       ion

   Ionizes to form an aqueous solution of hydronium
   ions and chloride ions

   HCl        +   H 2O      H 3O +    +    Cl-
Arrhenius Acids
• Ethanoic acid CH3COOH is a monoprotic acid due
  to its structure

            H     O

         H C      C O H

             H
The three H attached to the carbon are in weak polar
 bonds. They do not ionize.

Only the H bonded to the highly electronegative O can be
 ionized
Arrhenius Bases
Sodium hydroxide dissociates into sodium ions
and hydroxide ions in aqueous solution.
                  H2O
NaOH (s)          Na +
                         (aq)   + OH- (aq)
Sodium                 Sodium            Hydroxide
Hydroxide              Ion                 ion

 Potassium hydroxide dissociates into sodium
 ions and hydroxide ions in aqueous solution.
            H2O
 KOH (s)          K+ (aq) + OH- (aq)
 Potassium          Potassium          Hydroxide
 Hydroxide             Ion                ion
Arrhenius Bases

Group IA, the alkali metals, react with water to
produce solutions that are basic.

Group IA metals are very soluble in water and
can produce concentrated solutions.

Group 2A metals are not very soluble in water.
Their solutions are always very dilute.
Bronsted-Lowry Acids and Bases

Arrhenius’ definition of acids and bases is not a
very comprehensive one.

If defines acids and bases narrowly and does not
include certain substances that have acidic or
basic properties.
       Na2CO3 (aq) is basic
Bronsted-Lowry Acids and Bases

The Bronste-Lowry theory defines

     acid – a hydrogen-ion donor

     base – a hydrogen-ion acceptor

All acids and bases included in the Arrhenius
theory are also acids and bases according to the
Bronsted-Lowry theory.
Ammonia as a Base
         Bronsted-Lowry Theory
       NH3 (aq) + H2O (l)   NH4+ (aq)   + OH- (aq)

• ammonia is the hydrogen-ion acceptor and therefore a
  BL base

• water is the hydrogen-ion donor and therefore a BL
  acid.

• Hydrogen ions are transferred from water to ammonia,
  which causes the hydroxide-ion concentration to be
  greater than it is in pure water.
Conjugate Acids and Bases
      NH3 (aq) + H2O (l)      NH4+ (aq)     + OH- (aq)
     base       acid       conjugate acid   conjugate base



• When ammonia dissolves and reacts with water, NH4+
  is the conjugate acid of the base NH3.

• OH- is the conjugate base of acid H2O
Conjugate Acids and Bases

       HCl (g) + H2O (l) Ý      H3O+ (aq)     + Cl- (aq)
     acid       base         conjugate acid   conjugate base



• HCl is the hydrogen-ion donor – thus a BL acid.

• Water is the hydrogen-ion acceptor – thus BL base
Conjugate Acid-Base Pair
Conjugate acid – the particle formed when a base
 gains a hydrogen ion

Conjugate base – the particle that remains when an
 acid has donated a hydrogen ion..

Conjugate acids and bases are always paired with a
 base or an acid, respectively.

Conjugate acid-base pairs consists of two
 substances related by the loss or gain of a single
 hydrogen ion.
Common Conjugate Acid-Base Pairs
     Acid              Base
      HCl               Cl-
     H2SO4             HSO4-
     H 3O +             H 2O
     HSO4-             SO42-
    CH3COOH           CH3COO-
     H2CO3             HCO3-
     HCO3-             CO32-
     NH4+              NH3
     H 2O               OH-
Bronsted-Lowry Acids and Bases

A water molecule that gains a hydrogen ion
becomes a positively charged hydronium ion
(H3O+)

Amphoteric – a substance that can act as both
an acid and a base
      Ex: water

       H2SO4 + H2O       H3O+ + HSO4-
         NH3 + H2O       NH4+ + OH-
Lewis Acids and Bases

Gilbert Lewis proposed a third Acid Base theory

Acid – accepts a pair of electrons during a
reaction

Base – donates a pair of electrons during a
reaction

Concept is more general than either the
Arrhenius theory or the Bronsted-Lowry theory.
Lewis Acids and Bases

Lewis Acid – a substance that can accept a pair
of electrons to form a covalent bond.

Lewis Base – a substance that can donate a pair
of electrons to form a covalent bond.
                     ..
      H+      +   -:
                    O–H         O:
                                :

                   ..
                                H    H
      Lewis             Lewis
      Acid              Base
Acid Base Definitions
    Type             Acid           Base

  Arrhenius      H+ producer     OH- producer


Bronsted Lowry        H+         H+ acceptor

                 Electron-pair   Electron-pair
    Lewis          acceptor         donor
End of Section 19.1
Hydrogen Ions From Water

Water molecules are highly polar and are in
continuous motion.

Occasionally, the collisions between water
molecules are energetic enough to transfer a
hydrogen ion from one water molecule to
another.

Self ionization of water – the reaction in which
water molecules produce ions
Hydrogen Ions From Water
A water molecule that loses a hydrogen ion
becomes a negatively charged hydroxide ion

A water molecule that gains a hydrogen ion
becomes a positively charged hydronium ion

        H2O (l)     OH- (aq) +         H+ (aq)

                     Hydroxide ion   Hydroxide ion


Self ionization of water – the reaction in which
water molecules produce ions
Self Ionization of Water
Hydrogen ions in aqueous solution have several
names.

• Some chemists call them protons

•Some chemists call them hydrogen ions or
hydronium ions.

For our purposes, either H+ or H3O+ will represent
hydrogen ions in aqueous solution.

       H2O + H2O           H3O+   +   OH-
Self Ionization of Water
The self-ionization of water occurs to a very small
 extent.

• In pure water at 25˚C, the equilibrium
  concentration of hydrogen ions and hydroxide
  ions are each only 1 x 10-7.

• In other words the concentration of OH- and H+
  are equal in pure water
Neutral Solutions


Any aqueous solution in which H+ and OH-
 are equal is a neutral solution.
Ion Product Constant for Water
    When [H+] increases [OH-] decreases

    When [H+] decreases [OH-] increases

 LeChatelier’s principle – when a stress is
  applied to a system in dynamic equilibrium, the
  system changes in a way that relieves the stress

If additional ions (either H+ or OH-) are added to a
  solution, the equilibrium shifts. The concentration of
  the other type of ion decreases. More water
  molecules are formed in the process.

H+ (aq)   + OH- (aq)              H2O (l)
Ion Product Constant for Water
For aqueous solutions, the product of the
 hydrogen ion concentration and the hydroxide
 ion concentration equals 1.0 x 10-14

           [H+] x [OH-] = 1.0 x 10-14

   This equation is true for all dilute aqueous
               solutions at 25˚C.
Ion-Product Constant for Water (Kw) – the
 product of the concentrations of the hydrogen
 ions and hydroxide ions in water

                +         -             -14
Ion Product Constant for Water

           Not all solutions are neutral

When some substances dissolve in water, they
 release hydrogen ions.

When hydrogen chloride dissolves in water, it forms
 hydrochloric acid.
                  H2O

        HCl (g)          H+ (aq) + Cl- (aq)
Ion Product Constant for Water

In the previous HCl solution, the hydrogen-ion
 concentration is greater than the hydroxide-ion
 concentration.

Acidic Solution – one in which [H+] is greater than
 [OH-].


  The [H+] of an acidic solution is greater than 1 x 10-7
Ion Product Constant for Water

When sodium hydroxide dissolves in water, it forms
 hydroxide ions in solution.
                      H20

           NaOH(s)          Na+(aq) + OH-(aq)
In the above solution, the hydrogen-ion concentration
 is less than the hydroxide-ion concentration.
Basic Solution – one in which [H+] is less than [OH-]

   The [H+] of a basic solution is less than 1 x 10 -7

Basic solutions are also known as alkaline solutions.
                                           solutions
The pH Concept

The pH scale was proposed by Danish Scientist
 Soren Sorensen in 1909.

The pH scale is used to express [H+]

   1 2 3 4 5 6 7 8 9 10 11 12 13 14
Strongly            Neutral                 Strongly
Acidic                                       Basic
Calculating pH

The pH of a solution is the negative logarithm of the
 hydrogen-ion concentration.

                    pH = -log[H+]
Calculating pH

In neutral solution, the [H+] = 1 x 10-7M. The pH is 7

                    pH = -log[H+]
                  pH = -log(1 x 10-7)
                pH = -(log 1 + log 10-7)
                  pH = -(0.0 + -7.0)
                       pH = 7.0
Classifying Solutions

A solution in which [H+] is greater than 1 x 10-7 has a
 pH less than 7.0 and is acidic.

A solution in which [H+] is less than 1 x 10-7 has a pH
 greater than 7.0 and is basic.

The pH of pure water or a neutral aqueous solution is 7.0

Acidic solution:    pH < 7.0   [H+] > 1 x 10-7M
Neutral solution:   pH = 7.0   [H+] equals 1 x 10-7M
Basic solution:     pH > 7.0   [H+] < 1 x 10-7
Calculating pH

pH can be read from the value of [H+] if it is written in
 scientific notation and has a coefficient of 1.
Then the pH of the solution equals the exponent, with
 the sign changed from minus to plus

            [H+] = 1 x 10-2 has a pH of 2.0

           [H+] = 1 x 10-13 has a pH of 13.0
Calculating pH

If the pH is an integer, it is also possible to directly
  write the value of [H+].

             pH = 9.0 then [H+] of 1 x 10-9M

              pH = 4 then [H+] = 1 x 10-4M
Calculating pOH

The pOH of a solution equals the negative logarithm
 of the hydroxide-ion concentration
                     pOH = -log [OH-]

           A neutral solution has a pOH of 7

Acidic solution:    pOH > 7.0 [OH-] < 1 x 10-7M
Neutral solution:   pOH = 7.0 [OH-] equals 1 x 10-7M
Basic solution:     pOH < 7.0 [OH-] > 1 x 10-7
pH and pOH Relationship




  pOH + pH – 14

  pH= 14 – pOH

  pOH = 14 - pH
pH Significant Figures

For pH calculation, you should express the
 hydrogen-ion concentration in scientific
 notation

  [H+] = 0.0010M should be written 1.0 x 10-3


           0.0010M has two sig figs

Write pH = 3.00 with 2 zeros to the right of the
 decimal place representing the 2 sig figs
Problem Example
Colas are slightly acidic. If the [H+] in a solution
 is 1.0 X 10-5 M , is the solution acidic, basic or
 neutral. What is the [OH-] of this solution?

[H+] = 1.0 X 10-5 M which is greater than 1.0 X
 10-7 M so solution is acidic

         Kw = [OH-] x [H+] = 1.0 X 10-14

           [OH-] = 1.0 X 10-14 / [H+]
         [OH-] = 1.0 X 10-14 / 1.0 X 10-5
               [OH-] = 1.0 X 10-9
Problem Example
What is the pH of a solution with a hydrogen-
 ion concentration of 4.2 x 10-10 M?

                pH = -log [H+]
             pH = -log (4.2 x 10-10)
                pH = -(9.3765)
                  pH = 9.38
Problem Example

pH of an unknown solution is 6.35. What is its
 hydrogen-ion concentration?

                pH = -log [H+]
               6.35 = -log [H+]
               -6.35 = log [H+]
   Using calculator find the antilog of -6.35
              4.5 x 10-7 M = [H+]
Problem Example

What is the pH of a solution if the
[OH-] =4.0X10-11M?

           Kw = [H+] x [OH-]= 1 x 10-14
             [H+] = 1 x 10-14 / [OH-]
           [H+] = 1 x 10-14 / 4.0 x 10-11
               [H+] =0.25 x 10-3 M
               [H+] = 2.5 x 10-4 M
Problem Example (con’t)

What is the pH of a solution if the
[OH-] =4.0X10-11M?

                 pH = -log [H+]
              pH = -log (2.5 x 10-4)
                pH = - (-3.60205)
                   pH = 3.60
Acid-Base Indicators
Indicator - (HIn) is an acid or a base tht
 undergoes dissociation in a know pH range
An indicator is a valuable tool for measuring pH
 because its acid form and base form have
 different color in solution.
                                  OH-

         HIn (aq)        H+ (aq) +      In- (aq)
          acid                    H+    base
         form                            form

The acid form dominates the dissociation equilibrium at
 low pH (high [H+]), and the base form dominates the
 equilibrium at high pH (high [OH-])
Acid-Base Indicators


For each indicator, the change from dominating acid from to
 dominating base form occurs in a narrow range of
 approximately two pH units.

Within this range, the color of the solution is a mixture of the
 colors of the acid and the base forms.

Knowing the pH range over which this color change occurs,
 can give you a rough estimate of the pH of the solution.
Acid-Base Indicators
Many different indicators are needed to span the entire pH
 spectrum.
      Indicator characteristics that limit their usefulness.
• Listed pH values of indicators are usually given for 25ºC.
  At other temperatures, an indicator may change color at a
  different pH.
• If the solution being tested is not colorless, the color of the
  indicator may be distorted.
• Dissolved salts in a solution may also affect the indicator’s
  dissociation.
Using indicator strips can help overcome these problems.
pH Meters
        A pH meter makes rapid, accurate pH
                  measurements.

• often easier to use than liquid indicators or indicator
  strips.
• Measurements of pH obtained with a pH meter are
  typically accurate to within 0.01 pH unit of the true pH.
• Color and cloudiness of the unknown solution do not
  affect the accuracy of the pH value
• If the solution being tested is not colorless, the color
  of the indicator may be distorted.
End of section 19.2
Strong Acids
 Acids are classified as strong or weak depending
    on the degree to which they ionize in water.

• In general, strong acids are completely ionized in
 aqueous solution.
                  HNO3 - nitric acid
                  HCl - hydrochloric acid
                  H2SO4 - sulfuric acid
                  HClO4 - perchloric acid
                  HBr - hydrobromic acid
                  HI - hydroiodic acid

       HCl(g) + H2O(l)         H3O+(aq) + Cl-(aq)
Weak Acids
Weak acids ionize only slightly in aqueous solution.

• Some Weak Acids
     Acetic Acid                    H3COOH
     Boric Acid                     H3BO3 (all three are weak)
     Phosphoric Acid                H3PO4 (all three are weak)
     Sulfuric Acid                  HSO4- (first ionization is strong)

 CH3COOH(aq) + H2O(l)                 H3O+(aq) + CH3COO-
                             (aq)
    ethanoic acid    water             hydronium          ethanoate
                                           ion                 ion
Acid Strength

A strong acid completely dissociates in water
                ([H3O+] is high).


A weak acid remains largely undissociated.
              ([H3O+] is low).
Equilibrium Constant (Keq)
 Write the equilibrium-constant expression from the
             balanced chemical equation.

 CH3COOH(aq) + H2O(l)       H3O+(aq) + CH3COO-(aq)




Keq = [H3O+] x [ CH3COO- ]
       [H3COOH] x [H2O]     [H2O] constant in dilute solutions
Acid Dissociation Constant (Ka)
Ka = Ratio of the concentration of the dissociated
 form of an acid to the concentration of the
 undissociated form.


H3COOH(aq) + H2O(l)         H3O+(aq) + CH3COO-(aq)


Acid Dissociation Constant
             Ka = [H3O+] x [ CH3COO- ]
                      [CH3COOH]
Acid Dissociation Constant (Ka)
Acid dissociation constant reflects the fraction of an
 acid in the ionized form. (Ka sometimes called
 ionization constant)

If the value of the Ka is small, then the degree of
   dissociation or ionization of the acid in the solution
   is small.

Weak acids – small Ka values
Stronger the acid – larger the Ka
Acid Dissociation Constant (Ka)

Nitrous acid (HNO2) has a Ka of 4.4 x 10-4

Acetic acid (CH3COOH) has a Ka of 1.8 x 10-5

Nitrous acid is more ionized in solution and a
 stronger acid
Acids

Strong Acids
• Have high [H3O+]
• Large dissociation constant

Weak Acids
• Have low [H3O+]
• Small dissociation constant
Acids
Diprotic and triprotic acids lose their hydrogens one
 at a time.
Each ionization reaction has a separate dissociation
 constant.
H3PO4 – 3 separate dissociation constants.
Base Dissociation Constant (Kb)
Strong bases dissociate completely into metal ions
  and hydroxide ions in aqueous solution.
• Some strong bases are not very soluble in water
  (calcium hydroxide and magnesium hydroxide)
• Small amounts that do not dissolve dissociate
  completely

Weak bases react with water to form the hydroxide
 ion and the conjugate acid of the base.
      NH3(aq) + H2O(l)       NH4+(aq) + OH-(aq)
   Ammonia      Water       Ammonium Ion   Hydroxide ion
Base Dissociation Constant (Kb)
     NH3(aq) + H2O(l)        NH4+(aq) + OH-(aq)
   Ammonia     Water       Ammonium Ion             Hydroxide ion

   Only about 1% of ammonia is present as NH4+

Equilibrium Constant
  Keq = [NH4+] x [OH- ]
             [NH3] x [H2O]   [H2O] constant in dilute solutions


Base Dissociation Constant
                Kb = [NH4+] x [OH- ]
                          [NH3]
Concentration and Strength
The words concentrated and dilute indicate how
 much of an acid or base is dissolved in solution.
• Number of moles of the acid or base in a given volume

The words strong and weak refer to the extent of
 ionization or dissociation of an acid or base
• How many of the particles ionize or dissociate into ions

A sample of HCl added to a large volume of water
 becomes more dilute, but it is still a strong acid.

Vinegar is a dilute solution of a weak acid.
End of section 19.3
Acid-Base Reactions
If you mix a solution of a strong acid containing
   hydronium ions with a solution of a strong base that
   has an equal number of hydroxide ions, a neutral
   solution results.

• Final solution has properties that are characteristic of
  neither an acidic nor a basic solution.

      HCl(aq) + NaOH(aq)          NaCl(aq) + H2O(l)
    H2SO4(aq) + 2KOH(aq)           K2SO4(aq) + H2O(l)
Neutralization Reactions
Reactions of weak acids and weak bases do not
 usually produce a neutral solution.

In general, reactions with which an acid and a base
  react in an aqueous solution to produce a salt and
  water are called neutralization reactions.
                                  reactions
Making Salts
Prepare potassium chloride by mixing equal molar
 quantities of hydrochloric acid and potassium
 hydroxide.

            HCl + KOH          KCl + H20

Heating the solution to evaporate the water will leave
 the salt potassium chloride.

    In general, the reaction of an acid with a base
                 produced water and salt
Titration
The number of moles of hydrogen ions provided by
 the acid are equivalent to the number of hydroxide
 ions provided by the base.
     HCl(aq) + NaOH(aq)      NaCl (aq) + H20 (l)
     1 mole    1 mole        1 mole       1 mole

  H2SO4(aq) + 2NaOH(aq)      Na2SO4(aq) + 2H20 (l)
     1 mole    2 mole          1 mole       2 mole

When and acid & base are mixed, the Equivalence
 point is when the number of moles of hydrogen
 ions equals the number of moles of hydroxide ions.
Sample Problem
How many moles of sulfuric acid are required to
 neutralize 0.50 mol of sodium hydroxide?

  H2SO4(aq) + 2NaOH(aq)        Na2SO4(aq) + 2H20 (l)

• Mole ratio of H2SO4 to NaOH is 1:2



0.50 mol NaOH      1 mol H2SO4    =    0.25 mol H2SO4
                 2 mol NaOH
Practice Problem
How many moles of potassium hydroxide are needed
 to completely neutralize 1.56 mol of phosphoric
 acid?

   H3PO4(aq) + 3KOH(aq)        K3PO4(aq) + 3H2O(l)



1.56 mol H3PO4     3 mol KOH    =   4.68 mol H3PO4
                 1 mol H3PO4
Titration
You can determine the concentration of acid or base
 in a solution by performing a neutralization
 reaction.

You must use an appropriate acid-base indicator to
 show when neutralization has occurred.

In the lab, typically phenolphthalein for acid base
  neutralization reactions.

Solutions that contain phenolphthalein turn from
 colorless to deep pink as the pH of the solution
 changes from acidic to basic.
Titration




a. Measured volume of an acid solution of unknown
   concentration is added to a flask
Titration




b. Several drops of the indicator are added to the
   solution while the flask is swirled
Titration




c. Measured volumes of the base of known
   concentration are mixed into the acid until the
   indicator just barely changes color.
Titration

Titration – the process of adding a known amount of
  solution of known concentration to determine the
  concentration of another solution.

Standard solution – the solution of known
  concentration

End point – the point at which the indicator changes
 color

You can also use titration to find the concentration of
  a base using a standard acid.
Titration
Titration – the process of adding a known amount of
  solution of known concentration to determine the
  concentration of another solution.

Standard solution – the solution of known
  concentration

End point – the point at which the indicator changes
 color. The point of neutralization
Equivalence point – the point in a titration where the
 number of moles of hydrogen ions = number of
 moles of hydroxide ions..
Sample Problem
A 25ml solution of H2SO4 is completely neutralized by
 18ml of 1.0M NaOH. What is the concentration of
 the H2SO4 solution?

  H2SO4(aq) + 2NaOH(aq)       Na2SO4(aq) + 2H20 (l)

0.018 L NaOH 1.0 mol NaOH 1 mol H2SO4           =
            1L NaOH      2 mol NaOH 0.025L


                    0.36M H2SO4
Practice Problem
How many milliliters of 0.45M HCl will neutralize
 25.0ml of 1.00M KOH?

             HCl + KOH        H2O + KCl

0.025 L KOH 1.0 mol KOH  1 mol HCl
            1L KOH      1 mol KOH

   1 L HCl         1000 ml HCl     = 56 ml HCl
   0.45 mol HCl     1 L HCl
Practice Problem
What is the molarity of H3PO4 if 15.0 ml is completely
 neutralized by 38.5 ml of 0.150 M?

     H3PO4 + 3NaOH           3H2O + Na3PO4


0.0385 L NaOH 0.150 mol NaOH 1 mol H3PO4
             1L NaOH        3 mol NaOH

                    = 0.129M H3PO4
   0.015L H3PO4
End of section 19.4
Salt Hydrolysis

A salt consists of an anion from an acid and a cation
  from a base.

The salt forms as a result of a neutralization reaction

Although solutions of many salts are neutral, some
  are acidic and others are basic.

..
Salt Hydrolysis
Salt Hydrolysis – the cations or anions of a
  dissociated salt remove hydrogen ions from or
  donate hydrogen ion to water.

Hydrolyzing salts are usually derived from a strong
 acid and weak base or from a weak acid and a
 strong base.

In general, salts that produce acidic solutions contain
  positive ions that release protons to water.

Salts that produce basic solutions contain negative
  ions that attract protons from water.
Salt Hydrolysis


CH3COONa (aq)            CH3COO- (aq) +       Na+ (aq)
Sodium ethanoate            ethanoate ion     sodium ion



CH3COONa is the salt from a weak acid CH3COOH
 and a strong base NaOH

In solution the salt is completely ionized.
Salt Hydrolysis
Salt Hydrolysis – the cations or anions of a
  dissociated salt remove hydrogen ions from or
  donate hydrogen ion to water.

CH3COO-(aq) + H2O(l)           CH3COOH (aq) + OH- (aq)
  BL base         BL acid                            makes
 hydrogen-ion   hydrogen-ion                        solution
  acceptor        donor                               basic

This process is called hydrolysis because it splits a
  hydrogen ion off a water molecule.
Resulting solution contains a hydroxide-ion concentration
  greater than the hydrogen-ion concentration. Thus
  the solution is basic
Salt Hydrolysis
        NH4Cl (aq)        NH4+ (aq) +   Cl- (aq)
       Ammonium          Ammonium ion   Chloride ion
        chloride



NH4Cl is the salt from a strong acid (hydrochloric
 acid, HCl) and a weak base (ammonia, NH3)


      In solution the salt is completely ionized.
Salt Hydrolysis

      NH4+(aq) + H2O(l)         NH3(aq) + H3O+(aq)
  BL acid        BL base                     makes
 hydrogen-ion   hydrogen-ion                 solution
  donor          acceptor                     acidic


This process is also called hydrolysis because it splits a
  hydrogen ion off a water molecule.

Resulting solution contains a hydrogen-ion concentration
  greater than the hydroxide-ion concentration. Thus
  the solution is acidic
Salt Hydrolysis
                 Equivalence Point
   Strong Acid
                      pH= 7          neutral
   Strong Base
   Weak Acid
                      pH > 7         basic
   Strong Base
   Strong Acid
                      pH < 7         acidic
   Weak Base

Equivalence point – the point in a titration where
the number of moles of hydrogen ions = number of
moles of hydroxide ions
Buffers


Buffer – a solution in which the pH remains relatively
  constant when small amounts of acid or base are
  added.

A buffer is a solution of a weak acid and one of its salts,
  or a solution of a weak base and one of its salts.

A buffer solution is better able to resist drastic changes in
  pH than is pure water.
Buffers

A solution of ethanoic acid (CH3COOH) and sodium
  ethanoate (CH3COONa) is an example of a typical
  buffer.


CH3COOH and CH3COO- (source is the completely
 ionized CH3COONa) act as reservoirs of neutralizing
 power.
Buffers

      CH3COO-(aq) + H+(aq)                    CH3COOH (aq)
      ethanoate ion         hydrogen ion          ethanoic acid


When an acid is added to the solution, the ethanoate
 ions act as a hydrogen-ion sponge.

CH3COOH (aq) + OH-(aq)                 CH3COO-(aq) + H2O (l)
Ethanoic acid         hydroxide ion        ethanoate ion      water


When a base is added to the solution, the ethanoic
 acid and the hydroxide ions react to produce water
 and the ethanoate ion.
Buffers

The ethanoate ion is not strong enough base to
  accept hydrogen ions from water extensively.

The buffer solution cannot control the pH when too
  much acid is added, because no more ethanoate
  ions are present to accept hydrogen ions.

Buffer also become ineffective when too much base
  is added. No more ethanoic acid molecules are
  present to donate hydrogen ions.
Buffers

When too much acid or base is added, the buffer
 capacity is exceeded.

Buffer capacity – the amount of acid or base than
 can be added to a buffer solution before a
 significant change in pH occurs.
Buffers


When a base is added to a buffered solution,
 the acidic form removes hydroxide ions from
 the solution.

When an acid is added to a buffered solution,
 the basic form removes hydrogen ions from
 the solution.
Buffers & Your Blood
Your body function properly only when the pH of
  your blood lies between 7.35 and 7.45.

Your blood contains buffers (hydrogen carbonate
  ions and carbonic acid)

   HCO3- (aq)      +    H+ (aq)         H2CO3 (aq)
    hydrogen           hydrogen ions   carbonic acid
   carbonate ion

As long as there are hydrogen carbonate ions
  available, the excess hydrogen ions are removed,
  and the pH of the blood changes very little.
End of Section Chapter 19

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Chapter 19

  • 2. Acids and Bases Acids • vinegar • citrus fruits • carbonated drinks • car battery • lemon juice • tea Bases • calcium hydroxide in mortar • antacids • household cleaning agents
  • 3. Properties of Acids 1. Give foods a tart or sour taste a)lemon & vinegar for example 2. Aqueous solutions of acids are electrolytes (conduct electricity) 3. Acids cause certain chemical indicators to change color. 4. Acid + Base Salt + water
  • 4. Properties of Bases 1. Bases have a bitter taste a)soap 2. Bases have a slippery feel 3. Aqueous solutions of bases are electrolytes (conduct electricity) 4. Bases cause certain chemical indicators to change color. 5. Acid + Base Salt + water
  • 5. Arrhenius Acids & Bases Chemists recognized the properties of acids and bases, but were unable to propose a theory to explain their behavior. In 1887, Swedish chemist Svante Arrhenius proposed a revolutionary way of defining and thinking about acids and bases • Acids are hydrogen-containing compounds that ionize to yield hydrogen ions (H+) in aqueous solution. • Bases are compounds that ionize to yield hydroxide ions (OH-) in aqueous solution
  • 6. Arrhenius Acids Monoprotic acids – acids that contain one ionizable hydrogen HNO3 – nitric acid Diprotic acids – acids that contain two ionizable hydrogens H2SO4 – sulfuric acid Triprotic acids – acids that contain three ionizable hydrogens H3PO4 – phosphoric acid
  • 7. Arrhenius Acids • Not all compounds that contain hydrogen are acids Ex. CH4 – methane has weak polar C – H bonds and no ionizable hydrogens. Not an acid. • Not all hydrogens in an acid may be released as hydrogen ions. • Only hydrogens in very polar bonds are ionizable. In the case where hydrogen is joined to a very electronegative element. Ex. HCl hydrogen chloride very polar covalent molecule
  • 8. Arrhenius Acids • When HCL dissolves in water, it releases hydrogen ions because the hydrogen ions are stabilized by solvation. H2O H – Cl (g) H + (aq)+ Cl- (aq) Hydrogen Hydrogen Chloride chloride ion ion Ionizes to form an aqueous solution of hydronium ions and chloride ions HCl + H 2O H 3O + + Cl-
  • 9. Arrhenius Acids • Ethanoic acid CH3COOH is a monoprotic acid due to its structure H O H C C O H H The three H attached to the carbon are in weak polar bonds. They do not ionize. Only the H bonded to the highly electronegative O can be ionized
  • 10. Arrhenius Bases Sodium hydroxide dissociates into sodium ions and hydroxide ions in aqueous solution. H2O NaOH (s) Na + (aq) + OH- (aq) Sodium Sodium Hydroxide Hydroxide Ion ion Potassium hydroxide dissociates into sodium ions and hydroxide ions in aqueous solution. H2O KOH (s) K+ (aq) + OH- (aq) Potassium Potassium Hydroxide Hydroxide Ion ion
  • 11. Arrhenius Bases Group IA, the alkali metals, react with water to produce solutions that are basic. Group IA metals are very soluble in water and can produce concentrated solutions. Group 2A metals are not very soluble in water. Their solutions are always very dilute.
  • 12. Bronsted-Lowry Acids and Bases Arrhenius’ definition of acids and bases is not a very comprehensive one. If defines acids and bases narrowly and does not include certain substances that have acidic or basic properties. Na2CO3 (aq) is basic
  • 13. Bronsted-Lowry Acids and Bases The Bronste-Lowry theory defines acid – a hydrogen-ion donor base – a hydrogen-ion acceptor All acids and bases included in the Arrhenius theory are also acids and bases according to the Bronsted-Lowry theory.
  • 14. Ammonia as a Base Bronsted-Lowry Theory NH3 (aq) + H2O (l) NH4+ (aq) + OH- (aq) • ammonia is the hydrogen-ion acceptor and therefore a BL base • water is the hydrogen-ion donor and therefore a BL acid. • Hydrogen ions are transferred from water to ammonia, which causes the hydroxide-ion concentration to be greater than it is in pure water.
  • 15. Conjugate Acids and Bases NH3 (aq) + H2O (l) NH4+ (aq) + OH- (aq) base acid conjugate acid conjugate base • When ammonia dissolves and reacts with water, NH4+ is the conjugate acid of the base NH3. • OH- is the conjugate base of acid H2O
  • 16. Conjugate Acids and Bases HCl (g) + H2O (l) Ý H3O+ (aq) + Cl- (aq) acid base conjugate acid conjugate base • HCl is the hydrogen-ion donor – thus a BL acid. • Water is the hydrogen-ion acceptor – thus BL base
  • 17. Conjugate Acid-Base Pair Conjugate acid – the particle formed when a base gains a hydrogen ion Conjugate base – the particle that remains when an acid has donated a hydrogen ion.. Conjugate acids and bases are always paired with a base or an acid, respectively. Conjugate acid-base pairs consists of two substances related by the loss or gain of a single hydrogen ion.
  • 18. Common Conjugate Acid-Base Pairs Acid Base HCl Cl- H2SO4 HSO4- H 3O + H 2O HSO4- SO42- CH3COOH CH3COO- H2CO3 HCO3- HCO3- CO32- NH4+ NH3 H 2O OH-
  • 19. Bronsted-Lowry Acids and Bases A water molecule that gains a hydrogen ion becomes a positively charged hydronium ion (H3O+) Amphoteric – a substance that can act as both an acid and a base Ex: water H2SO4 + H2O H3O+ + HSO4- NH3 + H2O NH4+ + OH-
  • 20. Lewis Acids and Bases Gilbert Lewis proposed a third Acid Base theory Acid – accepts a pair of electrons during a reaction Base – donates a pair of electrons during a reaction Concept is more general than either the Arrhenius theory or the Bronsted-Lowry theory.
  • 21. Lewis Acids and Bases Lewis Acid – a substance that can accept a pair of electrons to form a covalent bond. Lewis Base – a substance that can donate a pair of electrons to form a covalent bond. .. H+ + -: O–H O: : .. H H Lewis Lewis Acid Base
  • 22. Acid Base Definitions Type Acid Base Arrhenius H+ producer OH- producer Bronsted Lowry H+ H+ acceptor Electron-pair Electron-pair Lewis acceptor donor
  • 24. Hydrogen Ions From Water Water molecules are highly polar and are in continuous motion. Occasionally, the collisions between water molecules are energetic enough to transfer a hydrogen ion from one water molecule to another. Self ionization of water – the reaction in which water molecules produce ions
  • 25. Hydrogen Ions From Water A water molecule that loses a hydrogen ion becomes a negatively charged hydroxide ion A water molecule that gains a hydrogen ion becomes a positively charged hydronium ion H2O (l) OH- (aq) + H+ (aq) Hydroxide ion Hydroxide ion Self ionization of water – the reaction in which water molecules produce ions
  • 26. Self Ionization of Water Hydrogen ions in aqueous solution have several names. • Some chemists call them protons •Some chemists call them hydrogen ions or hydronium ions. For our purposes, either H+ or H3O+ will represent hydrogen ions in aqueous solution. H2O + H2O H3O+ + OH-
  • 27. Self Ionization of Water The self-ionization of water occurs to a very small extent. • In pure water at 25˚C, the equilibrium concentration of hydrogen ions and hydroxide ions are each only 1 x 10-7. • In other words the concentration of OH- and H+ are equal in pure water
  • 28. Neutral Solutions Any aqueous solution in which H+ and OH- are equal is a neutral solution.
  • 29. Ion Product Constant for Water When [H+] increases [OH-] decreases When [H+] decreases [OH-] increases LeChatelier’s principle – when a stress is applied to a system in dynamic equilibrium, the system changes in a way that relieves the stress If additional ions (either H+ or OH-) are added to a solution, the equilibrium shifts. The concentration of the other type of ion decreases. More water molecules are formed in the process. H+ (aq) + OH- (aq) H2O (l)
  • 30. Ion Product Constant for Water For aqueous solutions, the product of the hydrogen ion concentration and the hydroxide ion concentration equals 1.0 x 10-14 [H+] x [OH-] = 1.0 x 10-14 This equation is true for all dilute aqueous solutions at 25˚C. Ion-Product Constant for Water (Kw) – the product of the concentrations of the hydrogen ions and hydroxide ions in water + - -14
  • 31. Ion Product Constant for Water Not all solutions are neutral When some substances dissolve in water, they release hydrogen ions. When hydrogen chloride dissolves in water, it forms hydrochloric acid. H2O HCl (g) H+ (aq) + Cl- (aq)
  • 32. Ion Product Constant for Water In the previous HCl solution, the hydrogen-ion concentration is greater than the hydroxide-ion concentration. Acidic Solution – one in which [H+] is greater than [OH-]. The [H+] of an acidic solution is greater than 1 x 10-7
  • 33. Ion Product Constant for Water When sodium hydroxide dissolves in water, it forms hydroxide ions in solution. H20 NaOH(s) Na+(aq) + OH-(aq) In the above solution, the hydrogen-ion concentration is less than the hydroxide-ion concentration. Basic Solution – one in which [H+] is less than [OH-] The [H+] of a basic solution is less than 1 x 10 -7 Basic solutions are also known as alkaline solutions. solutions
  • 34. The pH Concept The pH scale was proposed by Danish Scientist Soren Sorensen in 1909. The pH scale is used to express [H+] 1 2 3 4 5 6 7 8 9 10 11 12 13 14 Strongly Neutral Strongly Acidic Basic
  • 35. Calculating pH The pH of a solution is the negative logarithm of the hydrogen-ion concentration. pH = -log[H+]
  • 36. Calculating pH In neutral solution, the [H+] = 1 x 10-7M. The pH is 7 pH = -log[H+] pH = -log(1 x 10-7) pH = -(log 1 + log 10-7) pH = -(0.0 + -7.0) pH = 7.0
  • 37. Classifying Solutions A solution in which [H+] is greater than 1 x 10-7 has a pH less than 7.0 and is acidic. A solution in which [H+] is less than 1 x 10-7 has a pH greater than 7.0 and is basic. The pH of pure water or a neutral aqueous solution is 7.0 Acidic solution: pH < 7.0 [H+] > 1 x 10-7M Neutral solution: pH = 7.0 [H+] equals 1 x 10-7M Basic solution: pH > 7.0 [H+] < 1 x 10-7
  • 38.
  • 39. Calculating pH pH can be read from the value of [H+] if it is written in scientific notation and has a coefficient of 1. Then the pH of the solution equals the exponent, with the sign changed from minus to plus [H+] = 1 x 10-2 has a pH of 2.0 [H+] = 1 x 10-13 has a pH of 13.0
  • 40. Calculating pH If the pH is an integer, it is also possible to directly write the value of [H+]. pH = 9.0 then [H+] of 1 x 10-9M pH = 4 then [H+] = 1 x 10-4M
  • 41. Calculating pOH The pOH of a solution equals the negative logarithm of the hydroxide-ion concentration pOH = -log [OH-] A neutral solution has a pOH of 7 Acidic solution: pOH > 7.0 [OH-] < 1 x 10-7M Neutral solution: pOH = 7.0 [OH-] equals 1 x 10-7M Basic solution: pOH < 7.0 [OH-] > 1 x 10-7
  • 42. pH and pOH Relationship pOH + pH – 14 pH= 14 – pOH pOH = 14 - pH
  • 43.
  • 44. pH Significant Figures For pH calculation, you should express the hydrogen-ion concentration in scientific notation [H+] = 0.0010M should be written 1.0 x 10-3 0.0010M has two sig figs Write pH = 3.00 with 2 zeros to the right of the decimal place representing the 2 sig figs
  • 45. Problem Example Colas are slightly acidic. If the [H+] in a solution is 1.0 X 10-5 M , is the solution acidic, basic or neutral. What is the [OH-] of this solution? [H+] = 1.0 X 10-5 M which is greater than 1.0 X 10-7 M so solution is acidic Kw = [OH-] x [H+] = 1.0 X 10-14 [OH-] = 1.0 X 10-14 / [H+] [OH-] = 1.0 X 10-14 / 1.0 X 10-5 [OH-] = 1.0 X 10-9
  • 46. Problem Example What is the pH of a solution with a hydrogen- ion concentration of 4.2 x 10-10 M? pH = -log [H+] pH = -log (4.2 x 10-10) pH = -(9.3765) pH = 9.38
  • 47. Problem Example pH of an unknown solution is 6.35. What is its hydrogen-ion concentration? pH = -log [H+] 6.35 = -log [H+] -6.35 = log [H+] Using calculator find the antilog of -6.35 4.5 x 10-7 M = [H+]
  • 48. Problem Example What is the pH of a solution if the [OH-] =4.0X10-11M? Kw = [H+] x [OH-]= 1 x 10-14 [H+] = 1 x 10-14 / [OH-] [H+] = 1 x 10-14 / 4.0 x 10-11 [H+] =0.25 x 10-3 M [H+] = 2.5 x 10-4 M
  • 49. Problem Example (con’t) What is the pH of a solution if the [OH-] =4.0X10-11M? pH = -log [H+] pH = -log (2.5 x 10-4) pH = - (-3.60205) pH = 3.60
  • 50. Acid-Base Indicators Indicator - (HIn) is an acid or a base tht undergoes dissociation in a know pH range An indicator is a valuable tool for measuring pH because its acid form and base form have different color in solution. OH- HIn (aq) H+ (aq) + In- (aq) acid H+ base form form The acid form dominates the dissociation equilibrium at low pH (high [H+]), and the base form dominates the equilibrium at high pH (high [OH-])
  • 51. Acid-Base Indicators For each indicator, the change from dominating acid from to dominating base form occurs in a narrow range of approximately two pH units. Within this range, the color of the solution is a mixture of the colors of the acid and the base forms. Knowing the pH range over which this color change occurs, can give you a rough estimate of the pH of the solution.
  • 52. Acid-Base Indicators Many different indicators are needed to span the entire pH spectrum. Indicator characteristics that limit their usefulness. • Listed pH values of indicators are usually given for 25ºC. At other temperatures, an indicator may change color at a different pH. • If the solution being tested is not colorless, the color of the indicator may be distorted. • Dissolved salts in a solution may also affect the indicator’s dissociation. Using indicator strips can help overcome these problems.
  • 53.
  • 54. pH Meters A pH meter makes rapid, accurate pH measurements. • often easier to use than liquid indicators or indicator strips. • Measurements of pH obtained with a pH meter are typically accurate to within 0.01 pH unit of the true pH. • Color and cloudiness of the unknown solution do not affect the accuracy of the pH value • If the solution being tested is not colorless, the color of the indicator may be distorted.
  • 56. Strong Acids Acids are classified as strong or weak depending on the degree to which they ionize in water. • In general, strong acids are completely ionized in aqueous solution. HNO3 - nitric acid HCl - hydrochloric acid H2SO4 - sulfuric acid HClO4 - perchloric acid HBr - hydrobromic acid HI - hydroiodic acid HCl(g) + H2O(l) H3O+(aq) + Cl-(aq)
  • 57. Weak Acids Weak acids ionize only slightly in aqueous solution. • Some Weak Acids Acetic Acid H3COOH Boric Acid H3BO3 (all three are weak) Phosphoric Acid H3PO4 (all three are weak) Sulfuric Acid HSO4- (first ionization is strong) CH3COOH(aq) + H2O(l) H3O+(aq) + CH3COO- (aq) ethanoic acid water hydronium ethanoate ion ion
  • 58. Acid Strength A strong acid completely dissociates in water ([H3O+] is high). A weak acid remains largely undissociated. ([H3O+] is low).
  • 59. Equilibrium Constant (Keq) Write the equilibrium-constant expression from the balanced chemical equation. CH3COOH(aq) + H2O(l) H3O+(aq) + CH3COO-(aq) Keq = [H3O+] x [ CH3COO- ] [H3COOH] x [H2O] [H2O] constant in dilute solutions
  • 60. Acid Dissociation Constant (Ka) Ka = Ratio of the concentration of the dissociated form of an acid to the concentration of the undissociated form. H3COOH(aq) + H2O(l) H3O+(aq) + CH3COO-(aq) Acid Dissociation Constant Ka = [H3O+] x [ CH3COO- ] [CH3COOH]
  • 61. Acid Dissociation Constant (Ka) Acid dissociation constant reflects the fraction of an acid in the ionized form. (Ka sometimes called ionization constant) If the value of the Ka is small, then the degree of dissociation or ionization of the acid in the solution is small. Weak acids – small Ka values Stronger the acid – larger the Ka
  • 62. Acid Dissociation Constant (Ka) Nitrous acid (HNO2) has a Ka of 4.4 x 10-4 Acetic acid (CH3COOH) has a Ka of 1.8 x 10-5 Nitrous acid is more ionized in solution and a stronger acid
  • 63. Acids Strong Acids • Have high [H3O+] • Large dissociation constant Weak Acids • Have low [H3O+] • Small dissociation constant
  • 64. Acids Diprotic and triprotic acids lose their hydrogens one at a time. Each ionization reaction has a separate dissociation constant. H3PO4 – 3 separate dissociation constants.
  • 65. Base Dissociation Constant (Kb) Strong bases dissociate completely into metal ions and hydroxide ions in aqueous solution. • Some strong bases are not very soluble in water (calcium hydroxide and magnesium hydroxide) • Small amounts that do not dissolve dissociate completely Weak bases react with water to form the hydroxide ion and the conjugate acid of the base. NH3(aq) + H2O(l) NH4+(aq) + OH-(aq) Ammonia Water Ammonium Ion Hydroxide ion
  • 66. Base Dissociation Constant (Kb) NH3(aq) + H2O(l) NH4+(aq) + OH-(aq) Ammonia Water Ammonium Ion Hydroxide ion Only about 1% of ammonia is present as NH4+ Equilibrium Constant Keq = [NH4+] x [OH- ] [NH3] x [H2O] [H2O] constant in dilute solutions Base Dissociation Constant Kb = [NH4+] x [OH- ] [NH3]
  • 67. Concentration and Strength The words concentrated and dilute indicate how much of an acid or base is dissolved in solution. • Number of moles of the acid or base in a given volume The words strong and weak refer to the extent of ionization or dissociation of an acid or base • How many of the particles ionize or dissociate into ions A sample of HCl added to a large volume of water becomes more dilute, but it is still a strong acid. Vinegar is a dilute solution of a weak acid.
  • 69. Acid-Base Reactions If you mix a solution of a strong acid containing hydronium ions with a solution of a strong base that has an equal number of hydroxide ions, a neutral solution results. • Final solution has properties that are characteristic of neither an acidic nor a basic solution. HCl(aq) + NaOH(aq) NaCl(aq) + H2O(l) H2SO4(aq) + 2KOH(aq) K2SO4(aq) + H2O(l)
  • 70. Neutralization Reactions Reactions of weak acids and weak bases do not usually produce a neutral solution. In general, reactions with which an acid and a base react in an aqueous solution to produce a salt and water are called neutralization reactions. reactions
  • 71. Making Salts Prepare potassium chloride by mixing equal molar quantities of hydrochloric acid and potassium hydroxide. HCl + KOH KCl + H20 Heating the solution to evaporate the water will leave the salt potassium chloride. In general, the reaction of an acid with a base produced water and salt
  • 72. Titration The number of moles of hydrogen ions provided by the acid are equivalent to the number of hydroxide ions provided by the base. HCl(aq) + NaOH(aq) NaCl (aq) + H20 (l) 1 mole 1 mole 1 mole 1 mole H2SO4(aq) + 2NaOH(aq) Na2SO4(aq) + 2H20 (l) 1 mole 2 mole 1 mole 2 mole When and acid & base are mixed, the Equivalence point is when the number of moles of hydrogen ions equals the number of moles of hydroxide ions.
  • 73. Sample Problem How many moles of sulfuric acid are required to neutralize 0.50 mol of sodium hydroxide? H2SO4(aq) + 2NaOH(aq) Na2SO4(aq) + 2H20 (l) • Mole ratio of H2SO4 to NaOH is 1:2 0.50 mol NaOH 1 mol H2SO4 = 0.25 mol H2SO4 2 mol NaOH
  • 74. Practice Problem How many moles of potassium hydroxide are needed to completely neutralize 1.56 mol of phosphoric acid? H3PO4(aq) + 3KOH(aq) K3PO4(aq) + 3H2O(l) 1.56 mol H3PO4 3 mol KOH = 4.68 mol H3PO4 1 mol H3PO4
  • 75. Titration You can determine the concentration of acid or base in a solution by performing a neutralization reaction. You must use an appropriate acid-base indicator to show when neutralization has occurred. In the lab, typically phenolphthalein for acid base neutralization reactions. Solutions that contain phenolphthalein turn from colorless to deep pink as the pH of the solution changes from acidic to basic.
  • 76. Titration a. Measured volume of an acid solution of unknown concentration is added to a flask
  • 77. Titration b. Several drops of the indicator are added to the solution while the flask is swirled
  • 78. Titration c. Measured volumes of the base of known concentration are mixed into the acid until the indicator just barely changes color.
  • 79. Titration Titration – the process of adding a known amount of solution of known concentration to determine the concentration of another solution. Standard solution – the solution of known concentration End point – the point at which the indicator changes color You can also use titration to find the concentration of a base using a standard acid.
  • 80. Titration Titration – the process of adding a known amount of solution of known concentration to determine the concentration of another solution. Standard solution – the solution of known concentration End point – the point at which the indicator changes color. The point of neutralization Equivalence point – the point in a titration where the number of moles of hydrogen ions = number of moles of hydroxide ions..
  • 81. Sample Problem A 25ml solution of H2SO4 is completely neutralized by 18ml of 1.0M NaOH. What is the concentration of the H2SO4 solution? H2SO4(aq) + 2NaOH(aq) Na2SO4(aq) + 2H20 (l) 0.018 L NaOH 1.0 mol NaOH 1 mol H2SO4 = 1L NaOH 2 mol NaOH 0.025L 0.36M H2SO4
  • 82. Practice Problem How many milliliters of 0.45M HCl will neutralize 25.0ml of 1.00M KOH? HCl + KOH H2O + KCl 0.025 L KOH 1.0 mol KOH 1 mol HCl 1L KOH 1 mol KOH 1 L HCl 1000 ml HCl = 56 ml HCl 0.45 mol HCl 1 L HCl
  • 83. Practice Problem What is the molarity of H3PO4 if 15.0 ml is completely neutralized by 38.5 ml of 0.150 M? H3PO4 + 3NaOH 3H2O + Na3PO4 0.0385 L NaOH 0.150 mol NaOH 1 mol H3PO4 1L NaOH 3 mol NaOH = 0.129M H3PO4 0.015L H3PO4
  • 85. Salt Hydrolysis A salt consists of an anion from an acid and a cation from a base. The salt forms as a result of a neutralization reaction Although solutions of many salts are neutral, some are acidic and others are basic. ..
  • 86. Salt Hydrolysis Salt Hydrolysis – the cations or anions of a dissociated salt remove hydrogen ions from or donate hydrogen ion to water. Hydrolyzing salts are usually derived from a strong acid and weak base or from a weak acid and a strong base. In general, salts that produce acidic solutions contain positive ions that release protons to water. Salts that produce basic solutions contain negative ions that attract protons from water.
  • 87. Salt Hydrolysis CH3COONa (aq) CH3COO- (aq) + Na+ (aq) Sodium ethanoate ethanoate ion sodium ion CH3COONa is the salt from a weak acid CH3COOH and a strong base NaOH In solution the salt is completely ionized.
  • 88. Salt Hydrolysis Salt Hydrolysis – the cations or anions of a dissociated salt remove hydrogen ions from or donate hydrogen ion to water. CH3COO-(aq) + H2O(l) CH3COOH (aq) + OH- (aq) BL base BL acid makes hydrogen-ion hydrogen-ion solution acceptor donor basic This process is called hydrolysis because it splits a hydrogen ion off a water molecule. Resulting solution contains a hydroxide-ion concentration greater than the hydrogen-ion concentration. Thus the solution is basic
  • 89. Salt Hydrolysis NH4Cl (aq) NH4+ (aq) + Cl- (aq) Ammonium Ammonium ion Chloride ion chloride NH4Cl is the salt from a strong acid (hydrochloric acid, HCl) and a weak base (ammonia, NH3) In solution the salt is completely ionized.
  • 90. Salt Hydrolysis NH4+(aq) + H2O(l) NH3(aq) + H3O+(aq) BL acid BL base makes hydrogen-ion hydrogen-ion solution donor acceptor acidic This process is also called hydrolysis because it splits a hydrogen ion off a water molecule. Resulting solution contains a hydrogen-ion concentration greater than the hydroxide-ion concentration. Thus the solution is acidic
  • 91. Salt Hydrolysis Equivalence Point Strong Acid pH= 7 neutral Strong Base Weak Acid pH > 7 basic Strong Base Strong Acid pH < 7 acidic Weak Base Equivalence point – the point in a titration where the number of moles of hydrogen ions = number of moles of hydroxide ions
  • 92. Buffers Buffer – a solution in which the pH remains relatively constant when small amounts of acid or base are added. A buffer is a solution of a weak acid and one of its salts, or a solution of a weak base and one of its salts. A buffer solution is better able to resist drastic changes in pH than is pure water.
  • 93. Buffers A solution of ethanoic acid (CH3COOH) and sodium ethanoate (CH3COONa) is an example of a typical buffer. CH3COOH and CH3COO- (source is the completely ionized CH3COONa) act as reservoirs of neutralizing power.
  • 94. Buffers CH3COO-(aq) + H+(aq) CH3COOH (aq) ethanoate ion hydrogen ion ethanoic acid When an acid is added to the solution, the ethanoate ions act as a hydrogen-ion sponge. CH3COOH (aq) + OH-(aq) CH3COO-(aq) + H2O (l) Ethanoic acid hydroxide ion ethanoate ion water When a base is added to the solution, the ethanoic acid and the hydroxide ions react to produce water and the ethanoate ion.
  • 95. Buffers The ethanoate ion is not strong enough base to accept hydrogen ions from water extensively. The buffer solution cannot control the pH when too much acid is added, because no more ethanoate ions are present to accept hydrogen ions. Buffer also become ineffective when too much base is added. No more ethanoic acid molecules are present to donate hydrogen ions.
  • 96. Buffers When too much acid or base is added, the buffer capacity is exceeded. Buffer capacity – the amount of acid or base than can be added to a buffer solution before a significant change in pH occurs.
  • 97. Buffers When a base is added to a buffered solution, the acidic form removes hydroxide ions from the solution. When an acid is added to a buffered solution, the basic form removes hydrogen ions from the solution.
  • 98. Buffers & Your Blood Your body function properly only when the pH of your blood lies between 7.35 and 7.45. Your blood contains buffers (hydrogen carbonate ions and carbonic acid) HCO3- (aq) + H+ (aq) H2CO3 (aq) hydrogen hydrogen ions carbonic acid carbonate ion As long as there are hydrogen carbonate ions available, the excess hydrogen ions are removed, and the pH of the blood changes very little.
  • 99. End of Section Chapter 19