2.5.7

Buffer Solutions (A2 Only)

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Buffer Solutions

Buffer solutions oppose small changes in pH.

What is a buffer solution?

What is a buffer solution?

  • A buffer solution is a solution that opposes pH changes.
    • This means that if you add acid, the buffer solution removes it to keep a constant pH.
    • In reality, they don't keep a completely constant pH, but they reduce the size of any changes.
How does a buffer solutions work?

How does a buffer solutions work?

  • Buffers work through changes in equilibria.
  • An acidic buffer will contain a weak acid and a salt of the weak acid.
    • E.g. methanoic acid and sodium methanoate.
  • The important equilibrium is:
    • CHOOH ⇌ CHOO- + H+
  • As you have sodium methanoate, you have lots of CHOO-.
  • According to le Chatelier’s principle, this will remove lots of H+ from solution to reduce the concentration of CHOO-.
    • This means you have a lot of un-ionised methanoic acid
Adding acid to an acid buffer

Adding acid to an acid buffer

  • If you add acid to this acid buffer solution, then the methanoate ions will react with the hydrogen ions and remove them.
    • This will reduce any change in pH.
Adding a base to an acid buffer

Adding a base to an acid buffer

  • If you add a base to the acid buffer solution, the hydrogen ions will react with it and neutralise it.
  • The un-ionised methanoic acid will ionise to produce more H+ ions and this will reduce the pH change.
Basic buffers

Basic buffers

  • A basic buffer has a pH above 7 and works on a similar principle.
  • A good example is ammonium hydroxide.
  • The equilibrium for this reaction is:
    • NH3 + H2O ⇌ NH4+ + OH-
    • Adding base shifts the equilibrium left to remove base.
    • Adding acid shifts the equilibrium right to remove the acid.

Calculations of Buffer Solutions

Buffer solutions have a specific pH, which can be calculated.

Assumptions

Assumptions

  • All you need to know to calculate the pH of a buffer solution is its Ka.
  • You need to make a couple of reasonable assumptions:
    • That the salt is fully dissociated.
    • That the acid is pretty much un-ionised.
Method

Method

  • Write down the equation for Ka:
    • Ka = [H+][A−][HA]\frac{[H^+][A^-]}{[HA]}
  • Rearrange it for the hydrogen ion concentration:
    • [H+] = Ka × [HA][A−]\frac{[HA]}{[A^-]}
  • We assume the salt is fully dissociated, so [A-] is just the inital salt concentration.
  • We assume the [HA] is un-ionised, so that’s just the initial acid concentration.
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1

Physical Chemistry

1.1

Atomic Structure

1.1.1Fundamental Particles1.1.2Isotopes & Mass Number1.1.3Mass Spectrometry1.1.4Electron Shells, Sub-Shells & Orbitals1.1.5Electron Configuration1.1.6Ionisation Energy1.1.7Factors Affecting Ionisation Energies1.1.8Trends of Ionisation1.1.9Specific Impacts on Ionisation Energies1.1.10End of Topic Test - Atomic Structure1.1.11A-A* (AO3/4) - Atomic Structure
1.2

Amount of Substance

1.2.1Relative Masses1.2.2The Mole1.2.3The Ideal Gas Equation1.2.4Empirical & Molecular Formulae1.2.5Balanced Equations1.2.6Percentage Yield1.2.7A-A* (AO3/4) - Percentage Yield1.2.8Atom Economy1.2.9End of Topic Test - Amount of Substance1.2.10A-A* (AO3/4) - Substances & Yield1.2.11Diagnostic Misconceptions - Moles
1.3

Bonding

1.3.1Ionic Bonding1.3.2Covalent & Dative Bonding1.3.3Carbon Structures1.3.4Metallic Bonding1.3.5Physical Properties1.3.6Shapes of Molecules1.3.7Polarity1.3.8Intermolecular Forces1.3.9Intermolecular Forces 21.3.10End of Topic Test - Bonding1.3.11Exam-Style Question - Shape of Molecules1.3.12A-A* (AO3/4) - Bonding1.3.13Diagnostic Misconceptions - Ions1.3.14Diagnostic Misconceptions - Ionic & Covalent1.3.15Diagnostic Misconceptions - Phase Change1.3.16Diagnostic Misconceptions - Boiling1.3.17Diagnostic Misconceptions - Polar Bonds
1.4

Energetics

1.4.1Enthalpy Changes1.4.2Bond Breaking and Making1.4.3Enthalpy Changes: Standard Conditions1.4.4Calorimetry1.4.5Hess' Law1.4.6Bond Enthalpies1.4.7End of Topic Test - Energetics1.4.8Diagnostic Misconceptions - Calorimetry
1.5

Kinetics

1.5.1Collision Theory1.5.2Maxwell-Boltzmann Distribution1.5.3Increasing Rates1.5.4End of Topic Test - Kinetics
1.6

Equilibria

1.6.1Le Chatelier1.6.2Equilibrium Constants1.6.3A-A* (AO3/4) - Energetics, Kinetics, Equilibria1.6.4End of Topic Test - Equilibria1.6.5Diagnostic Misconceptions - Solids
1.7

Redox

1.7.1Redox1.7.2End of Topic Test - Redox
2

Physical Chemistry 2 (A2 Only)

2.1

Thermodynamics (A2 Only)

2.1.1Born-Haber Cycles (A2 Only)2.1.2Born-Haber Cycle Calculations (A2 Only)2.1.3Entropy (A2 Only)2.1.4Free Energy (A2 Only)2.1.5End of Topic Test - Thermodynamics2.1.6A-A* (AO3/4) - Thermodynamics
2.2

Rate Equations (A2 Only)

2.2.1Rate Equations (A2 Only)2.2.2Rate Equations 2 (A2 Only)2.2.3The Arrhenius Equation (A2 Only)2.2.4Experimental Methods for Rates (A2 Only)2.2.5End of Topic Test - Rate Equations2.2.6Exam-Style Question - Rates2.2.7A-A* (AO3/4) - Rate Equations
2.3

The Equilibrium Constant Kp (A2 Only)

2.3.1Properties of Kp (A2 Only)
2.4

Electrochemical Cells (A2 Only)

2.4.1Electrochemical Cells (A2 Only)2.4.2Electrochemical Series (A2 Only)2.4.3Commercial Application (A2 Only)2.4.4End of Topic Test - Kp & Electrochemistry2.4.5A-A* (AO3/4) - Electrochemical Cells2.4.6Diagnostic Misconceptions - Salt Bridges2.4.7Diagnostic Misconceptions - Electrode, Electrolyte
2.5

Acids & Bases (A2 Only)

2.5.1Brønsted-Lowry Acids & Bases (A2 Only)2.5.2pH (A2 Only)2.5.3The Ionic Product of Water (A2 Only)2.5.4Weak Acids & Bases (A2 Only)2.5.5pH Curves & Titrations (A2 Only)2.5.6pH Curves & Titrations 2 (A2 Only)2.5.7Buffer Solutions (A2 Only)2.5.8End of Topic Test - Acids & Bases2.5.9Exam-Style Question - Weak Acids2.5.10A-A* (AO3/4) - Acids & Bases2.5.11Diagnostic Misconceptions - Ammonia is an Alkali2.5.12Diagnostic Misconceptions - Water's Neutrality2.5.13Diagnostic Misconceptions - Concentrate & Strength
3

Inorganic Chemistry

3.1

Periodicity & Trends

3.1.1The Periodic Table3.1.2Trends in the Periodic Table3.1.3End of Topic Test - Periodicity & Trends3.1.4Diagnostic Misconceptions - Atomic Radius
3.2

Group 2

3.2.1Group 2 Chemistry3.2.2End of Topic Test - Group 2
3.3

Group 7

3.3.1Introduction to Halogens3.3.2Reactions of Halogens3.3.3Chlorine & Chlorate(I)3.3.4End of Topic Test - Group 73.3.5Exam-Style Question - Group 73.3.6A-A* (AO3/4) - Periodicity, Group 2 & 7
4

Inorganic Chemistry 2 (A2 Only)

4.1

Period 3 (A2 Only)

4.1.1Period 3 Elements & Oxides (A2 Only)4.1.2Period 3 Oxides (A2 Only)4.1.3End of Topic Test - Period 3
4.2

Transition Metals (A2 Only)

4.2.1General Properties (A2 Only)4.2.2Substitution Reactions (A2 Only)4.2.3Shapes of Complex Ions (A2 Only)4.2.4Colours of Ions (A2 Only)4.2.5Variable Oxidation States (A2 Only)4.2.6Titrations (A2 Only)4.2.7Homogeneous Catalysts (A2 Only)4.2.8Heterogeneous Catalysts (A2 Only)4.2.9End of Topic Test - Transition Metals4.2.10A-A* (AO3/4) - Transition Metals
4.3

Reactions of Ions in Aqueous Solutions (A2 Only)

4.3.1Acidity (A2 Only)4.3.2Identification (A2 Only)4.3.3End of Topic Test - Reactions of Ions in Solution
5

Organic Chemistry 1

5.1

Introduction

5.1.1Naming Conventions5.1.2Mechanism5.1.3Isomerism5.1.4End of Topic Test - Introduction to Organic Chem
5.2

Alkanes

5.2.1Fractional Distillation5.2.2Cracking5.2.3Combustion5.2.4Chlorination5.2.5End of Topic Test - Alkanes
5.3

Halogenoalkanes

5.3.1Substitution Reactions5.3.2Elimination Reactions5.3.3Ozone Depletion5.3.4End of Topic Test - Halogenoalkanes
5.4

Alkenes

5.4.1Introduction to Alkenes5.4.2Reactions of Alkenes5.4.3Polymerisation Reactions5.4.4Properties of Polymers5.4.5End of Topic Test - Alkenes
5.5

Alcohols

5.5.1Production of Alcohols5.5.2Oxidation of Alcohols5.5.3Oxidation of Alcohols - 25.5.4Elimination Reactions5.5.5End of Topic Test - Alcohols5.5.6Exam-Style Question - Alcohols
5.6

Organic Analysis

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5.7

A-A* (AO3/4) - Organic 1

5.7.1A-A* (AO3/4) - Organic 1
6

Organic Chemistry 2 (A2 Only)

6.1

Optical Isomerism (A2 Only)

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6.2

Aldehydes & Ketones (A2 Only)

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6.3

Carboxylic Acids & Esters (A2 Only)

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6.4

Aromatic Chemistry (A2 Only)

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6.5

Amines (A2 Only)

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6.6

Polymers (A2 Only)

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6.7

Biological Organic (A2 Only)

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6.8

Organic Synthesis (A2 Only)

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6.9

NMR Spectroscopy (A2 Only)

6.9.1Understanding NMR (A2 Only)6.9.2Carbon-13 NMR (A2 Only)6.9.3Hydrogen-1 NMR (A2 Only)6.9.4Hydrogen-1 NMR 2 (A2 Only)6.9.5End of Topic Test - NMR
6.10

Chromatography (A2 Only)

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6.11

A-A* (AO3/4) - Organic 2

6.11.1A-A* (AO3/4) - Organic 2

Practice questions on Buffer Solutions (A2 Only)

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  1. 1
    An example of weak acid and its salt is methanoic acid and sodium methanoate. The important equilibrium is:Multiple choice
  2. 2
    What happens when you add an acid to an acid buffer?True / false
  3. 3
    For the basic buffer ammonium hydroxide<br> NH<sub>3</sub> + H<sub>2</sub>O &rightleftharpoons; NH<sub>4</sub><sup>+</sup> + OH<sup>-</sup>:Fill in the list
  4. 4
    What do you need to know to calculate the pH of a buffer solution?Multiple choice
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pH Curves & Titrations 2 (A2 Only)

End of Topic Test - Acids & Bases