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IB CHEMISTRY

Topic 8 Acids and bases

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Higher level
8.1 Theories of acids and bases
OBJECTIVES

• A Brønsted–Lowry acid is a proton/H+ donor and a Brønsted–


Lowry base is a proton/H+ acceptor.
• Amphiprotic species can act as both Brønsted–Lowry acids and
bases.
• A pair of species differing by a single proton is called a conjugate
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acid-base pair.
• Deduction of the Brønsted–Lowry acid and base in a chemical
reaction.
• Deduction of the conjugate acid or conjugate base in a chemical
reaction.
NOS: Acid-Base Hypothesis
• Greeks classifying substances based on taste –
sweet, salty, sour....
• Alkalis were known to neutralize the sour taste
• 1777 Antoine Lavoiser burnt phosphorus and
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sulfur with oxygen. These compounds were acidic
when dissolved in water. Therefore acids contain
oxygen. Created the word oxygen: Oxys = sour,
genes = born in Greek.
• 1809 Humphry Davy questioned this as HCl, H2S,
H2Te were acidic with no oxygen.
Key – Best hypothesis is the one with
the most predictive power
• Arrhenius proposed that salts form ions in
solution even without an electric current. Hence
acids were possibly substances that released H+
ions, and bases released OH- ions. But this did not
explain outside of aqueous solutions or for bases
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that did not have an –OH group.
• Bronsted and Lowry – acid is a H+ donor, base is a
H+ acceptor. NH3 can now be explained as a base.
• Lewis using his dot structures defined acids as an
electron pair acceptor, and a base as an electron
pair donor. BF3 + NH3 can now be explained.
Learning check - match
• Phosphorus and sulfur
• Lewis
oxides make acids
• HCl does not contain
oxygen • Lavosier
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• Acids give off H+ ions
• Acid is a H+ donor, base is • Davy
a H+ acceptor
• Acids are electron pair • Bronsted and Lowry
acceptors and and bases
are electron pair donors • Arrhenius
1 of 3. Arrhenius Acids and Bases

Arrhenius Acid – produce H+ ions (or


hydronium ions H3O+) eg. HCl

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Arrhenius Base – produce OH- ions eg. NaOH

(Problem: some bases don’t have hydroxide ions!)


2 of 3. Bronsted-Lowry Acids and
Bases
Bonsted-Lowry Acid – proton donor eg. H2O

Bronsted-Lowry Base – proton acceptor eg. NH3


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A “proton” is really just a hydrogen atom that has lost
it’s electron!
A Brønsted-Lowry acid is a proton donor
A Brønsted-Lowry base is a proton acceptor

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Base – conjugate acid pair
conjugate conjugate
base acid
acid base
Acid – conjugate base pair
The Brønsted definition means
NH3 is a BASE in water — and
water is itself an ACID
NH3 + H 2O NH4+ + OH -
Base Acid Acid Base
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Conjugate Pairs

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Amphoteric – can act as either an acid or a base
eg. Al2O3 as a base: Al2O3 + 6 HCl —> 2 AlCl3 + 3 H2O
Al2O3 as an acid: Al2O3 + 2NaOH + 3 H2O —> NaAl(OH)4

Amphiprotic – a type of amphoteric substance that


specifically can act as either an acid or base by accepting
or donating hydrogen ions
eg. water, diprotic acids

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Learning Check!
Label the acid, base, conjugate acid, and
conjugate base in each reaction:

HCl + OH -  Cl- + H O
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2

H2O + H2SO4  HSO4- + H3O+


8.2 Properties of acids and bases
OBJECTIVES

• Most acids have observable characteristic chemical reactions


with reactive metals, metal oxides, metal hydroxides, hydrogen
carbonates and carbonates.
• Salt and water are produced in exothermic neutralization
reactions.
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• Balancing chemical equations for the reaction of acids.
• Identification of the acid and base needed to make different
salts.
• Candidates should have experience of acid-base titrations with
different indicators.
Properties of Acids
• Often produce H+ in water (also written as the
hydronium ion H3O+ which is a hydrogen ion attached
to a water molecule)
• Taste sour
• Corrode metals
• Electrolytes
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React with bases (metal hydroxides) to form a salt,
water
• React with carbonates to form salt, water, CO2
• React with metals/metal oxides to form salt, H2
• pH is less than 7
• Turns blue litmus paper red, phenolphthalein
colourless, methyl orange red
Key reactions
1. Acid + base  salt + water

Eg. HCl + NaOH  NaCl + H2O


*Base can be a metal hydroxide, or a metal oxide.

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2. Acid + metal  salt + hydrogen

Eg. HCl + Mg  MgCl2 + H2 (unbalanced)

3. Acid + metal carbonate  salt + water + carbon dioxide

Eg. HCl + Na2CO3  NaCl + H2O + CO2 (unbalanced)


Acid Nomenclature Flowchart
ACIDS
start with 'H'

2 elements 3 elements

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hydro- prefix no hydro- prefix
-ic ending

-ate ending -ite ending


becomes becomes
-ic ending -ous ending
Learning check – nomenclature:

• HBr (aq)  hydrobromic acid

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• H CO  carbonic acid
2 3

• H2SO3  sulfurous acid


Properties of Bases
• Often produce OH- ions in water
• Taste bitter
• Are electrolytes
• Feel soapy, slippery
• React with acids to form salts and water
• pH greater than 7
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• Turns red litmus paper blue, phenolphthalein pink,
methyl orange yellow
• An alkali is a base that dissolves in water
8.3 The pH scale
OBJECTIVES

• pH = − log[H+(aq)] and [H+] = 10−pH.


• A change of one pH unit represents a 10-fold change in the
hydrogen ion concentration [H+].
• pH values distinguish between acidic, neutral and alkaline
solutions.
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• The ionic product constant, Kw = [H+] [OH-] = 10−14 at 298 K.
• Solving problems involving pH, [H+] and [OH-].
• Students should be familiar with the use of a pH meter and
universal indicator.
The pH scale is a way of expressing
the strength of acids and bases.
Instead of using very small numbers,
we just use the NEGATIVE power of
10 on the Molarity of the H+ (or OH-)
ion.

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pH 1 is 10 times stronger than pH 2
pH 1 is 100 times stronger than pH 3
etc…

Under 7 = acid
7 = neutral
Over 7 = base
Calculating pH
pH = - log10 [H+(aq)]

where [H+] is the concentration of hydrogen ions in mol dm-3

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Working backwards:

[H+ (aq)] = antilog (-pH)

Or

[H+] = 10-pH
Ionic product constant of water - Kw
Water undergoes very slight ionisation ... H2O(l) H+(aq) + OH¯(aq)

[H+(aq)] [OH¯(aq)]
Applying the equilibrium law: Kc
[H2O(l)]

As the dissociation is small, the water concentration is very large compared


with the dissociated ions and any changes to its value are insignificant; its
concentration can be regarded as constant.
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This “constant” is combined with (Kc) to get a new constant (Kw). At 25°C:

Kw = [H+(aq)] [OH¯(aq)] mol2 dm-6 = 1 x 10-14 mol2 dm-6

Because the constant is based on an equilibrium, Kw VARIES WITH


TEMPERATURE

Also note: pKw = 14 = pH + pOH


Kw variation
with
temperature
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• Kw gets larger as the temperature increases
• this means the concentration of H+ and OH¯ ions gets greater
• this means the equilibrium has moved to the right
• if the concentration of H+ increases then the pH decreases
• pH decreases as the temperature increases

Because the equation moves to the right as the temperature goes up, it must be an
ENDOTHERMIC process
Problem 1:
Calculate the pH of 0.02M HCl?
HCl  H+ + Cl¯
[H+] = 0.02M = 2x10-2 mol dm-3
pH = - log [H+] = 1.7
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Problem 2:
Calculate the pH of 0.1M NaOH?
NaOH  Na+ + OH¯
[OH¯] = 0.1M = 1x 10-1 mol dm-3

Method1:
Kw = [H+][OH¯] = 1 x 10-14 mol2dm-6
[H+] = Kw / [OH¯] = 1 x 10-13 moldm-3
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pH = - log[H+] = 13

Method 2:
pOH = 1
pOH + pH = 14
1 + pH = 14
pH = 13
8.4 Strong and weak acids and bases
OBJECTIVES

• Strong and weak acids and bases differ in the extent of


ionization.
• Strong acids and bases of equal concentrations have higher
conductivities than weak acids and bases.
• A strong acid is a good proton donor and has a weak conjugate
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base.
• A strong base is a good proton acceptor and has a weak
conjugate acid.
• Distinction between strong and weak acids and bases in terms
of the rates of their reactions with metals, metal oxides, metal
hydroxides, metal hydrogen carbonates and metal carbonates and
their electrical conductivities for solutions of equal
concentrations.
In a nutshell:
A strong acid or base is one that completely
dissociates in water.
Eg. HCl  H+ + Cl-
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<1% >99%
Strong acids/bases
Strong acids completely dissociate (split up) into ions in
aqueous solution

Eg. HCl  H+(aq) + Cl¯(aq) MONOPROTIC


HNO3  H+(aq) + NO3¯(aq)
H2SO4  2H+(aq) + SO42-(aq) DIPROTIC
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Strong bases completely dissociate into ions in aqueous
solution

Eg. NaOH  Na+(aq) + OH¯(aq)

 Note the arrow indicates COMPLETE DISSOCIATION


Weak acids/bases
Weak acids partially dissociate into ions in aqueous solution
Eg. ethanoic acid CH3COOH(aq) CH3COO¯(aq) + H+(aq)

Can also be written as:


HA(aq) + H2O(l) A¯(aq) + H3O+(aq)
or HA(aq) A¯(aq) + H+(aq)
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Weak bases partially dissociate into ions in aqueous solution

Eg. NH3(aq) + H2O(l) NH4+(aq) + OH¯(aq)

Note the arrow indicates PARTIAL DISSOCIATION


Determining weak/strong, acids/bases
experimentally
• A weak acid has a higher pH than a strong acid
of equal concentration
• A weak acid does not conduct electricity as
well as a strong acid
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• A weak acid reacts more slowly than a strong
acid eg. acid + metal  H2
Examples to be learnt - weak/strong,
acids/bases
Strong acids: hydrochloric acid, nitric acid,
sulfuric acid
Weak acids: carboxylic acids (eg. ethanoic acid is
vinegar), carbonic acid
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Strong bases: group 1 hydroxides (eg. NaOH),
barium hydroxide
Weak bases: ammonia and amines
Learning check:
Weak or strong, acid or base?

Ammonia NH4+ Weak base

Hydrochloric acid HCl Strong acid


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Potassium hydroxide KOH Strong base

Ethanoic acid CH3COOH Weak base


8.5 Acid deposition
OBJECTIVES

• Rain is naturally acidic because of dissolved CO2 and has a pH of


5.6. Acid deposition has a lower pH, usually below 5.0.
• Acid deposition is formed when nitrogen or sulfur oxides
dissolve in water to form HNO3, HNO2, H2SO4 and H2SO3.
• Sources of the oxides of sulfur and nitrogen and the effects of
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acid deposition should be covered.
• Balancing the equations that describe the combustion of sulfur
and nitrogen to their oxides and the subsequent formation of
HNO3, HNO2, H2SO4 and H2SO3.
• Distinction between the pre-combustion and post-combustion
methods of reducing sulfur oxides emissions.
• Deduction of acid deposition equations for acid deposition with
reactive metals and carbonates.
Acid deposition
Carbonic acid from CO2 in the atmosphere makes
rain a little acidic naturally:

CO2(g) + H2O(l) H2CO3(aq)

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2CO 3(aq) H+(aq) + HCO -(aq)
3

HCO3-(aq) H+(aq) + CO32-(aq)

Precipitation that is below pH 5.6 is considered


acid deposition.
Acid deposition – nitrogen
At high temperatures such as in engines:
N2(g) + O2(g)  2NO(g) (primary reaction)

This further reacts with oxygen:


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2NO(g) + O2(g)  2NO2(g)

This then reacts with water:


2NO2(g) + H2O(l)  HNO3(aq) + HNO2(aq)
Acid deposition – sulphur
Sulphur dioxide is released by burning coal (up to 3%
sulphur):
S(s) + O2(g)  SO2(g) (primary reaction)

This reacts with water to form sulfurous acid:


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SO2(g) + H2O(l) H2SO3(aq)

This can also react further with air, then water to form
sulphuric acid:

2SO2(g) + O2(g) 2SO3(g)


SO3(g) + H2O(l)  H2SO4(aq)
Prevention of acid deposition
Pre-combustion methods involve crushing and
washing coal with water to remove up to 90% of
solid sulphur.
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Post-combustion methods such as calcium oxide
(lime) can remove gaseous sulphur (and other
pollutants):

CaO(s) + SO2(g)  CaSO3(s)

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