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Edexcel AS Chemistry

Revision Notes

Home / AS / Chemistry / Edexcel / Revision Notes / 1. Physical Chemistry / 1.6 Formulae, Equations & Avogadro / 1.6.4 The Mole & the Avogadro Constant


1.6.4 The Mole & the Avogadro Constant


The Mole & Avogadro

  • The Avogadro constant (NA or L) is the number of particles equivalent to the relative atomic mass or molecular mass of a substance
    • The Avogadro constant applies to atoms, molecules, ions and electrons

  • The value of NA is 6.02 x 1023 g mol-1
  • The mass of a substance with this number of particles is called a mole (mol)
    • This can be called the molar mass 
    • This is the mass of substance that contains the same number of fundamental units as exactly 12.00g of carbon-12
  • The amount / number of moles of a substance, n, the mass of the substance, m, and the molar mass, M, are linked by the equation:

n = fraction numerator m a s s comma space m over denominator M o l a r space m a s s comma space M end fraction

  • One mole of any element is equal to the relative atomic mass of that element in grams
    • If you had one mole of carbon in your hand, that is 6.02 x 1023 atoms of carbon, you would have a mass of 12.00 g
    • One mole of water would have a mass of (2 x 1 + 16) = 18 g

Worked Example

  1. What is the molar mass of water?
  2. How many moles are there in 100 g of water?
  3. How many water molecules are there in 100 g of water?

Answers

    1. Molar mass of water, H2O = (2 x 1.0) + 16.0 = 18.0 g mol-1 
    2. Moles equals fraction numerator m a s s over denominator m o l a r space m a s s end fraction space equals space fraction numerator 100 over denominator 18.0 end fraction space equals5.56 moles (to 3 s.f.)
    3. Number of molecules = number of moles x Avogadro's constant = 5.56 x (6.02 x 1023) = 3.35 x 1024 molecules

Worked Example

What is the mass of the following:

  1. Five hundred million atoms of platinum
  2. (1.31 x 1022) molecules of ethanol

Answer 1:

Number of moles equals space fraction numerator number space of space particles over denominator Avogadro apostrophe straight s space constant comma space straight N subscript straight A end fraction space equals space fraction numerator 500 space cross times 10 to the power of 6 over denominator 6.02 space cross times 10 to the power of 23 end fraction space equals8.31 x10-16 moles

Mass = moles x molar mass = (8.31 x10-16) x 195.1 = 1.62 x 10-13 g (lots of atoms, a tiny mass)

Answer 2:

Molar mass of ethanol, C2H5OH = (2 x 12.0) + (5 x 1.0) + 16.0 + 1.0 = 46.0 g mol-1 

Number of moles equals space fraction numerator number space of space particles over denominator Avogadro apostrophe straight s space constant comma space straight N subscript straight A end fraction space equals space fraction numerator 1.31 space cross times space 10 to the power of 22 over denominator 6.02 space cross times 10 to the power of 23 end fraction space equals0.0218 moles

Mass = moles x molar mass = 0.0218 x 46.0 = 1.00 g (an exceptionally large number of molecules in just 1 g)

Exam Tip

  • When you are completing calculations using Avogadro's constant, you may end up with answers that seem very large or very small - don't automatically assume that they must be wrong
  • Remember, Avogadro's constant is a VERY large number:
    • 6.02 x 1023 or 602 000 000 000 000 000 000 000
  • So when you multiply or divide by Avogadro's constant, your answers will, naturally, become very large or very small


  • 1. Physical Chemistry
    • 1.1 Atomic Structure
      • 1.1.1 Structure of the Atom
        • 1.1.2 Isotopes
          • 1.1.3 Relative Mass
            • 1.1.4 Mass Spectrometry
            • 1.2 Ions & Electrons
              • 1.2.1 Ionisation Energy
                • 1.2.2 Quantum Shells
                  • 1.2.4 Electronic Configurations
                  • 1.3 The Periodic Table
                    • 1.3.1 Periodicity
                    • 1.4 Bonding
                      • 1.4.1 Ionic Bonding Overview
                        • 1.4.2 Representing Ionic Bonding
                          • 1.4.3 Ionic Trends
                            • 1.4.4 Physical Properties of Ionic Compounds
                              • 1.4.5 Covalent Bonding Overview
                                • 1.4.6 Covalent Dot-and-Cross Diagrams
                                  • 1.4.7 Bond Length & Bond Strength
                                    • 1.4.8 Shapes of Covalent Compounds
                                    • 1.5 Structure
                                      • 1.5.1 Electronegativity
                                        • 1.5.2 Intermolecular Forces
                                          • 1.5.3 Hydrogen Bonding
                                            • 1.5.4 Intermolecular Forces & Physical Properties
                                              • 1.5.5 Metallic Bonding
                                                • 1.5.6 Giant Lattices
                                                  • 1.5.7 Covalent Structures
                                                    • 1.5.8 Predicting Structures
                                                    • 1.6 Formulae, Equations & Avogadro
                                                      • 1.6.1 Empirical & Molecular Formulae
                                                        • 1.6.4 The Mole & the Avogadro Constant
                                                        • 1.7 Reaction Calculations
                                                          • 1.7.1 Reacting Volume Calculations
                                                            • 1.7.2 Titrations
                                                              • 1.7.3 Error & Uncertainty
                                                                • 1.7.4 Yield & Atom Economy
                                                                • 1.8 Energetics I
                                                                  • 1.8.1 Enthalpy Changes
                                                                    • 1.8.3 Calorimetry
                                                                      • 1.8.4 Hess Cycles
                                                                        • 1.8.5 Bond Enthalpy
                                                                          • Enthalpy Level Diagrams
                                                                          • 1.9 Kinetics
                                                                            • 1.9.1 Collision Theory & Rates
                                                                              • 1.9.2 Calculating Rates of Reaction
                                                                                • 1.9.3 Maxwell-Boltzmann Distributions
                                                                                  • 1.9.4 Catalysts in Industry
                                                                                  • 1.10 Equilibrium I
                                                                                    • 1.10.2 Le Chatelier's Principle
                                                                                      • 1.10.3 The Rate & Yield Compromise
                                                                                        • 1.10.4 Deducing Kc Expressions
                                                                                      • 2. Inorganic Chemistry
                                                                                        • 2.1 Redox I
                                                                                          • 2.1.1 Oxidation Number
                                                                                            • 2.1.2 Types of Reduction & Oxidation
                                                                                              • 2.1.3 Redox & Disproportionation
                                                                                                • 2.1.4 Ionic Equations
                                                                                                • 2.2 Groups 1 & 2
                                                                                                  • 2.2.1 Explaining Group 2 Trends
                                                                                                    • 2.2.2 Reactions of Group 2
                                                                                                      • 2.2.3 Group 2 Hydroxides & Sulfates
                                                                                                        • 2.2.4 Group 2 Carbonates & Nitrates
                                                                                                          • 2.2.5 Flame Tests
                                                                                                          • 2.3 Group 7
                                                                                                            • 2.3.1 Group 7 Trends
                                                                                                              • 2.3.2 Halogen Displacement Reactions
                                                                                                                • 2.3.3 Halogen Redox Reactions
                                                                                                                  • 2.3.4 Halide Ion Reactions
                                                                                                                • 3. Organic Chemistry
                                                                                                                  • 3.1 Introduction to Organic Chemistry
                                                                                                                    • 3.1.1 formulae of organic compounds
                                                                                                                      • 3.1.2 Homologous Series and Functional Groups
                                                                                                                        • 3.1.3 Nomenclature and Classification
                                                                                                                          • 3.1.4 Structural Isomerism
                                                                                                                            • 3.1.5 Stereoisomerism
                                                                                                                            • 3.2 Alkanes
                                                                                                                              • 3.2.1 Describing Alkanes
                                                                                                                                • 3.2.2 Alkane Fuels
                                                                                                                                  • 3.2.3 Pollution from Combustion
                                                                                                                                    • 3.2.4 Reducing Pollution
                                                                                                                                      • 3.2.5 Free Radicals
                                                                                                                                      • 3.3 Alkenes
                                                                                                                                        • 3.3.1 Describing Alkenes
                                                                                                                                          • 3.3.2 Bonding in Alkenes
                                                                                                                                            • 3.3.3 Electrophilic addition
                                                                                                                                              • 3.3.4 Electrophilic Addition Mechanism
                                                                                                                                                • 3.3.5 Saturation Test
                                                                                                                                                  • 3.3.6 Addition Polymerisation
                                                                                                                                                    • 3.3.7 Waste Polymers
                                                                                                                                                    • 3.4 Halogenoalkanes
                                                                                                                                                      • 3.4.1 Classifying Halogenoalkanes
                                                                                                                                                        • 3.4.2 Nucleophilic Substitution
                                                                                                                                                          • 3.4.3 Nucleophilic Substitution Mechanism
                                                                                                                                                            • 3.4.4 Hydrolysis of Halogenoalkanes
                                                                                                                                                              • 3.4.5 Reactivity of Halogenoalkanes
                                                                                                                                                              • 3.5 Alcohols
                                                                                                                                                                • 3.5.1 Classifying Alcohols
                                                                                                                                                                  • 3.5.2 Reactions of Alcohols
                                                                                                                                                                    • 3.5.3 Organic Liquid Preparation & Purification
                                                                                                                                                                    • 3.6 Modern Analytical Techniques I
                                                                                                                                                                      • 3.6.1 Mass Spectrometry
                                                                                                                                                                        • 3.6.2 Infrared (IR) Spectroscopy
                                                                                                                                                                      • 4. Core Chemistry Practicals
                                                                                                                                                                        • 4.1 Physical Chemistry Core Practicals
                                                                                                                                                                          • 4.1.1 Molar Volume of a Gas
                                                                                                                                                                            • 4.1.2 Standard Solutions
                                                                                                                                                                              • 4.1.3 Determining Concentrations
                                                                                                                                                                                • 4.1.4 Determining Enthalpy Change of Reaction
                                                                                                                                                                                • 4.2 Inorganic & Organic Chemistry Core Practicals
                                                                                                                                                                                  • 4.2.1 Hydrolysis of Halogenoalkanes
                                                                                                                                                                                    • 4.2.2 Ethanol Oxidation
                                                                                                                                                                                      • 4.2.3 Chlorination of 2-Methylpropan-2-ol
                                                                                                                                                                                        • 4.2.4 Qualitative Analysis


                                                                                                                                                                                        DOWNLOAD PDF

                                                                                                                                                                                      Author: Richard

                                                                                                                                                                                      Richard has taught Chemistry for over 15 years as well as working as a science tutor, examiner, content creator and author. He wasn’t the greatest at exams and only discovered how to revise in his final year at university. That knowledge made him want to help students learn how to revise, challenge them to think about what they actually know and hopefully succeed; so here he is, happily, at SME.


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