Chapter 3
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Chapter 3
ACID AND BASES
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• Electrolyte - substance that, when dissolved in water, results in a solution that can conduct electricity.
• Nonelectrolyte - substance that, when dissolved, results in a solution that does not conduct electricity.
nonelectrolyte weak electrolyte strong electrolyte
ELECTROLYTIC PROPERTIES
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• Strong Electrolyte – 100% dissociation (breaking up of compound into cations and anions
NaCl (s) Na+ (aq) + Cl- (aq)H2O
• Weak Electrolyte – not completely dissociated
CH3COOH CH3COO- (aq) + H+ (aq)
A reversible reaction. The reaction can occur in both directions.
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Nonelectrolyte does not conduct electricity?
No cations (+) and anions (-) in solution
C6H12O6 (s) C6H12O6 (aq)H2O
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• Hydration - process in which an ion is surrounded by water molecules arranged in a specific manner.
- helps to stabilize ions and prevents cations from combining with anions.
H2O
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• Have a sour taste.
• Turn litmus paper from blue to red. • React with certain metals to produce hydrogen gas.
• React with carbonates and bicarbonates to produce carbon dioxide gas
2HCl (aq) + Mg (s) MgCl2 (aq) + H2 (g)
2HCl (aq) + CaCO3 (s) CaCl2 (aq) + CO2 (g) + H2O (l)
• Aqueous acid solutions conduct electricity.
PROPERTIES ACIDS
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• Have a bitter taste.
• Turn litmus paper from blue to red.• Feel slippery. Many soaps contain bases.
• Aqueous base solutions conduct electricity.
• Examples:
PROPERTIES OF BASES
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ROLE OF WATER TO SHOW PROPERTIES ROLE OF WATER TO SHOW PROPERTIES OF ACIDSOF ACIDS
Anhydrous pure acid does not show acidic properties
do not dissociate to form hydrogen ion (H+). When dissolved in water show the properties of acids. Why? - acids will dissociate in water to form H+ / H3O+ ions
which are free to move. E.g:
i) HCl in liquid methylbenzene (organic solvent) - does not show acidic properties.
ii) HCl in water – show acidic properties
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ROLE OF WATER TO SHOW PROPERTIES ROLE OF WATER TO SHOW PROPERTIES OF ALKALIOF ALKALI
• Dry base does not show alkaline properties
hydroxide ions (OH-) are not free to move
• In water, bases dissociate form hydroxide ions, OH-, which are free to move
• For example:
i) ammonia in tetrachlomethane (organic solvent) – do not show alkaline properties
ii) ammonia in water – show alkaline properties
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DEFINITION OF ACID AND BASE
Arrhenius Brønsted-Lowry
Lewis
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Arrhenius acid - substance that produces H+ (hydrogen ion) or hydronium ion (H3O+) in water
Arrhenius base - substance that produces OH- in water
DEFINITION OF ACID AND BASE BY ARRHENIUS
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Examples of acid:
CO2 (g) + H2O (l) H2CO3 (aq)
H2CO3 (aq) + H2O(l) H3O+ (aq) + HCO3- (aq)
nonmetal oxides + H2O acid
Examples of bases:
NaOH (s) Na+ (aq) + OH- (aq)
N2H4 (aq) + H2O N2H5+ (aq) + OH- (aq)
metal oxides + H2O bases
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• A Brønsted acid is a proton donor• A Brønsted base is a proton acceptor• Example:
acid base acid base
• A Brønsted acid must contain at least one ionizable proton!
DEFINITION OF ACID AND BASE BY BRØNSTED-LOWRY
HCl (aq) +H2O (l) → H3O+ (aq) + Cl- (aq)
• HCl is a acid because it donates proton to H2O
• H2O is a base because it accepts proton from HCl
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Conjugate acid-base pair:
i) Conjugate base of a Brønsted acid - the species that remains when one proton has been removed from
the acid
ii) Conjugate acid - addition of a proton to a Brønsted base
Examples:
HCl (aq) +H2O (l) H3O+ (aq) + Cl- (aq)
acid1 base2 acid2 base1
Cl- is a conjugate base of HCl and HCl is a conjugate acid of Cl-
H2O is a base conjugate of H3O+ and H3O+ is a acid conjugate of
H2O
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• When a strong acid react with a strong base in Brønsted acid-base
reaction, it will give a weak conjugate acid and conjugate base.
•Examples:
HCl (aq) + H2O (l) H3O+ (aq) + Cl- (aq) strong acid strong base weak conjugate weak conjugate acid base NH3 (aq) + H2O (l) NH4
+ (aq) + OH- (aq) Weak base weak acid strong conjugate strong conjugate acid base
• H2O can function as acid or base which called amphoteric
• Amphoteric or amphiprotic substance is one that can react as either an acid or base
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Identify each of the following species as a Brønsted acid, base, or both. (a) HI, (b) CH3COO-, (c) H2PO4
-
HI (aq) H+ (aq) + I- (aq) Brønsted acid
CH3COO- (aq) + H+ (aq) CH3COOH (aq) Brønsted base
H2PO4- (aq) H+ (aq) + HPO4
2- (aq)
H2PO4- (aq) + H+ (aq) H3PO4 (aq)
Brønsted acid
Brønsted base
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• Lewis acid - substance that can accept a pair of electrons
• Lewis base - substance that can donate a pair of electrons
H+ H O H••••
+ OH-••••••
acid base
N H••
H
H
H+ +
acid base
N H
H
H
H+
DEFINITION OF ACID AND BASE BY LEWIS
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Examples of Lewis Acids and Bases reactions:
N H••
H
H
acid base
F B
F
F
+ F B
F
F
N H
H
Ha)
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ACIDS
i) Strong acids- Acids that completely ionized in solution. - Example:
HCl (aq) → H+ (aq) + Cl- (aq)
ii) Weak acids- Acids that incompletely ionized in solution- Example:
CH3COOH (aq) CH3COO- (aq) + H+ (aq)
TYPES OF ACIDS-BASES
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Monoprotic acid:
- each unit of the acid yields one hydrogen ion upon ionization
HCl H+ + Cl-
HNO3 H+ + NO3-
CH3COOH H+ + CH3COO-
Strong electrolyte, strong acid
Strong electrolyte, strong acid
Weak electrolyte, weak acid
Diprotic acid:
- each unit of the acid gives up two H+ ions, in two separate steps
H2SO4 H+ + HSO4-
HSO4- H+ + SO4
2-
Strong electrolyte, strong acid
Weak electrolyte, weak acid
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Triprotic acids: - yield three H+ ions
H3PO4 H+ + H2PO4-
H2PO4- H+ + HPO4
2-
HPO42- H+ + PO4
3-
Weak electrolyte, weak acidWeak electrolyte, weak acidWeak electrolyte, weak acid
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• BASES
i) Strong bases- Bases that completely ionized in solution. - Example:
NaOH (s) → Na+ (aq) + OH- (aq)
ii) Weak bases- bases that incompletely ionized in solution- Example:
NH3 (aq) + H2O (l) NH4+ (aq) + OH- (aq)
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ACIDS AND BASES AS ACIDS AND BASES AS ELECTROLYTESELECTROLYTES
Strong acids (HCl,HNO3 ) - strong electrolytes
Weak acid (CH3COOH) - weak electrolyte
HCl (aq) + H2O (l) H3O+ (aq) + Cl- (aq)
HNO3 (aq) + H2O (l) H3O+ (aq) + NO3- (aq)
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Strong Bases are strong electrolytes
NaOH (s) Na+ (aq) + OH- (aq)H2O
KOH (s) K+ (aq) + OH- (aq)H2O
Ba(OH)2 (s) Ba2+ (aq) + 2OH- (aq)H2O
F- (aq) + H2O (l) OH- (aq) + HF (aq)
Weak Bases are weak electrolytes
NO2- (aq) + H2O (l) OH- (aq) + HNO2 (aq)
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H2O (l) H+ (aq) + OH- (aq)
autoionization of water
• Can act either as a acid or as a base.
• Water is a very weak electrolyte and undergo ionization to a small extent:
ACID-BASE PROPERTIES OF WATER
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pH = -log [H+]
[H+] = [OH-]
[H+] > [OH-]
[H+] < [OH-]
Solution Is
neutral
acidic
basic
[H+] = 1 x 10-7
[H+] > 1 x 10-7
[H+] < 1 x 10-7
pH = 7
pH < 7
pH > 7
At 250C
pH-A MEASURE OF ACIDITY
• pH – the negative logarithm of the hydrogen in
concentration (in mol/L)
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pOH = -log [OH-]
[H+][OH-] = Kw = 1.0 x 10-14
-log [H+] – log [OH-] = 14.00
pH + pOH = 14.00
Other important relationships
pH Meter
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1) The pH of rainwater collected in a certain region of the northeastern United States on a particular day was 4.82. What is the H+ ion concentration of the rainwater?
pH = -log [H+]
[H+] = 10-pH = 10-4.82 = 1.5 x 10-5 M
2) The OH- ion concentration of a blood sample is 2.5 x 10-7 M. What is the pH of the blood?
pH + pOH = 14.00
pOH = -log [OH-] = -log (2.5 x 10-7) = 6.60
pH = 14.00 – pOH = 14.00 – 6.60 = 7.40
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CALCULATION OF PH FOR CALCULATION OF PH FOR SOLUTION CONTAINING A SOLUTION CONTAINING A
STRONG ACID AND A STRONG ACID AND A SOLUTION OF A STRONG SOLUTION OF A STRONG
BASEBASE
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1) What is the pH of a 0.002 M HNO3 solution?
HNO3 is a strong acid – 100% dissociation.
HNO3 (aq) + H2O (l) H3O+ (aq) + NO3- (aq)
pH = -log [H+] = -log [H3O+] = -log(0.002) = 2.7
Start
End
0.002 M
0.002 M 0.002 M0.0 M
0.0 M 0.0 M
2) What is the pH of a 1.8 x 10-2 M Ba(OH)2 solution?
Ba(OH)2 is a strong base – 100% dissociation.
Ba(OH)2 (s) Ba2+ (aq) + 2OH- (aq)Start
End
0.018 M
0.018 M 0.036 M0.0 M
0.0 M 0.0 M
pH = 14.00 – pOH = 14.00 + log(0.036) = 12.6
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•Concentration - amount of solute present in a given quantity of solvent or solution.
M = molarity =moles of solute
liters of solution
1) What mass of KI is required to make 500 mL of a 2.80 M KI solution?
volume of KI solution moles KI grams KIM KI M KI
500 mL = 232 g KI166 g KI
1 mol KIx
2.80 mol KI
1 L solnx
1 L
1000 mLx
CONCENTRATION OF SOLUTION
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Preparing a Solution of Known Concentration
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Dilution - procedure for preparing a less concentrated solution from a more concentrated solution.
DilutionAdd Solvent
Moles of solutebefore dilution (i)
Moles of soluteafter dilution (f)=
MiVi MfVf=
DILUTION OF DILUTION OF SOLUTIONSSOLUTIONS
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EXAMPLE:
1) How would you prepare 60.0 mL of 0.200 M HNO3 from a stock solution of 4.00 M HNO3?
M1V1 = M2V2
M1 = 4.00 M M2 = 0.200 M V2 = 0.0600 L V1 = ? L
V1 =M2V2
M1
=0.200 M x 0.0600 L
4.00 M = 0.00300 L = 3.00 mL
Dilute 3.00 mL of acid with water to a total volume of 60.0 mL.
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Concentration UnitsConcentration Units
Percent by Mass (%w/w)
% by mass = x 100%mass of solute
mass of solute + mass of solvent
= x 100%mass of solutemass of solution
Percent by Volume (%v/v)
% by volume = x 100%Volume of soluteVolume of solution
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M =moles of solute
liters of solution
Molarity (M)
Molality (m)
m =moles of solute
mass of solvent (kg)
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• In a titration a solution of accurately known concentration (standard solution) is added gradually added to another solution of unknown concentration until the chemical reaction between the two solutions is complete.
• Equivalence point – the point at which the reaction is complete
• Indicator – substance that changes color at (or near) the equivalence point
TITRATIONS
• Titrations can be used in the analysis of acid-base reactions
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Slowly add baseto unknown acid
UNTIL
the indicatorchanges color
PROCEDURE FOR THE TITRATION PROCEDURE FOR THE TITRATION
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EXAMPLE:1) What volume of a 1.420 M NaOH solution is required to titrate 25.00 mL of a 4.50 M H2SO4 solution?
WRITE THE CHEMICAL EQUATION!
H2SO4 + 2NaOH 2H2O + Na2SO4
MaVa
MbVb
=a
b
Ma = concentration of acidMb = concentration of baseVa = volume of acidVb = volume of basea = coefficient of acidb = coefficient of base
(4.50 M) (25 mL)
(1.420 M) (Vb)=
1
2
Vb = 158 mL
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ACID-BASE TITRATIONSStrong Acid-Strong Base Titrations
NaOH (aq) + HCl (aq) H2O (l) + NaCl (aq)
OH- (aq) + H+ (aq) H2O (l)
pH PROFILE OF THE TITRATION (TITRATION CURVE)pH PROFILE OF THE TITRATION (TITRATION CURVE)
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• Before addition of NaOH
- pH = 1.00
• When the NaOH added
- pH increase slowly at first
• Near the equivalence point
- the curve rises almost vertically
• Beyond the equivalence point
- pH increases slowly
pH PROFILE OF THE TITRATION pH PROFILE OF THE TITRATION (TITRATION CURVE) (TITRATION CURVE)
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CALCULATION OF PH AT EVERY STAGE OF CALCULATION OF PH AT EVERY STAGE OF TITRATIONTITRATION
1) After addition of 10.0 mL of 0.100 M NaOH to 25.0 mL of 0.100 M HCl
Total volume = 35.0 mL
Moles of NaOH in 10.0 mL
= 10.0 mL x 0.100 mol NaOH x 1L
1L NaOH 1000 mL
= 1.00 x 10-3 mol
Moles of HCl in 25.0 mL
= 25.0 mL x 0.100 mol HCl x 1L
1 L HCl 1000 mL
= 2.50 x 10-3 mol
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Amount of HCl left after partial neutralization
= (2.50 x 10-3)-(1.00 x 10-3)
= 1.50 x 10-3 mol
Concentration of H+ ions in 35.0 mL
1.50 x 10-3 mol HCl x 1000 mL = 0.0429 M HCl
35.0 mL 1L
[H+] = 0.0429 M,
pH = -log 0.0429 = 1.37
2) After addition of 25.0 mL of 0.100 M NaOH to 25.0 mL 0f 0.100 M HCl[H+] = [OH-] = 1.00 x 10-7
pH = 7.00
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3) After addition of 35.0 mL of 0.100 M NaOH to 25.0 mL of 0.100 mL of HCl
Total volume = 60.0 mLMoles of NaOH added= 35.0 mL x 0.100 mol NaOH x 1L 1 L NaOH 1000 mL= 3.50 x 10-3 mol
Moles of HCl in 25.0 mL solution = 2.50 x 10-3 molAfter complete neutralization of HCl, no of moles of NaOH left = (3.50 x 10-3)-(2.50x10-3)= 1.00 x 10-3 mol
Concentration of NaOH in 60.0 mL solution= 1.00 x 10-3 mol NaOH x 1000 mL 60.0 mL 1L= 0.0167 M NaOH[OH-] = 0.0167 MpOH = -log 0.0167 = 1.78pH = 14.00 – 1.78 = 12.22