Burrows, Holman, Lancaster, Overton, Parsons, Pilling & Price, Chemistry³ 4e Student resources

Description

The following student resources are available for this title:

Chapter learning outcomes, summaries, and key equations
Solutions manuals for questions in the book
Video clips
Screencasts for each chapter
Self-test multiple choice questions for each chapter
ChemTube3D interactive molecular structures
Maths self-test questions
Access to the enhanced e-book

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Maths self-test questions
Self-test Questions

Chemistry³ 4e e-Book

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Chapter 1 learning outcomes, summaries, and key equations

Fundamentals

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Chapter 2 Chapter learning outcomes, summaries, and key equations

The language of organic chemistry

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Chapter 3 Chapter learning outcomes, summaries, and key equations

Atomic structure and properties

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Chapter 4 Chapter learning outcomes, summaries, and key equations

Diatomic molecules

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Chapter 5 Chapter learning outcomes, summaries, and key equations

Polyatomic molecules

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Chapter 6 Chapter learning outcomes, summaries, and key equations

Solids

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Chapter 7 Chapter learning outcomes, summaries, and key equations

Acids and bases

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Chapter 8 Chapter learning outcomes, summaries, and key equations

Gases

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Chapter 9 Chapter learning outcomes, summaries, and key equations

Reaction kinetics

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Chapter 10 Chapter learning outcomes, summaries, and key equations

Molecular spectroscopy

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Chapter 11 Chapter learning outcomes, summaries, and key equations

Analytical chemistry

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Chapter 12 Chapter learning outcomes, summaries, and key equations

Molecular characterisation

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Chapter 13 Chapter learning outcomes, summaries, and key equations

Energy and thermochemistry

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Chapter 14 Chapter learning outcomes, summaries, and key equations

Entropy and Gibbs energy

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Chapter 15 Chapter learning outcomes, summaries, and key equations

Chemical equilibrium

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Chapter 16 Chapter learning outcomes, summaries, and key equations

Electrochemistry

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Chapter 17 Chapter learning outcomes, summaries, and key equations

Phase equilibrium and solutions

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Chapter 18 Chapter learning outcomes, summaries, and key equations

Isomerism and stereochemistry

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Chapter 19 Chapter learning outcomes, summaries, and key equations

Organic reaction mechanisms

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Chapter 20 Chapter learning outcomes, summaries, and key equations

Halogenoalkanes: substitution and elimination reactions

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Chapter 21 Chapter learning outcomes, summaries, and key equations

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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Chapter 22 Chapter learning outcomes, summaries, and key equations

Benzene and other aromatic compounds: electrophilic substitution reactions

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Chapter 23 Chapter learning outcomes, summaries, and key equations

Aldehydes and ketones: nucleophilic addition and α-substitution reactions

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Chapter 24 Chapter learning outcomes, summaries, and key equations

Carboxylic acids and derivatives: nucleophilic acyl substitution and α-substitution reactions

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Chapter 25 Chapter learning outcomes, summaries, and key equations

Hydrogen

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Chapter 26 Chapter learning outcomes, summaries, and key equations

s-Block chemistry

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Chapter 27 Chapter learning outcomes, summaries, and key equations

p-Block chemistry

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Chapter 28 Chapter learning outcomes, summaries, and key equations

d-Block chemistry

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Chapter 1 Solutions manual for questions in the book

Fundamentals

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Chapter 2 Solutions manual for questions in the book

The language of organic chemistry

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Chapter 3 Solutions manual for questions in the book

Atomic structure and properties

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Chapter 4 Solutions manual for questions in the book

Diatomic molecules

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Chapter 5 Solutions manual for questions in the book

Polyatomic molecules

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Chapter 6 Solutions manual for questions in the book

Solids

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Chapter 7 Solutions manual for questions in the book

Acids and bases

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Chapter 8 Solutions manual for questions in the book

Gases

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Chapter 9 Solutions manual for questions in the book

Reaction kinetics

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Chapter 10 Solutions manual for questions in the book

Molecular spectroscopy

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Chapter 11 Solutions manual for questions in the book

Analytical chemistry

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Chapter 12 Solutions manual for questions in the book

Molecular characterisation

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Chapter 13 Solutions manual for questions in the book

Energy and thermochemistry

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Chapter 14 Solutions manual for questions in the book

Entropy and Gibbs energy

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Chapter 15 Solutions manual for questions in the book

Chemical equilibrium

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Chapter 16 Solutions manual for questions in the book

Electrochemistry

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Chapter 17 Solutions manual for questions in the book

Phase equilibrium and solutions

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Chapter 18 Solutions manual for questions in the book

Isomerism and stereochemistry

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Chapter 19 Solutions manual for questions in the book

Organic reaction mechanisms

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Chapter 20 Solutions manual for questions in the book

Halogenoalkanes: substitution and elimination reactions

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Chapter 21 Solutions manual for questions in the book

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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Chapter 22 Solutions manual for questions in the book

Benzene and other aromatic compounds: electrophilic substitution reactions

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Chapter 23 Solutions manual for questions in the book

Aldehydes and ketones: nucleophilic addition and α-substitution reactions

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Chapter 24 Solutions manual for questions in the book

Carboxylic acids and derivatives: nucleophilic acyl substitution and α-substitution reactions

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Chapter 25 Solutions manual for questions in the book

Hydrogen

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Chapter 26 Solutions manual for questions in the book

s-Block chemistry

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Chapter 27 Solutions manual for questions in the book

p-Block chemistry

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Chapter 28 Solutions manual for questions in the book

d-Block chemistry

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Video 1.1 Effect of temperature on equilibrium

Fundamentals

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Video 1.2 Le Chatelier's Principle

Fundamentals

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Video 10.1 Absorption spectrometer

Molecular spectroscopy

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Video 10.2 Introduction to IR spectroscopy

Molecular spectroscopy

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Video 10.3 Sample preparation for IR spectroscopy

Molecular spectroscopy

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Video 10.4 Introduction to NMR spectroscopy

Molecular spectroscopy

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Video 10.5 Sample preparation for NMR spectroscopy

Molecular spectroscopy

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Video 11.1 Ion-selective electrodes in the laboratory

Analytical chemistry

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Video 11.2 Introduction to gas chromatography

Analytical chemistry

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Video 11.3 Introduction to high-performance liquid chromatography

Analytical chemistry

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Video 13.1: Using abomb calorimeter

Energy and thermochemistry

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Video 17.1: Formation of supercritical carbon dioxide

Phase equilibrium and solutions

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Screencast 1.1 Worked example 1.11 Constructing and balancing a redox equation from half equations

Fundamentals

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Screencast 1.2 Worked example 1.14 Titration calculation

Fundamentals

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Screencast 1.3 Equilibrium constants: concentrations and partial pressures

Fundamentals

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Screencast 1.4 Equilibrium constants

Fundamentals

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Screencast 2.1 How to draw organic compounds: Representations and abbreviations

The language of organic chemistry

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Screencast 2.2 How to draw organic compounds: Chiral centres

The language of organic chemistry

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Screencast 2.3 How to spot functional groups: Example from nature

The language of organic chemistry

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Screencast 2.4 How to spot functional groups: Examples from the lab

The language of organic chemistry

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Screencast 3.1 Wavelength and frequency

Atomic structure and properties

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Screencast 3.2 Schrödinger equation and quantum numbers

Atomic structure and properties

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Screencast 3.3 Electronic configuration of an atom

Atomic structure and properties

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Screencast 4.1 Energy-level diagram for O2

Diatomic molecules

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Screencast 4.2 Origins of s-p mixing

Diatomic molecules

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Screencast 4.3 How to construct the MO energy-level diagram for HF

Diatomic molecules

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Screencast 5.1 Use of VSEPR theory to predict the shape of an SF4 molecule

Polyatomic molecules

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Screencast 5.2 Use of VSEPR theory to work out the shape of a POCl3 molecule

Polyatomic molecules

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Screencast 5.3 Bonding in a XeF2 molecule using molecular orbital theory

Polyatomic molecules

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Screencast 5.4 Bonding in a B2H6 molecule

Polyatomic molecules

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Screencast 6.1 Close packing

Solids

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Screencast 6.2 How to calculate the packing efficiency of a cubic close-packed structure

Solids

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Screencast 6.3 Identifying the interstitial sites in the cubic close-packed structure

Solids

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Screencast 6.4 Calculating the limiting radius ratio

Solids

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Screencast 7.1 Calculating the equilibrium constant for an acid–base reaction

Acids and bases

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Screencast 7.2 Derivation of the Henderson–Hasselbalch equation

Acids and bases

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Screencast 7.3 pH changes in a titration

Acids and bases

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Screencast 8.1 Correct units for the ideal-gas law

Gases

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Screencast 8.2 Kinetic theory and the empirical ideal gas equation

Gases

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Screencast 8.3 Molecular speed and how it links to temperature and molar mass

Gases

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Screencast 8.4 Collision cross-section

Gases

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Screencast 8.5 Mean free path

Gases

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Screencast 8.6 Van der Waals equation

Gases

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Screencast 9.1 Differential and integrated rate equations

Reaction kinetics

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Screencast 9.2 Reaction half-life

Reaction kinetics

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Screencast 9.3 Flash photolysis experiment

Reaction kinetics

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Screencast 9.4 Elementary and complex reactions

Reaction kinetics

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Screencast 9.5 Steady state approximation in deriving rate equations

Reaction kinetics

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Screencast 9.6 Transition state theory

Reaction kinetics

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Screencast 10.1 Boltzmann distribution

Molecular spectroscopy

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Screencast 11.1 pH probes and ion-selective electrodes

Analytical chemistry

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Screencast 12.1: Identifying organic compounds using mass spectrometry

Molecular characterisation

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Screencast 12.2: Identify carbonyl compounds using infrared spectroscopy

Molecular characterisation

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Screencast 12.3: How to assign a 1H NMR spectrum

Molecular characterisation

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Screencast 12.4: How to determine a structure using a combination of spectroscopic techniques

Molecular characterisation

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Screencast 13.1: Variation of enthalpy with temperature

Energy and thermochemistry

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Screencast 13.2: Using the Kirchhoff Equation

Energy and thermochemistry

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Screencast 13.3: Internal energy changes

Energy and thermochemistry

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Screencast 13.4: Relationship between ΔH and ΔU

Energy and thermochemistry

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Screencast 13.5: Bomb calorimeter calculation

Energy and thermochemistry

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Screencast 14.1: Variation of entropy with temperature

Entropy and Gibbs energy

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Screencast 14.2: Calculating the standard entropy of chlorine gas at 298 K

Entropy and Gibbs energy

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Screencast 14.3: Entropy change and Gibbs energy

Entropy and Gibbs energy

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Screencast 14.4: Variation of Gibbs Energy change with temperature

Entropy and Gibbs energy

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Screencast 15.1: Equilibrium constant to Gibbs free energy change

Chemical equilibrium

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Screencast 15.2: Butane/methylpropane calculation

Chemical equilibrium

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Screencast 15.3: Adding a reactant or product to an equilibrium mixture

Chemical equilibrium

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Screencast 15.4: van't Hoff equation

Chemical equilibrium

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Screencast 16.1: Daniell cell

Electrochemistry

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Screencast 16.2: Redox electrodes

Electrochemistry

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Screencast 16.3: Predicting the direction of redox reactions using standard reduction potentials

Electrochemistry

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Screencast 16.4: Nernst equation

Electrochemistry

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Screencast 17.1: Derivation and use of the Clapeyron equation

Phase equilibrium and solutions

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Screencast 17.2: Determining potential energy for two interacting molecules

Phase equilibrium and solutions

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Screencast 17.3: Using Raoult's Law to calculate the vapour pressure of a mixture of two liquids

Phase equilibrium and solutions

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Screencast 17.4: Effect of mixture composition on vapour pressures in liquid mixtures

Phase equilibrium and solutions

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Screencast 17.5: Phase equilibria and the distillation behaviour of azeotropic liquid mixtures

Phase equilibrium and solutions

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Screencast 18.1: Naming substituted alkenes

Screencast 18A: Naming substituted alkenes

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Screencast 18.2: Naming enantiomers

Isomerism and stereochemistry

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Screencast 18.3: How to recognise diastereomers

Isomerism and stereochemistry

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Screencast 18.4: How to recognise diastereoselective reactions

Isomerism and stereochemistry

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Screencast 19.1: How to draw resonance forms

Organic reaction mechanisms

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Screencast 19.2: How to describe reactions using orbitals

Organic reaction mechanisms

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Screencast 19.3: How to draw reaction mechanisms

Organic reaction mechanisms

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Screencast 19.4: How to recognize selectivity in organic reactions

Organic reaction mechanisms

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Screencast 20.1: How to activate alcohols using sulfonyl chlorides

Halogenoalkanes: substitution and elimination reactions

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Screencast 20.2: How to recognise SN1 and SN2 reactions of halogenoalkanes

Halogenoalkanes: substitution and elimination reactions

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Screencast 20.3: How to recognise E1 and E2 reactions of halogenoalkanes

Halogenoalkanes: substitution and elimination reactions

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Screencast 20.4: How to distinguish between substitution and elimination reactions

Halogenoalkanes: substitution and elimination reactions

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Screencast 21.1: How to prepare alkenes by partial reduction of alkynes

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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Screencast 21.2: How to draw mechanisms for electrophilic addition reactions of alkenes

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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Screencast 21.3: How to draw mechanisms for the formation and reactions of epoxides

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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Screencast 21.4: How to draw mechanisms and identify the products from pericyclic reactions of alkenes

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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Screencast 22.1: How to write reaction mechanisms, identify reagents and products for electrophilic substitutions

Benzene and other aromatic compounds: electrophilic substitution reactions

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Screencast 22.2: How to recognise the directing effects of substituents

Benzene and other aromatic compounds: electrophilic substitution reactions

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Screencast 22.3: How to prepare substituted benzenes involving transforming substituents

Benzene and other aromatic compounds: electrophilic substitution reactions

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Screencast 22.4: How to use retrosynthesis to design efficient syntheses of polysubstituted benzenes

Benzene and other aromatic compounds: electrophilic substitution reactions

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Screencast 23.1: How to draw reaction mechanisms for nucleophilic addition reactions of aldehydes and ketones

Aldehydes and ketones: nucleophilic addition and a-substitution reactions

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Screencast 23.2: How to use acetals as protecting groups

Aldehydes and ketones: nucleophilic addition and a-substitution reactions

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Screencast 23.3: How to draw mechanisms of a-substitution reactions of aldehydes and ketones

Aldehydes and ketones: nucleophilic addition and a-substitution reactions

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Screencast 23.4: How to draw mechanisms for aldol condensations

Aldehydes and ketones: nucleophilic addition and a-substitution reactions

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Screencast 24.1: How to draw reaction mechanisms for nucleophilic acyl substitution reactions of esters

Carboxylic acids and derivatives: nucleophilic acyl substitution and a-substitution reactions

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Screencast 24.2: How to draw reaction mechanisms for a-substitution reactions of esters

Carboxylic acids and derivatives: nucleophilic acyl substitution and a-substitution reactions

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Screencast 24.3: How to draw reaction mechanisms for Claisen condensations

Carboxylic acids and derivatives: nucleophilic acyl substitution and a-substitution reactions

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Screencast 24.4: How to draw reaction mechanisms for Dieckmann reactions

Carboxylic acids and derivatives: nucleophilic acyl substitution and a-substitution reactions

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Screencast 25.1: How deuteration affects an infrared spectrum

Hydrogen

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Screencast 26.1: ΔHr for the decomposition of Group 1 peroxides

s-Block chemistry

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Screencast 26.2: Calculating the enthalpy change of formation of Li3N

s-Block chemistry

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Screencast 26.3: Factors affecting solubility of Group 1 salts

s-Block chemistry

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Screencast 26.4: Why magnesium(I) chloride does not exist

s-Block chemistry

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Screencast 27.1: Using bond enthalpies to predict the structure of phosphorus

p-Block chemistry

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Screencast 27.2: Fluxionality of PF5

p-Block chemistry

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Screencast 27.3: Calculations to compare the stability of NF3 and NCl3

p-Block chemistry

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Screencast 28.1: How to determine the electronic configuration of a metal ion

d-Block chemistry

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Screencast 28.2: Octahedral complex: high spin or low spin

d-Block chemistry

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Screencast 28.3: Using magnetic data to determine spin

d-Block chemistry

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ChemTube 3D 3.1 d

Shape of d orbitals

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ChemTube 3D 3.1 p

Shape of p orbitals

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ChemTube 3D 3.1 s

Shape of s orbitals

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ChemTube 3D 6.3 bcc

Body-centred cubic – bcc

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ChemTube 3D 6.3 simple cubic lattice

Primitive cubic – cP

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ChemTube 3D 6.6 antiflourite

Na₂O – Antifluorite

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ChemTube 3D 6.6 fluorite

CaF₂ – Fluorite

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ChemTube 3D 6.8 blende

Sphalerite (zinc blende)

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ChemTube 3D 6.8 wurtzite

Wurtzite

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ChemTube 3D 6.9 cdcl2

CdCl₂ – Cadmium chloride

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ChemTube 3D 6.9 cdi2

CdI₂ – Cadmium iodide

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ChemTube VSEPR CH4 Methane

CH₄ Methane

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ChemTube VSEPR H2O Water

H₂O Water

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ChemTube VSEPR PF5 Phosphorus Pentafluoride

PF_₅ Phosphorus Pentafluoride

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ChemTube VSEPR SF4 Sulfur Tetrafluoride

SF₄ Sulfur Tetrafluoride

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ChemTube3D 19.3: Diels–Alder reaction overview: Introductory pages - dacyclopentadiene and nitroalkene

Identifying a Diels-Alder product

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ChemTube3D 19.3: Diels–Alder reaction overview: Introductory pages - dadieneester

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ChemTube3D 19.3: Diels–Alder reaction overview: Reaction gallery - asymauxdaphmenthol-4

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ChemTube3D 19.3: Diels–Alder reaction overview: Reaction gallery - da11-dimethylbutadiene_and_methylmethacrylate

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ChemTube3D 19.3: Diels–Alder reaction overview: Reaction gallery - daacrolein

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ChemTube3D 19.3: Diels–Alder reaction overview: Reaction gallery - dadienequinone

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ChemTube3D 19.3: Diels–Alder reaction overview: Reaction gallery - dahexa-24-diene_and_acrolein

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ChemTube3D 19.3: Diels–Alder reaction overview: Reaction gallery - daintraester

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ChemTube3D 19.3: Diels–Alder reaction overview: Reaction gallery - dapyrone

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ChemTube3D 19.3: Diels–Alder reaction overview: Reaction gallery - datrapping_reactive_intermediates

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ChemTube3D 19.3: Diels–Alder reaction overview: Regioselectivity - cycloaddition2

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ChemTube3D 19.3: Diels–Alder reaction overview: Regioselectivity - daregioselectivity

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - da_dead

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - dacyclopentadiene_alkynediester

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - dadiene_alkynediester

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - diels-alder-stereochemistry-of-the-diene

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - diels-alder-stereochemistry-of-the-diene-cis-cis

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - diels-alder-stereochemistry-of-the-diene-cis-trans

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - diels-alder-stereochemistry-of-the-diene-trans-trans

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - diels-alder-stereochemistry-of-the-dienophile

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ChemTube3D 19.3: Diels–Alder reaction overview: Stereochemistry - diels-alder_-_stereochemistry_of_the_dienophile

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ChemTube3D 19.3: Diels–Alder reaction overview: The Diels-Alder reaction – the endo rule - cycloaddition1

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ChemTube3D 19.3: Diels–Alder reaction overview: The Diels-Alder reaction – the endo rule - da_endo_vs_exo2

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ChemTube3D 19.3: Diels–Alder reaction overview: The Diels-Alder reaction – the endo rule - daendo_vs_exocyclopentadiene_and_maleic_anhydride

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ChemTube3D 19.3: Diels–Alder reaction overview: The Diels-Alder reaction – the endo rule - daintra

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ChemTube3D 19.3: Diels–Alder reaction overview: The Diels-Alder reaction – the endo rule - daintramolecular_reaction

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ChemTube3D 19.3: Diels–Alder reaction overview: The Diels-Alder reaction – the endo rule - dawoodward-hoffman

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ChemTube3D 19.3: Diels–Alder reaction overview: The Diels-Alder reaction – the endo rule - daworking_out_which_product_is_endo

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ChemTube3D 21.4: Electrophilic addition to alkenes can produce stereoisomers

Electrophilic addition to alkenes can produce stereoisomers

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Chemistry³ 4e Student Resources eBook

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Step 1: Aldol reaction of cyclopentanone

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Step 1: Enolate reaction with bromine – bromination of ketone

First Bromination Step

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Step 2: Aldol reaction of cyclopentanone

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Step 2: Second Bromination Step – Base

Second Bromination Step

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Step 3: Aldol reaction of cyclopentanone

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Step 3: Third Bromination Step – Base

Third Bromination Step

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Step 4: Loss of the carbanion – Base

Loss of the carbanion

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Step 5: Formation of bromoform

Formation of bromoform

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Unstabilised Phosphonium Ylid Formation Wittig Reaction

Unstabilised Phosphonium Ylid Formation

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Wittig reaction – Ylid reaction with ketone

Ylid reaction with ketone

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Chapter 1 Self-test question

Fundamentals

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Chapter 2 Self-test question

The language of organic chemistry

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Chapter 3 Self-test question

Atomic structure and properties

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Chapter 4 Self-test question

Diatomic molecules

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Chapter 5 Self-test question

Polyatomic molecules

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Chapter 6 Self-test question

Solids

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Chapter 7 Self-test question

Acids and bases

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Chapter 8 Self-test question

Gases

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Chapter 9 Self-test question

Reaction kinetics

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Chapter 10 Self-test question

Molecular spectroscopy

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Chapter 11 Self-test question

Analytical chemistry

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Chapter 12 Self-test question

Molecular characterisation

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Chapter 13 Self-test question

Energy and thermochemistry

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Chapter 14 Self-test question

Entropy and Gibbs energy

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Chapter 15 Self-test question

Chemical equilibrium

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Chapter 16 Self-test question

Electrochemistry

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Chapter 17 Self-test question

Phase equilibrium and solutions

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Chapter 18 Self-test question

Isomerism and stereochemistry

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Chapter 19 Self-test question

Organic reaction mechanisms

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Chapter 20 Self-test question

Halogenoalkanes: substitution and elimination reactions

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Chapter 21 Self-test question

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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Chapter 22 Self-test question

Benzene and other aromatic compounds: electrophilic substitution reactions

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Chapter 23 Self-test question

Aldehydes and ketones: nucleophilic addition and α-substitution reactions

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Chapter 24 Self-test question

Carboxylic acids and derivatives: nucleophilic acyl substitution and α-substitution reactions

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Chapter 25 Self-test question

Hydrogen

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Chapter 26 Self-test question

s-Block chemistry

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Chapter 27 Self-test question

p-Block chemistry

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Chapter 28 Self-test question

d-Block chemistry

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ChemTube 3D 3.1 s, p, and d orbitals

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ChemTube 3D 4.1 H2 molecular orbitals

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ChemTube 3D 4.2 F₂ molecular orbitals

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HF molecular orbitals

ChemTube 3D 5.1 H2O, CH4, PF5, SF6, NH3, SF4, and ClF3

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ChemTube 3D 5.2 Methane (sp3) hybrid orbital

Methane (sp³) hybrid orbital

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ChemTube 3D 5.3 Ammonia (sp3) hybrid orbital

Ammonia (sp³) hybrid orbital

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ChemTube 3D 5.4 Ethene (sp2) hybrid orbital

Ethene (sp²) hybrid orbital

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ChemTube 3D 5.5 Ethyne (sp) hybrid orbital

Ethyne (sp) hybrid orbital

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ChemTube 3D 6.1 Diamond and graphite

Diamond and graphite

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ChemTube 3D 6.2 Cubic close packing

Cubic close packing – ccp

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ChemTube 3D 6.3 Body-centred cubic and primitive-cubic structures

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ChemTube 3D 6.4 Hexagonal close packing

Hexagonal close packing (hcp)

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ChemTube 3D 6.5 Structure of NaCl

Rocksalt (NaCl)

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ChemTube 3D 6.6 Structure of fluorite and anti-fluorite

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ChemTube 3D 6.7 Structure of NiAs

Nickel arsenide – NiAs

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ChemTube 3D 6.8 Structure of sphalerite and wurtzite

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ChemTube 3D 6.9 Structure of CdI2 and CdCl2

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ChemTube 3D 6.10 Structure of CsCl

CsCl – Caesium chloride

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ChemTube 3D 6.11 Structure of rutile

Structure of rutile

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ChemTube 3D 6.12 Structure of perovskite

Structure of perovskite

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ChemTube 3D 18.1: Conformations of ethane

Conformations of ethane

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ChemTube 3D 18.2: Newman projections for staggered and eclipsed conformations of butane

Newman projections for staggered and eclipsed conformations of butane

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ChemTube 3D 18.3: Conformations of butane

Conformations of butane

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ChemTube 3D 18.4: Chair and boat conformations of cyclohexane

Chair and boat conformations of cyclohexane

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ChemTube 3D 18.5: Assigning R or S configuration

Assigning R or S configuration

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ChemTube 3D 18.6: Diastereomers are stereoisomers that are not enantiomers

Isomerism and stereochemistry

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ChemTube 3D 18.7: Meso compounds

Meso compounds

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ChemTube 3D 19.1: Structures of methyl and tert-butyl cations

Structures of methyl and tert-butyl cations

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ChemTube3D 19.2: Nucleophilic addition to an α,β-unsaturated carbonyl

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ChemTube3D 19.3: Diels–Alder reaction overview

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ChemTube3D 20.1: SN2 reaction

S_N2 reaction

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ChemTube3D 20.2: SN1 reaction

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ChemTube3D 20.2: E2 reaction

E2 reaction

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ChemTube3D 20.3: E2 reaction of 2-bromobutane

E2 reaction of 2-bromobutane

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ChemTube3D 20.4: Stereospecific E2 reaction of 1-bromo-1,2-diphenylpropane

Stereospecific E2 reaction of 1-bromo-1,2-diphenylpropane

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ChemTube3D 20.5: E1 reaction

E1 reaction

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ChemTube3D 20.5: E1 reaction

Halogenoalkanes: substitution and elimination reactions

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ChemTube3D 20.6: Nucleophilic substitution reaction involving neighbouring group participation

Nucleophilic substitution reaction involving neighbouring group participation

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ChemTube3D 21.1: Electrophilic addition of HBr to an alkene

Electrophilic addition of HBr to an alkene

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ChemTube3D 21.2: Electrophilic addition of Br₂ to a symmetrical alkene

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ChemTube3D 21.3: Electrophilic addition of Br₂ to a asymmetrical alkene

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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ChemTube3D 21.4: Electrophilic addition of Br2 to cyclohexene

Electrophilic addition of Br₂ to cyclohexene

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ChemTube3D 21.5: Regioselective ring opening of an unsymmetrical bromonium ion

Regioselective ring opening of an unsymmetrical bromonium ion

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ChemTube3D 21.6: Hydroboration mechanism

Hydroboration mechanism

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ChemTube3D 21.7: Epoxidation of an alkene

Epoxidation of an alkene

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ChemTube3D 21.8: Periodate cleavage of 1,2-diols

Periodate cleavage of 1,2-diols

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ChemTube3D 21.9: Ozonolysis of an alkene

Ozonolysis of an alkene

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ChemTube3D 21.10: Suzuki reaction mechanism

Organopalladium Chemistry – The Suzuki Reaction

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ChemTube3D 22.1: Nitration of benzene

Nitration of benzene

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ChemTube3D 22.2: Sulfonation of benzene

Sulfonation of benzene

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ChemTube3D 22.3: Friedel–Crafts alkylation

Friedel–Crafts alkylation

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ChemTube3D 22.4: Friedel–Crafts acylation

Friedel–Crafts acylation

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ChemTube 3D 23.1: Borohydride reduction of an aldehyde

Borohydride reduction of an aldehyde

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ChemTube 3D 23.2: Formation of a cycanohydrin

Formation of a cycanohydrin

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ChemTube 3D 23.3: Organometallic nucleophilic addition to an aldehyde

Organometallic nucleophilic addition to an aldehyde

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Wittig reaction

ChemTube3D 23.5: Mechanism of formation of a hydrate

Mechanism of formation of a hydrate

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ChemTube3D 23.6: Formation of a hemiacetal

Formation of a hemiacetal

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ChemTube3D 23.7: Formation of an acetal

Formation of an acetal

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ChemTube3D 23.8: Formation of an imine

Formation of an imine

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ChemTube3D 23.9: Formation of an enamine

Formation of an enamine

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ChemTube3D 23.10: Acid-catalysed bromination of propanone

Acid-catalysed bromination of propanone

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ChemTube3D 23.11: Base-catalyzed enolization

Base-catalyzed enolization

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ChemTube3D 23.12: Base-catalysed bromination of propanone

Base-catalysed bromination of propanone

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Acid-catalysed aldol reaction

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ChemTube3D 23.14: Mechanism of an intramolecular aldol reaction

Mechanism of an intramolecular aldol reaction

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ChemTube3D 23.15: an animation of the nucleophilic addition of an organolithium and a Grignard reagent to an aldehyde?

Nucleophilic addition reactions of aldehydes and ketones

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ChemTube3D 24.1: Acid-catalysed esterification and ester hydrolysis

Acid-catalysed esterification and ester hydrolysis

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ChemTube3D 24.3: How pyridine acts as a catalyst in acylation reactions

Nucleophilic acyl substitution reactions

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ChemTube3D 24.4: Acid-catalysed hydrolysis of an ester

Acid-catalysed hydrolysis of an ester

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ChemTube3D 24.5: Claisen condensation of ethyl ethanoate

Claisen condensation of ethyl ethanoate

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ChemTube3D 25.1: Magnesium hydride

Magnesium hydride – MgH₂

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ChemTube3D 25.2: Structure of ice

Structure of ice

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ChemTube3D 28.1: Pt(NH₃)₂ coordinated to DNA

Pt(NH₃)₂ coordinated to DNA

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ChemTube3D 28.2: Metal–organic framework 5

MOF-5 (or IRMOF-1) Metal Organic Framework

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ChemTube3D 28.2: Structure of Prussian blue

Structure of Prussian blue

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Maths self-test questions

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Chapter 1 eBook

Fundamentals

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Chapter 2 eBook

The language of organic chemistry

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Chapter 3 eBook

Atomic structure and properties

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Chapter 4 eBook

Diatomic molecules

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Chapter 5 eBook

Polyatomic molecules

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Chapter 6 eBook

Solids

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Chapter 7 eBook

Acids and bases

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Chapter 8 eBook

Gases

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Chapter 9 eBook

Reaction kinetics

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Chapter 10 eBook

Molecular spectroscopy

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Chapter 11 eBook

Analytical chemistry

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Chapter 12 eBook

Molecular characterisation

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Chapter 13 eBook

Energy and thermochemistry

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Chapter 14 eBook

Entropy and Gibbs energy

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Chapter 15 eBook

Chemical equilibrium

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Chapter 16 eBook

Electrochemistry

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Chapter 17 eBook

Phase equilibrium and solutions

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Chapter 18 eBook

Isomerism and stereochemistry

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Chapter 19 eBook

Organic reaction mechanisms

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Chapter 20 eBook

Halogenoalkanes: substitution and elimination reactions

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Chapter 21 eBook

Alkenes and alkynes: electrophilic addition and pericyclic reactions

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Chapter 22 eBook

Benzene and other aromatic compounds: electrophilic substitution reactions

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Chapter 23 eBook

Aldehydes and ketones: nucleophilic addition and α-substitution reactions

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Chapter 24 eBook

Carboxylic acids and derivatives: nucleophilic acyl substitution and α-substitution reactions

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Chapter 25 eBook

Hydrogen

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Chapter 26 eBook

s-Block chemistry

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Chapter 27 eBook

p-Block chemistry

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Chapter 28 eBook

d-Block chemistry

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