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Title: HSC CHEMISTRY CORE TOPIC 2


1
HSC CHEMISTRY CORE TOPIC 2
  • THE ACIDIC ENVIRONMENT

2
INDICATORS
LE CHATELIERS PRINCIPLE
TITRATION
pH
VOLUMETRIC ANALYSIS
NEUTRALISATION
CHEMICAL EQUILIBRIUM
THE ACIDIC ENVIRONMENT
HISTORY Lavoisier Davy Arrhenius
CARBOXYLIC ACIDS
ACIDIC OXIDES
BRONSTED LOWRY THEORY
ESTERIFICATION
ACID RAIN
3
Subsection 1 Indicators were identified with the
observation that the colour of some flowers
depends on soil composition
4
Indicators
  • substances that have distinctive colours in
    different types of chemical environments
  • natural acid-base indicators are vegetable dyes
    that provide the colour of flowers and vegetables
  • LITMUS is a pink mixture of compounds extracted
    from lichens grown mainly in the Netherlands
  • today many indicators used are manufactured dyes

5
INDICATORS
INDICATOR pH RANGE COLOUR RANGE (low pH high pH)
Methyl orange 3.1 4.4 red (orange) yellow
Bromothymol blue 6.0 7.6 yellow (green) blue
Phenolphthalein 8.2 10.0 colourless - crimson
Litmus 5.5 8.0 red - blue
6
INDICATORS
7
INDICATORS
  • Universal Indicator is a mixture of
  • thymol blue
  • methyl red
  • bromothymol blue
  • phenolphthalein
  • dissolved in methanol, propan-1-ol and water

8
INDICATORS
  • A solution gives the following colours in each
    indicator. Deduce the approximate pH
  • Indicator Colour
  • methyl orange yellow
  • bromothymol blue yellow
  • phenolphthalein colourless

gt4.4 lt6.0 lt8.0
pH of solution is 4.4 6.0
9
INDICATORS
  • A solution gives the following colours in each
    indicator. Deduce the approximate pH
  • Indicator Colour
  • bromothymol blue blue
  • thymolphthalein colourless
  • phenol red red

gt 7.6 lt 9.5 gt 8.4
pH of solution is 8.4 9.5
10
INDICATORS
  • USES
  • Universal indicator used to test soil
    acidity/alkalinity (pH)
  • plants have preference for alkaline/neutral/acid
    soils choice of crop
  • diseases that affect plants thrive in soils with
    a particular pH range
  • pH affects availability of nutrients
  • Phenol red used to test acidity/alkalinity of a
    swimming pool level of disinfection

11
Clay Minerals in Soil
Metal ions bind to negative surface
H are able to displace the surface cations from
the clay. If aluminium ions are displaced by H
the soil becomes toxic to crops growing in the
soil.
12
  • Subsection 2
  • While we usually think of the air around us as
    neutral, the atmosphere naturally contains acidic
    oxides of carbon, nitrogen and sulfur. The
    concentrations of these acidic oxides have been
    increasing since the Industrial Revolution

13
Oxides of Period 3
  • NaOH(s) ?
  • MgO(s) H2O(aq) g
  • S(s) O2(g) g
  • SO2(g) H2O(aq) g
  • P4(s) O2(g) g P2O5(s)
  • P2O5(s) H2O(aq) g

14
Oxides of Period 3
  • NaOH(s) g Na(aq) OH-(aq)
  • MgO H2O g Mg(OH)2
  • S O2 g SO2
  • SO2 H2O g H2SO3 (sulfurous acid)
  • 2H2SO3 O2 g 2H2SO4 (sulfuric acid)
  • P4 5O2 g 2P2O5
  • P2O5 3H2O g 2H3PO4 (phosphoric acid)
  • Cl2O7 H2O g 2HClO4 (perchloric acid)

15
Oxides of Period 3
Oxide/ Hydroxide Na2O (NaOH) MgO Al2O3 SiO2 P2O5 SO2 Cl2O7
Bonding
Acid/base property amphoteric acidic
16
Acid/Base Properties of Oxides
  • BASIC OXIDES
  • metal oxides and hydroxides (ionic compounds)
  • soluble oxides react with water to form
    alkaline/basic solutions
  • Na2O(s) H2O(l) ? 2NaOH(aq)
  • react with acids/acidic oxides to form salts
  • CuO(s) H2SO4(aq) ? CuSO4(aq) H2O(l)
  • CaO(s) SO2(g) ? CaSO3(s)

17
Acid/Base Properties of Oxides
  • ACIDIC OXIDES
  • generally oxides of non-metals (covalent
    compounds
  • called acid anhydrides
  • react with water to produce an acidic solution
  • CO2(g) H2O(l) ? H2CO3(aq)
  • react with bases to form salts
  • CO2(g) CaO(s) ? CaCO3(s)
  • 2NaOH(l) SiO2(s) ? Na2SiO3(s) H2O(l)

18
Acid/Base Properties of Oxides
  • AMPHOTERIC OXIDES
  • react with acids and bases
  • Al2O3, BeO, ZnO, PbO, SnO
  • Al2O3(s) 6HCl(aq) g 2AlCl3(aq) 3H2O(l)
  • Al2O3(s) 2NaOH(aq) g2NaAlO2(aq) H2O(l)
  • NEUTRAL OXIDES
  • do not react with acids or bases
  • CO, N2O, NO

19
Group A Oxides
20
Salts
  • in general acids and bases form salts
  • the type of salt is determined by the acid
  • HCl ? chloride salts
  • HNO3 ? nitrate salts
  • H2SO4 ? sulfate salts
  • H3PO4 ? phosphate salts

21
A Saturated Solution of NaCl
Dissolution NaCl(s)g Na(aq) Cl-(aq)
NaCl
System at 25oC
22
A Saturated Solution of NaCl
Radioactive 24NaCl is introduced into the beaker
23
A Saturated Solution of NaCl
CHEMICAL EQUILIBRIUM
Dissolution NaCl(s) g Na(aq)
Cl_(aq) Recrystallisation NaCl(s) f Na(aq)
Cl_(aq)
24
Chemical Equilibrium
25
CHEMICAL EQUILIBRIUM
  • only occurs in a closed system
  • no interchange of matter between system and
    surroundings
  • occurs in physical and chemical systems
  • temperature of the system remains constant
  • the rate of the forward reaction equals the rate
    of the reverse reaction
  • refers to reversible reactions where the forward
    reaction occurs simultaneously with reverse
    reaction

26
CHEMICAL EQUILIBRIUM
27
Le CHATELIERS PRINCIPLE
  • French chemist Henri Le Chatelier (1850-1936)
    studied changes in systems that were in a state
    of equilibrium
  • If a stress is applied to a system in a state of
    chemical equilibrium, the system changes to
    relieve the stress
  • may be changes in
  • concentration
  • volume and pressure
  • temperature

28
CONCENTRATION
  • increasing the concentration of a reactant or
    product will cause the system to favour the
    direction which will decrease the concentration
    of that substance
  • decreasing the concentration of a reactant or
    product means the rate of the reaction using up
    that substance will decrease in rate
  • the rate of the other reaction to produce that
    substance will now have the faster rate

29
CONCENTRATION
  • equilibria with solids and pure liquids
  • e.g. C(s) H2O(g) n CO(g)
    H2(g)

30
PRESSURE
  • changes in pressure have little effect on solids
    and liquids as they are only very slightly
    compressible
  • changes in pressure have significant effects on
    the concentration of GASES
  • gas pressure is proportional to the number of
    molecules
  • changing the partial pressure of a gas changes
    its concentration

31
Partial Pressure of a Gas
32
PRESSURE
  • Adding an inert gas
  • does not change the partial pressures of any of
    the other gases
  • no effect on equilibrium

33
VOLUME CHANGES
  • reducing the volume of the gas by half doubles
    the pressure of the gas

34
VOLUME CHANGES
  • decreasing volume - reaction rate increases in
    the direction that produces the smaller number of
    molecules

e.g. 2SO2(g) O2(g) n 2SO3(g)
  • in the reaction above there will be a shift to
    the
  • right as the forward reaction increases in
    rate to
  • minimise the pressure changes
  • producing less molecules reduces the pressure
  • increasing the volume decreases the pressure
  • causes a shift to the left in the above reaction
    as this produces the larger number of molecules

35
CHEMICAL EQUILIBRIUM
2NO2 n N2O4
  • analyse the changes made to the equilibrium
    system shown in the diagram at the left

36
TEMPERATURE
  • increasing the temperature increases the reaction
    rate
  • this is due to an increase in the fraction of
    collisions in which the total kinetic energy of
    reacting particles is at least equal to the
    activation energy
  • increasing the temperature favours the
    endothermic reaction
  • decreasing the temperature favours the exothermic
    reaction

37
TEMPERATURE
38
Mass-Gas Volume
  1. Calculate the mass of 18.25L of ammonia gas at
    25.0oC and 100.0kPa.
  2. At 100.0 kPa and 25.0oC, how many litres of
    carbon dioxide gas will be produced when 75.0g of
    calcium carbonate is decomposed into calcium
    oxide?

39
Mass-Gas Volume
  • Solid lithium hydroxide has been used in space
    craft to remove carbon dioxide from air. Lithium
    carbonate and water are formed.
  • What mass of lithium hydroxide would be
    needed to remove 250.0 L of carbon dioxide at
    100.0 kPa and 25.0oC?

40
Acid Rain
  • Sulfur dioxide
  • natural and man-made sources
  • reactions to produce it
  • sulfur compounds in coal S(s) O2(g) ? SO2(g)
  • smelting of sulfide ores ZnS(s) O2(g) ? Zn(s)
    SO2(g)
  • oxidation of H2S decay and industrial
  • 2H2S 3O2(g) ? 2H2O(l) 2SO2(g)
  • reactions to produce acidic solutions
  • effects
  • living things and environment
  • corrosion metals, limestone buildings (CaCO3)

41
Acid Rain
  • Nitrogen oxides NOx (NO, NO2)
  • natural and man-made sources
  • reactions to produce it
  • high temperature engines
  • N2 O2 g 2NO (neutral oxide)
  • 2NO O2 g 2NO2 (acidic oxide)
  • reactions to produce acidic solutions
  • 2NO2 H2O g HNO2 HNO3
  • effects
  • living things and environment

42
Production of Ozone
photodecomposition NO2 g NO O ozone formation O
O2 g O3
regeneration of nitrogen dioxide O3 NO g O2
NO2
Ozone is a secondary pollutant in the troposphere
43
Photochemical Smog
44
What is acid rain?
More appropriate term is acidic
deposition -snow, fog, sleet, haze, dry
deposition
What is Acid Rain? Pure water pH 7 Natural rain
pH 5-6 Acid rain pH lt 5
45
Acid Rain
  • 1730s originated at height of Industrial
    Revolution
  • 1872 Robert Smith, an English chemist, coined
    the phrase acid rain
  • 1950s lake acidification first described
  • 1960s became more noticeable and subsequently
    became worse in rural areas
  • ? tall chimneys on factories allow wind to
    transport pollutants far away from sources of
    production

46
(No Transcript)
47
Acid Rain
 Out west, in the Rocky Mountains scientists are
finding that power plant emissions are saturating
high-elevation watersheds in Colorado with
acid-causing nitrogen. Evergreen forests are
losing their needles and tree health is declining
throughout the forest range
48
Acid Rain
Acid rain damage Blue Ridge Mountains North
Carolina
49
Acid Rain
Acid rain damage on monument CaCO3 (s) H2SO4
(aq) ? CaSO4 (aq) CO2 (g) H2O (l)
50
Acid Rain
Tasmania - Queenstown emerged as a boomtown of
the 1890s when gold and minerals were discovered
at Mount Lyell. The strange but arresting
'moonscape' that surrounds the town was caused by
acid-rain during the mining era.
51
Acid Rain
  • 1984 reported almost half of Germanys Black
    Forest damaged by acid rain
  • Other areas
  • - acidification of lakes in Scandinavia
  • - Taj Mahal and many statues in Europe increased
    deterioration due to acid rain
  • - substantial problem in Europe, China and
    Russia as burn higher S-containing coal to
    generate electricity
  • - aluminium

52
Acid Rain
  • Sulfur dioxide
  • natural and man-made sources
  • reactions to produce it
  • sulfur compounds in coal
  • smelting of sulfide ores
  • oxidation of H2S decay and industrial
  • reactions to produce acidic solutions
  • effects
  • living things and environment
  • corrosion metals, limestone buildings (CaCO3)

53
Acid Rain
54
SO2 Pollution
Killer smogs of London 1952, 1956, 1957, 1962
55
Acid Rain
56
Acid Rain
  • Nitrogen oxides NOx (NO, NO2)
  • natural and man-made sources
  • reactions to produce it
  • high temperature engines
  • N2 O2 g 2NO (neutral oxide)
  • 2NO O2 g 2NO2 (acidic oxide)
  • reactions to produce acidic solutions
  • 2NO2 H2O g HNO2 HNO3
  • effects
  • living things and environment

57
http//www.csiro.au/promos/ozadvances/series14acid
rainmovb.htm
58
Changes in Sulfate across the USA
http//nadp.sws.uiuc.edu/data/amaps/so4/amaps.html
59
  • NADP Annual Maps

60
Production of Ozone
photodecomposition NO2 g NO O ozone formation O
O2 g O3
O3 NO g O2 NO2
Ozone is a secondary pollutant in the troposphere
61
Photochemical Smog
62
Table 4.4 Text p. 124
63
Common Acids
Acetic acid
Phosphoric acid
Sulfuric acid
64
3. Acids occur in many foods, drinks and even
within our stomachs
  • Naturally occurring
  • acetic/ethanoic (vinegar)
  • citric/2-hydroxypropane-1,2,3-tricarboxylic acid
    (citrus fruit)
  • hydrochloric (stomach)

65
3. Acids occur in many foods, drinks and even
within our stomachs
66
Acids

Aspirin acetylsalicylic acid
67
Amino acids
68
Acids
  • Manufactured/Synthetic
  • sulfuric acid
  • car batteries, fertiliser (NH3)2SO4, detergents,
    catalyst production ethanol and esters
  • nitric acid
  • fertilisers , explosives

69
Bases
  • Naturally Occurring
  • ammonia NH3
  • also manufactured to produce fertilisers (Haber
    process)
  • metal oxides Fe2O3, CuO
  • carbonates CO32- (Na2CO3, CaCO3)
  • Manufactured/Synthetic
  • sodium hydroxide soap, Draino (NaOH)
  • calcium oxide, calcium hydroxide

70
Bases
71
Acids Bases
Text p. 131-133
72
Self-Ionisaton/Autolysis of H2O
  • in a sample of pure water a very small amount of
    the molecules react with each other
  • this is called the self-ionisation of water.
  • H2O(l) H2O(l) n H3O(aq) OH(aq)
  • at 25oC OH- H3O 1.0x10-7 mol/L
  • KW OH- x H3O 1.0 x 10-14
  • in any aqueous solution the OH- and H3O are
    interdependent but KW is constant
  • aqueous solutions are neutral, acidic, basic

73
Using Kw
  • If the hydroxide ion concentration of a sodium
  • hydroxide solution is 1.5 x 10-3mol/L at 25oC,
  • what is the hydrogen ion concentration?

74
Using Kw
  • At 25oC an aqueous solution has a hydrogen ion
    concentration of 2.4 x 10-3mol/L.
  • What is the hydroxide ion concentration in this
    solution?

75
The pH Scale
  • proposed in 1909 by Danish scientist Soren
    Sorensen
  • pH means power of the Hydrogen ion
  • pH -logH the negative logarithm of the
    hydrogen ion concentration
  • neutral, acidic, basic solutions
  • to obtain the H given the pH
  • H 10-pH

76
pH A measure of acidity
  • Nitric acid (HNO3) is used in the production of
    fertilizer, dyes, drugs, and explosives.
    Calculate the pH of a HNO3 solution having a
    hydrogen ion concentration of 0.76 M.
  • The pH of a brand of orange juice is 3.33.
    Calculate the H ion concentration.
  • The OH ion concentration of a blood sample is
    2.5 x 107 M. What is the pH of the blood?

77
pH
  • Show that a change in pH from 4.75 to 3.75
  • corresponds to a tenfold increase in hydrogen ion
  • concentration.

78
Problems with B-L Theory
  • The theory works very nicely in all protic
    solvents
  • but fails to explain acid-base behavior in
    aprotic
  • solvents and some non-solvent situations.
  • A more general concept of acids and bases was
  • proposed by G.N. Lewis at about the same
  • time Bronsted-Lowry theory was proposed.

79
4.2 Bronsted-Lowry theory
80
3.2.2 plan and perform a first-hand
investigation to measure the pH of identical
concentrations of strong and weak acids
81
Strong Acid
unionised acid molecule
hydrogen ion
Would the solution conduct (be an electrolyte)?
anion from acid
100 ionisation of HA
HA g H A-
82
Strong Acid
  • For example
  • HCl(aq) ? H(aq) Cl-(aq)
  • OR HCl(g) H2O(l) ? H3O(aq) Cl-(aq)
  • HNO3(aq) ? H(aq) NO3-(aq)
  • OR
  • HNO3(l) H2O(l) ? H3O(aq) NO3-(aq)

83
Weak Acid
At any one time, only a fraction of the molecules
are ionised
HA
H
A-
Would the solution be conductive?
Partial ionisation of HA
HA ? H A-
84
Weak Acid
  • Note the use of the double arrow
  • The unionised acid molecules are in EQUILIBRIUM
    with the ionised hydrogen ion and anion from the
    acid
  • CH3COOH(aq) n H(aq) CH3COO-(aq)
  • OR
  • CH3COOH(l) H2O(l) nH3O(aq) CH3COO-(aq)

HA ? H A-
85
Acids and Bases
  • STRONG ACIDS HCl, HBr, HI, H2SO4, HNO3, HClO3,
    HClO4
  • WEAK ACIDS organic acids, and H2SO3, HNO2,
    H3PO4, H2CO3
  • STRONG BASES ionise completely in water to
    produce OH- ions
  • LiOH, Na2O, KOH, Ba(OH)2 ALKALIS strong
    soluble bases
  • WEAK BASES NH3, CO32-, HCO3-

86
Acids and Bases
  • Weak bases like NH3 react with water to produce
    hydroxide ions
  • This also forms an EQUILIBRIUM
  • NH3(g) H2O(l) ? NH4(aq) OH-(aq)
  • ammonium

  • ion

87
Acids
  • If the degree of ionisation of a weak acid is
    known then the pH of the solution can be
    determined.
  • e.g. If a solution of 0.037M hydrofluoric acid,
    HF, is 12.9 ionised what is the pH of the
    solution? HF n H F-
  • H 12.9/100 x 0.037 M 0.00477 M
  • pH -log(0.00477) 2.32
  • Finish worksheet on p.100 in SSB

88
Acids and Bases
  • strength
  • weak limited ionisation forming an equilibrium
    system
  • strong complete (100) ionisation
  • concentration
  • dilute
  • concentrated

89
Dilution
water (solvent)
solute
moles of solute remain constant
diluted, Mfinal
Vfinal
molesinitial molesfinal
Vinitial
concentrated, Minitial
adding water lowers the solute concentration
Mfinal x Vfinal Minitial x Vinitial
90
Acid Concentration
  • dilute solution of a strong acid
  • low number of moles of acid molecules per L of
    solution
  • all acid molecules completely ionised
  • concentrated solution of weak acid
  • higher number of moles of acid molecules per L of
    solution
  • acid molecules only partially ionised

91
Monoprotic Acid
  • contains only one ionisable hydrogen
  • HCl, HNO3, CH3COOH

92
Diprotic Acid
  • contains 2 ionisable hydrogens
  • 2-step ionisation
  • First ionisation
  • H2SO4 ? H HSO4- (complete)
  • Second ionisation
  • HSO4- n H SO42- (partial)

93
Triprotic Acid
  • contains 3 ionisable hydrogens
  • phosphoric acid H3PO4
  • First ionisation
  • H3PO4 n H H2PO4- (partial)
  • Second ionisation
  • H2PO4- n H HPO42-
  • Third ionisation
  • HPO42- n H PO43-

94
Strong Acid
unionised acid molecule
hydrogen ion
anion from acid
95
Weak Acid
HA
H
A-
96
Gas-neutralisation Problems
  • At 25oC and 100 kPa, 2.5 litres of hydrogen
    chloride gas is bubbled through a sodium
    hydroxide solution. If the solution is 0.50M
    what volume would be needed to completely
    neutralise the gas?
  • balanced equation
  • moles of HCl
  • moles of sodium hydroxide needed
  • volume of solution

97
Gas-neutralisation Problems
  • 3.0 litres of carbon dioxide is bubbled through
    200.0 mL of 0.15 M calcium hydroxide solution at
    25oC and 100 kPa. What mass of calcium carbonate
    precipitate will form?
  • If 350.0 mL of a solution of potassium hydroxide
    completely neutralises 5.0 L of sulfur dioxide
    gas at 25oC and 100 kPa, what is the
    concentration of the solution?

98
Gas-neutralisation Problems
  • What volume of 0.25M barium hydroxide solution
    would completely neutralise 10.0 L of hydrogen
    chloride gas at 25oC and 100 kPa?
  • 500.0mL of hydrogen chloride gas at 25oC and
    100kPa is bubbled through 800.0mL of distilled
    water. Assuming all the hydrogen chloride
    reacts, what is the pH of the solution?

99
pH of Solutions
  1. 175.0mL of a 0.085M solution of sodium hydroxide
    is mixed with 150.0mL of a 0.15M solution of
    hydrochloric acid. Determine the pH of the final
    solution.
  2. 250.0mL of a 0.15M solution of potassium
    hydroxide is mixed with 275.0mL of a 0.085M
    solution of nitric acid. Determine the pH of the
    final solution.

100
pH of Solutions
  • 50.0mL of a 0.050M solution of barium hydroxide
    is mixed with 75.0mL of a 0.100M solution of
    hydrochloric acid. Determine the pH of the final
    solution.

101
pH Meter
  • tests the voltage of the electrolyte
  • converts the voltage to pH
  • very cheap, accurate
  • must be calibrated with buffer solutions
  • non-destructive testing does not change
    solution being tested

102
pH of Acid Solutions
3.3.2 plan and perform a first-hand investigation
to measure the pH of identical concentrations of
strong and weak acids
Acid Molarity pH (0.1) H
HCl 0.1 1.0 0.10
C6H8O7 0.1 1.5 0.032
CH3COOH 0.1 2.9 0.00013
103
Molecular Structure and Acid Strength
  • the strength of an acid depends on its tendency
    to ionize.
  • for general acids of the type HX
  • The stronger the bond, the weaker the acid.
  • The more polar the bond, the stronger the acid.
  • for the hydrohalic acids, bond strength plays the
    key role giving HF lt HCl lt HBr lt HI

104
Molecular Structure and Acid Strength
  • The electrostatic potential maps show all the
    hydrohalic acids are polar. The variation in
    polarity is less significant than the bond
    strength which decreases from 567 kJ/mol for HF
    to 299 kJ/mol for HI.

105
Acids
  • Write equations to show the 2-step ionisation in
    water of the weak sulfurous acid, H2SO3

106
Acids as Food Additives
  • acidulant gives a sharp/tart taste to food
  • antimicrobials lowers pH to inhibit growth of
    bacteria, yeasts or molds
  • antioxidants slows oxidation which causes
    spoilage e.g. fats and oils
  • inhibit/block enzymes that continue natural
    ripening after harvest causes browning

107
3.3.6 Identify data, gather and process
information from secondary sources to identify
examples of naturally occurring acids and bases
and their chemical composition
Name Formula pH in natural form Naturally found in
Acetic CH3COOH 3-5 Vinegar, grapes, wine
Ascorbic C6H8O6 2-3 Fruit (esp. citrus), vegetables
Carbonic H2CO3 2-3 Acid rain
Citric C6H8O7 2-3 Citrus fruits
Formic CHOOH 3-5 Poison of stinging ants/insects
Hydrochloric HCl 0.1-2 Gastric juice in stomach
Ammonia NH3 9-11 Volcanic gases, decomposed plant/animal matter
Caffeine C8H10N4O2 8-10 Coffee beans, cola nuts
Nicotine C8H14N2 8-10 Tobacco leaves
Limestone CaCO3 8-10 Limestone
108
Acids and Bases
  • OPERATIONAL
  • DEFINITION
  • based on observed properties
  • what do they do?

109
Acids
  • taste sour
  • change the colour of indicators e.g. blue litmus
    to red
  • neutralise bases and basic oxides
  • some are corrosive
  • react with active metals such as zinc, magnesium
    giving off hydrogen gas
  • aqueous solutions of acids conduct electricity
    they are ELECTROLYTES

110
Bases
  • taste bitter
  • change the colour of indicators e.g turn red
    litmus blue
  • neutralise acids and acidic oxides
  • some are corrosive
  • solutions of soluble bases in water are
    electrolytes

111
Acids and Bases
  • CONCEPTUAL
  • DEFINITIONS
  • a theoretical framework to explain observed
    properties
  • more likely to change as our knowledge increases

112
4.1 Outline the historical development of ideas
about acids
  • 1778 Antoine Lavoisier
  • oxides of P and S combined with water to produce
    acidic solutions
  • S O2 ? SO2 H2O ? H2SO3
  • oxygen is responsible for acidity
  • named oxygen from Greek oxys sharp/sour and
    genes born/form (acid former)

113
4.1 Outline the historical development of ideas
about acids
  • 1811 Sir Humphrey Davy
  • acids contain the element hydrogen - so hydrogen
    is responsible for acidity

114
4.1 Outline the historical development of ideas
about acids
  • 1887 Svante Arrhenius
  • acidic and basic solutions conduct
  • electricity so electrolytes (ions)
  • acids react with metals to produce
  • hydrogen so ions involved
  • developed ionic theory of electrolytes for which
    he received a Nobel Prize in 1903

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4.1 Outline the historical development of ideas
about acids
  • 1887 Svante Arrhenius
  • acids are substances that release H
  • in aqueous solution
  • e.g. HCl(aq) g H(aq) Cl-(aq)
  • H2SO4(aq) g 2H(aq) SO42-(aq)
  • bases are substances that release OH- ions in
    aqueous solution
  • e.g. NaOH(aq) g Na(aq) OH-(aq)
  • Ba(OH)2(aq) g Ba2(aq) 2OH-(aq)

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4.1 Outline the historical development of ideas
about acids
  • Neutralisation
  • HCl(aq) NaOH(aq) ? NaCl(aq) H2O(l)
  • H(aq) OH-(aq) ? H2O(l)

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Problems with Arrhenius Theory
  • the role of the solvent? is an acid an acid in
    any solvent
  • all salts should produce neutral solutions
    neither acidic nor basic
  • the need for hydroxide as the base
  • e.g. NH4OH as the base and not NH3

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The Hydrogen Ion
  • a proton with a 1 charge and extremely small
    mass/volume
  • high charge density and intense electric field
  • too reactive to exist independently in a very
    polar solvent like water
  • the hydronium ion, H3O

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Subsection 4 Because of the prevalence and
importance of acids, they have been used and
studied for hundreds of years. Over time, the
definitions of acid and base have been refined
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4.2 Outline the Bronsted-Lowry theory of acids
and bases
  • in 1923 a more general theory of acid-base
    behaviour was independently proposed by Danish
    chemist J Bronsted and English chemist T Lowry
  • Bronsted-Lowry theory defines
  • an acid as a species from which a proton can be
    removed (acids are proton donors)
  • a base as a species that can remove a proton from
    an acid (bases are proton acceptors)

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4.2 Bronsted-Lowry theory
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4.2 Bronsted-Lowry Theory
  • CH3COOH(l) H2O(l) nH3O(aq) CH3COO-(aq)
  • NH3(g) H2O(l) n NH4(aq) OH-(aq)
  • an acid-base reaction is one in which a proton is
    transferred from an acid to a base
  • a proton-transfer reaction

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4.2 Bronsted-Lowry theory
The role of the solvent Hydrogen chloride in
liquid ammonia
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4.2 Bronsted-Lowry theory
  • a broader definition which shows the
    complementary nature of acids and bases
  • shows the role of the solvent which can be a
    proton acceptor or proton donor
  • includes more species that Arrhenius Theory -
    molecules and ions
  • acid must contain hydrogen to have a proton
    removed

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4 Bronsted-Lowry theory
  • each B-L reaction involves two acid-base pairs
    called CONJUGATE PAIRS - two species that differ
    by a proton
  • conjugate means coupled or joined

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4 Bronsted-Lowry theory
conjugate acid
base
acid
conjugate base
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Acids and Bases
  1. What is the pH of a solution made by diluting
    2.50mL of 6.0M HCl to 500.0mL?
  2. What is the pH of a 0.035M solution of Ba(OH)2 ?
  3. The pH of a HCl solution is 1.25. If 200.0mL of
    this solution is diluted to 500.0mL, what is the
    pH of this new solution?

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4 AMPHIPROTIC SPECIES
  • Molecules or ions that can accept OR donate a
    proton
  • Act as acids or act as bases
  • e.g. H2O(l) H2O(l) n H3O(aq) OH(aq)

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4 AMPHIPROTIC SPECIES
  • hydrogen carbonate ion and a strong acid and base
  • HCO3-(aq) OH-(aq) ? CO32-(aq) H2O(l)
  • acid base
  • HCO3-(aq) H3O(aq) ? H2CO3(aq) H2O(l)
  • base acid
  • H2CO3(aq) D CO2(g) H2O(l)

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4 AMPHIPROTIC SPECIES
  • hydrogen carbonate ion and a weak acid/base
  • HCO3- H2O D CO32- H3O
  • acid base
  • HCO3- H2O D H2CO3 OH-
  • base acid

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4 AMPHIPROTIC SPECIES
  • The hydrogen sulfate ion is amphiprotic.
  • Write balanced equations to show this behaviour.
    (use H3O and OH-)
  • A solution of sodium hydrogen sulfate in water
    turns blue Litmus red. Use an equation to
    explain this behaviour.

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4.2.8 4.3.3 TITRATIONS
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Validity Reliability
  • TITRATION - VALIDITY
  • appropriate reaction acid and base
  • primary std or standardised secondary std
  • appropriate indicator for type of titration
  • accurate measuring instruments volumetric
    glassware volumetric pipette, burette
  • correct washing procedures and use e.g. method
    of operating the pipette and burette
  • RELIABILITY
  • 3 or more trials reproducible ?average titre

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4.2.4 Identify a range of salts which form
acidic, basic and neutral solutions and explain
their acidic, neutral or basic nature
0.1M Salt Solution pH Universal Indicator pH Probe
NaCl 6-7 6.5
NH4Cl 4-5 4.5
NaCH3COO 8-9 9.5
NaNO3 6-7 7.2
Na2CO3 10-11 9.9
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4.2.4 Identify a range of salts which form
acidic, basic and neutral solutions and explain
their acidic, neutral or basic nature
  • TEXT p. 154 TABLE 5.4
  • Summary of salts formed from different types of
    acids bases

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Indicators
  • Phenolphthalein is a commonly used indicator for
    titrations, and is a weak acid.
  • the weak acid is colourless and its ion is bright
    pink.
  • Adding extra hydrogen ions shifts the position of
    equilibrium to the left, and turns the indicator
    colourless.
  • Adding hydroxide ions removes the hydrogen ions
    from the equilibrium which shifts to the right to
    replace them - turning the indicator pink.

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Strong Acid with Strong Base
HCl NaOH g NaCl H2O
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Strong Acid with Strong Base
pH finishes high
8.3-10
Equivalence point pH 7
pH starts low
3.1-4.4
HCl NaOH g NaCl H2O
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Weak Acid with Strong Base
phenolphth
methyl orange
CH3COOH NaOH g NaCH3COO H2O
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Weak Acid with Strong Base
pH finishes high
Equivalence point
phenolphth
pH starts higher
methyl orange
CH3COOH NaOH g NaCH3COO H2O
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Weak Base with Strong Acid
phenolphth
methyl orange
NH3 HCl g NH4Cl H2O
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Weak Base with Strong Acid
pH starts moderately high
Equivalence point
phenolphth
methyl orange
pH finishes low
NH3 HCl g NH4Cl H2O
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Weak Acid with Weak Base
pH
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4.2.4 Identify a range of salts which form
acidic, basic and neutral solutions and explain
their acidic, neutral or basic nature
  • For each of the salts below,
  • give the formula
  • state the acid and base that produced the salt
  • state whether you would expect 0.1M aqueous
    solutions to be neutral, acidic or basic
  • explain why, giving appropriate equations where
    necessary
  • 1. barium nitrate 2. sodium methanoate
  • 3. sodium carbonate 4. ammonium nitrate
  • 5. sodium sulfite 6. potassium bromide

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4.2.7 Neutralisation
  • a proton transfer reaction
  • exothermic reaction
  • for example
  • HCl(aq) NaOH(aq) g NaCl(aq) H2O(aq)
  • DH -56.1 kJmol-1

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4.3.5 Neutralisation safety measure and
minimise damage in chemical spills
  • Factors to consider
  • type of acid or base weak or strong,
    concentrated or dilute
  • volume few mL on laboratory bench or much
    larger volume in more public place

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4.3.5 Neutralisation safety measure and
minimise damage in chemical spills
  • weak acids and bases are safer to use
  • neutralise acids
  • Na2CO3 solid, cheap, easy to use, excess does
    not present problems of disposal
  • neutralise acids and alkalis
  • NaHCO3 amphiprotic
  • HCO3- OH- ? CO32- H2O
  • HCO3- H ? H2CO3 ? CO2 H2O
  • Booklet p. 142-144

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Sources of H in the Body
Ketone bodies Acetone Betahydroxybutyric
acid Acetoacetate (CH3COCH2COOH)
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4.2.9 BUFFERS
  • A buffer is a solution that resists a change in
    its pH when acid (H3O) or base (OH-) is added to
    it.
  • based on chemical equilibrium
  • A solution of a weak acid and its conjugate base
    OR a weak base and its conjugate acid
  • nearly all biochemical reactions are influenced
    by the pH of their fluid environment
  • maintaining the pH of blood
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