Over 200 resources available for KS3-KS4 Science, KS5 Chemistry and Whole School! Lesson resources are suitable for live lessons in school, remote teaching at home or independent student study. It’s your choice how you use them 😊 Don’t forgot to explore my free resources too!
Over 200 resources available for KS3-KS4 Science, KS5 Chemistry and Whole School! Lesson resources are suitable for live lessons in school, remote teaching at home or independent student study. It’s your choice how you use them 😊 Don’t forgot to explore my free resources too!
3 Full Lesson Bundle which covers the Kinetics chapter from the OCR AS Level Chemistry Specification (may also suitable for the AQA and Edexcel Spec- see Learning Objectives below to confirm)
Lesson 1: Collision Theory & Rates of Reaction
**1. To explain the effect of concentration (including pressure of gases only) on the rate of reaction in terms of the frequency of collisions
**2. To calculate the rate of reaction using the gradients of a concentration-time graph
**3. To describe the techniques and procedures used to investigate reaction rates including the measurement of mass, gas volumes and concentration
Lesson 2: Catalysts
**1. To explain the effect of concentration (including pressure of gases only) on the rate of reaction in terms of the frequency of collisions
**2. To calculate the rate of reaction using the gradients of a concentration-time graph
**3. To describe the techniques and procedures used to investigate reaction rates including the measurement of mass, gas volumes and concentration
Lesson 3: The Boltzmann Distribution
**1. To draw a labelled diagram of the Boltzmann distribution
**2. To explain qualitatively the Boltzmann distribution and its relationship with activation energy
**3. To explain how temperature changes and catalytic behaviour effect the proportion of molecules exceeding the activation energy and hence the reaction rate using Boltzmann distributions
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons including using your own lesson PowerPoints is a fundamental skill of a qualified/unqualified teacher that will be reviewed during these scenarios outlined above
A well structured KS5 Lesson on Phenols. The lesson contains a starter activity, mini AfL questions and practice questions, all with answers included
By the end of the lesson students should:
To recall and explain the electrophilic substitution reactions of phenol:
with bromine to form 2,4,6-tribromophenol
(ii) with dilute nitric acid to form a mixture of 2-nitrophenol and 4-nitrophenol
(j) To explain the relative ease of electrophilic substitution of phenol compared with benzene, in terms of electron pair donation to the π-system from an oxygen p-orbital in phenol
To understand the weak acidity of phenols shown by its neutralisation reaction with NaOH but absence of reaction with carbonates
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons,including using your own lesson PowerPoints, is a fundamental skill of a qualified/unqualified teacher that will be assessed during the scenarios outlined above
5 Full Lesson Bundle on Analysis from the OCR A Level Chemistry specification. Please review the learning objectives below.
Lesson 1: Chromatography
To interpret one-way TLC chromatograms in terms of Rf values
To interpret gas chromatograms in terms of:
(i) retention times
(ii) the amounts and proportions of the components in a mixture
To understand the creation and use of external calibration curves to confirm concentrations of components.
Lesson 2: Qualitative Analysis of Organic Functional Groups
To recall qualitative analysis of organic functional groups on a test-tube scale
To design qualitative analysis tests to distinguish between two or more organic compounds
Lesson 3: Carbon-13 NMR Spectroscopy
To analyse a carbon-13 NMR spectrum of an organic molecule to make predictions about:
The number of carbon environments in the molecule
The different types of carbon environment present from chemical shift values
Possible structures for the molecule
Lesson 4: Proton NMR Spectroscopy (Part 1)
To analyse proton NMR spectra of an organic molecule to make predictions about:
The number of proton environments in the molecule
The different types of proton environment present from chemical shift values
Lesson 5: Proton NMR Spectroscopy (Part 2) (includes combined techniques)
To analyse proton NMR spectra of an organic molecule to make predictions about:
The different types of proton environment present from chemical shift values
The relative numbers of each type of proton present from the relative peak areas using integration traces or ratio numbers when required
The number of non-equivalent protons adjacent to a given proton from the spin-spin splitting pattern, using the n+1 rule
Possible structures for the molecule
Note: 2 Exam Questions on Combined Techniques are also included in lesson 5!
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A structured KS5 lesson including starter activity, AfL work tasks and main work task all with answers on the shapes of molecules and ions
By the end of this lesson KS5 students should be able to:
Determine the number of bonding pairs & lone pairs in a molecule or ion
Recall the shapes and bond angles of molecules and ions with up to six electron pairs surrounding the central atom
Explain the shapes of molecules and ions using the electron pair repulsion theory
To construct diagrams to illustrate the 3D shapes of molecules and ions
**Note: If molecular modeling kits are not available then step 3 from the discovery task can simply be deleted from slide 6.
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons including using your own lesson PowerPoints is a fundamental skill of a qualified/unqualified teacher that will be reviewed during these scenarios outlined above
A structured Year 13 KS5 lesson ( lesson 2 of 2) on Concentration-Time Graphs. Lesson includes starter activity, worked examples and Afl quiz
By the end of this lesson KS5 students should be able to:
To deduce zero & first order reactants from concentration-time graphs
To calculate the rate constant of a first order reactant using their half-life
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons, including using your own lesson PowerPoints, is a fundamental skill of a qualified/unqualified teacher that will be assessed during the scenarios outlined above
A complete A Level Chemistry KS5 lesson including starter activity, main work task and answers on acid-base titration calculations
By the end of this lesson KS5 students should be able to:
To apply mole calculations to complete structured titration calculations, based on experimental results of familiar acids and bases.
To apply mole calculations to complete non-structured titration calculations, based on experimental results of non-familiar acids and bases
All tasks have worked out answers which will allow students to self assess their work in the lesson
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons including using your own lesson PowerPoints is a fundamental skill of a qualified/unqualified teacher that will be reviewed during these scenarios outlined above
A structured KS5 lesson including starter activity, AfL work tasks and main work task all with answers on Mass Spectrometry in Organic Chemistry. Suitable for OCR AS Chemistry.
By the end of the lesson, students should be able to:
Use a mass spectrum of an organic compound to identify the molecular ion peak and hence to determine molecular mass
2)Perform analysis of fragmentation peaks in a mass spectrum to identify parts of structures
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A structured KS5 lesson including starter activity, AfL work tasks and main work task all with answers on Mass Spectroscopy. Suitable for OCR AS Chemistry
By the end of this lesson KS5 students should be able to:
To determine the relative atomic masses and relative abundances of the isotope using mass spectroscopy
To calculate the relative atomic mass of an element from the relative abundances of its isotope
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons, including using your own lesson PowerPoints, is a fundamental skill of a qualified/unqualified teacher that will be assessed during the scenarios outlined above
A complete lesson including starter activity, mini AfL work tasks with answers, main work tasks with answers for a KS5 lesson on moles and volumes (solutions and gas volumes)
By the end of the lesson students should be able to:
To calculate the amount of substance in mol, involving solution volume and concentration
To understand the terms dilute, concentrated and molar
To explain and use the term molar gas volume
To calculate the amount of substance in mol, involving gas volume
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A complete lesson including starter activity, AfL work tasks and main work tasks (all with answers included) on Amino Acids And Their Reactions
By the end of this lesson KS5 students should be able to:
To know the general formula for an α-amino acid as RCH(NH2)COOH
To understand the following reactions of amino acids:
(i) reaction of the carboxylic acid group with alkalis and in the formation of esters
(ii) reaction of the amine group with acids
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons including using your own lesson PowerPoints is a fundamental skill of a qualified/unqualified teacher that will be reviewed during these scenarios outlined above
A complete lesson including starter activity, AfL work tasks and main work tasks (all with answers included) on Amides
By the end of this lesson KS5 students should be able to:
To review the synthesis of primary and secondary amides
To understand the structures of primary and secondary amides
To name primary and secondary amides
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons including using your own lesson PowerPoints is a fundamental skill of a qualified/unqualified teacher that will be reviewed during these scenarios outlined above
A whole lesson including starter activity, AfL work tasks and main work task all with answers on Internal Energy
By the end of this lesson KS4 students should be able to:
Describe the particle model of matter
Understand what is meant by the internal energy of a system
Describe the effect of heating on the energy stored within a system
The teacher will be able to check students have met these learning objectives through mini AfL tasks for students to complete
All tasks have worked out answers, which will allow students to self assess their work during the lesson
5 Full Lesson Bundle which covers the lessons on aromatic compounds from the OCR A Level Chemistry Specification. See below for the lesson objectives
Lesson 1: Benzene and its Structure
To describe the Kekulé model of benzene
To describe the delocalised model of benzene in terms of P orbital overlap forming a delocalised π system
To compare the Kekulé model of benzene and the delocalised model of benzene
To explain the experimental evidence which supports the delocalised model of benzene in terms of bond lengths, enthalpy change of hydrogenation and resistance to reaction
Lesson 2: Naming Aromatic Compounds
State the IUPAC name of substituted aromatic compounds
Construct the structure of aromatic compounds based on their IUPAC names
Analyse the correct numbering system for di and trisubstituted aromatic compounds
Lesson 3: The Reactions of Benzene
To understand the electrophilic substitution of aromatic compounds with:
(i) concentrated nitric acid in the presence of concentrated sulfuric acid
(ii) a halogen in the presence of a halogen carrier
(iii) a haloalkane or acyl chloride in the presence of a halogen carrier (Friedel–Crafts reaction) and its importance to synthesis by formation of a C–C bond to an aromatic ring
To construct the mechanism of electrophilic substitution in arenes
Lesson 4: Phenols
To recall and explain the electrophilic substitution reactions of phenol:
with bromine to form 2,4,6-tribromophenol
(ii) with dilute nitric acid to form a mixture of 2-nitrophenol and 4-nitrophenol
(j) To explain the relative ease of electrophilic substitution of phenol compared with benzene, in terms of electron pair donation to the π-system from an oxygen p-orbital in phenol
To understand the weak acidity of phenols shown by its neutralisation reaction with NaOH but absence of reaction with carbonates
Lesson 5: Directing Groups in Aromatic Compounds
To understand the 2- and 4-directing effect of electron- donating groups (OH, NH2) and the 3-directing effect of electron-withdrawing groups (NO2) in electrophilic substitution of aromatic compounds
To predict the substitution products of aromatic compounds by directing effects in organic synthesis
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A structured KS5 lesson including starter activity, AfL work tasks, main work tasks with answers on The Equilibrium Constant Kp
By the end of the lesson students should be able to:
To use the terms mole fraction and partial pressure
To construct expressions for Kp for homogeneous and heterogeneous equilibria
To calculate Kp including determination of units
To understand the affect of temperature, pressure, concentration and catalysts on Kp and controlling the position of equilibrium
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A 16 page pdf summary of all the organic synthesis reactions from the AS and A level AQA Chemistry specification. Students will be able to use this resource directly as part of their revision on organic synthesis/synthetic routes or can make flashcards from them. Reagents and reaction conditions are also included where applicable
Reaction summaries include:
nucelophilic substitution reactions* elimination reactions* free radical substitution reactions* electrophilic addition reactions* oxidation reactions* reduction reactions* ethanol production reactions* electrophilic substitution reactions* nucleophilic addition reactions* nucleophilic addition-elimination reactions* carbon-carbon bond formation reactions* reactions of carboxylic acids* reactions of acyl chlorides* reactions of acid anhydrides* polymerisation reactions* hydrolysis reactions* amine synthesis reactions* Biodiesel formation reactions* Transesterification reactions*
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20 well structured chemistry lessons covering topics in Module 4 of the OCR Specification: **Core Organic Chemistry **
*(Note: Lessons on Analytical techniques: IR and Mass spectroscopy are sold as a separate bundle in my shop) *
Lesson 1: Organic and Inorganic Compounds
To describe what organic and inorganic compounds are
2 To compare the strength of bonds in organic and inorganic compounds
To explain the molecular shape of carbon containing compounds
Lesson 2: Naming organic compounds
To know the IUPAC rules for naming alkanes and alkenes
To know the IUPAC rules for naming aldehyde, ketones and carboxylic acids
To construct structural or displayed formulae from named organic compounds and name organic compounds from the structural or displayed formulae
Lesson 3: Types of formulae
To know what is meant by the terms empirical and molecular formula
To compare the terms general, structural, displayed and skeletal formula
To construct organic compounds using either of the 6 types of formulae
Lesson 4: Isomers
To describe what structural isomers and stereoisomers are
To construct formulae of structural isomers of various compounds
To construct formulae of E-Z and cis-trans stereoisomers of alkenes
Lesson 5: Introduction To Reaction Mechanisms
To understand that reaction mechanisms are diagrams that illustrate the movement of electrons using curly arrows
To understand where curly arrows being and where they end
To identify and illustrate homolytic and heterolytic bond fission in reaction mechanisms
Lesson 6: Properties of Alkanes
To know alkanes are saturated alkanes containing sigma (σ)bonds that are free to rotate
To explain the shape and bond angle round each carbon atom in alkanes in terms of electron pair repulsion
To describe and explain the variations in boiling points of alkanes with different carbon chain lengths and branching in terms of London forces
Lesson 7: Combustion of Alkanes
To understand why alkanes are good fuels
To recall the equations (both word and symbol) for complete combustion of alkanes
To recall the equations (both word and symbol) for incomplete complete combustion of alkanes
Lesson 8: Free Radical Substitution of Alkanes
To know what a free radical is
To describe the reaction mechanism for the free-radical substitution of alkanes including initiation, propagation and termination
To analyse the limitations of radical substitution in synthesis by formation of a mixture of organic products
Lesson 9: The Properties of Alkenes
1.To know the general formula of alkenes
2. To explain the shape and bond angle around each carbon atom of a C=C bond
3. To describe how π and σ bonds are formed in alkenes
Lesson 10: Addition Reactions of Alkenes
To know what an electrophile is
To describe what an electrophilic addition reaction is
To outline the mechanism for electrophilic addition
Lesson 11: Addition Polymerisation
To know the repeat unit of an addition polymer deduced from a polymer
To identify the monomer that would produce a given section of an addition polymer
To construct repeating units based on provided monomers
Lesson 12: Dealing with Polymer Waste
To understand the benefits for sustainability of processing waste polymers by:
Combustion for energy production
Use as an organic feedstock for the production of plastics and other organic chemicals
Removal of toxic waste products such as HCl
To understand the benefits to the environment of development of biodegradable and photodegradable polymers
Lesson 13: Properties of Alcohols
To identify and explain the intermolecular forces that are present in alcohol molecules
To explain the water solubility of alcohols, their low volatility and their trend in boiling points
To classify alcohols as primary, secondary or tertiary alcohols
Lesson 14: Oxidation of Alcohols
To know that alcohols can undergo combustion reactions in the presence of oxygen
To know alcohols can be oxidised by an oxidising agent called acidified potassium dichromate
To know the products and reaction conditions for the oxidation of primary alcohols to aldehydes and carboxylic acids
To know the products and reaction conditions for the oxidation of secondary alcohols to ketones
Lesson 15: Other Reactions of Alcohols
To know the elimination of H2O from alcohols in the presence of an acid catalyst and heat to form alkenes
To know the substitution of alcohols with halide ions in the presence of acid to form haloalkanes
Lesson 16: Haloalkanes and their Reactions (part 1)
To define and use the term nucleophile
To outline the mechanism for nucleophilic substitution of haloalkanes
Lesson 17: Haloalkanes and their Reactions (part 2)
To explain the trend in the rates of hydrolysis of primary haloalkanes in terms of the bond enthalpies of carbon-halogen bonds
To describe how the rate of hydrolysis of haloalkanes can be determined by experiment using water, ethanol and silver nitrate solution
Lesson 18: Haloalkanes and the environment
To know how halogen radicals are produced from chlorofluorocarbons (CFCs) by the action of UV radiation
To construct equations for the production of halogen radicals from CFCs
To construct equations for the catalysed breakdown of ozone by Cl. and other radicals (NO.)
Lesson 19: Practical skills for organic synthesis
To demonstrate knowledge, understanding and application of the use of Quickfit apparatus for distillation and heating under reflux
To understand the techniques for preparation and purification of an organic liquid including:
Lesson 20: Synthetic routes in organic synthesis
To identify individual functional groups for an organic molecule containing several functional groups
To predict the properties and reactions of an organic molecule containing several functional groups
To create two-stage synthetic routes for preparing organic compounds
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A structured KS5 lesson including starter activity, AfL work tasks and main work task all with answers on the acid dissociation constant Ka
By the end of this lesson KS5 students should be able to:
To understand the acid dissociation constant, Ka, as the extent of acid dissociation
To know the relationship between Ka and pKa
To convert between Ka and pKa
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons, including using your own lesson PowerPoints, is a fundamental skill of a qualified/unqualified teacher that will be assessed during the scenarios outlined above
A structured KS5 lesson including starter activity, AfL work tasks and plenary task all with answers on Neutralisation & Titration Curves
By the end of this lesson KS5 students should be able to:
To interpret titration curves of strong and weak acids and strong and weak bases
To construct titration curve diagrams of strong and weak acids and strong and weak bases
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons, including using your own lesson PowerPoints, is a fundamental skill of a qualified/unqualified teacher that will be assessed during the scenarios outlined above
A structured KS5 lesson including starter activity, AfL work tasks and main work task all with answers on the pH of weak acids
By the end of this lesson KS5 students should be able to:
To recall the expression of pH for weak monobasic acids
To calculate the pH of weak monobasic acids using approximations
To analyse the limitations of using approximations to Ka related calculations for ‘stronger’ weak acids
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons, including using your own lesson PowerPoints, is a fundamental skill of a qualified/unqualified teacher that will be assessed during the scenarios outlined above
A structured KS5 lesson including starter activity, AfL work tasks and main work task all with answers on Covalent and Dative Covalent Bonding
By the end of this lesson KS5 students should be able:
To know covalent bonding as electrostatic attraction between a shared pair of electrons and the nucleus
To construct dot and cross diagrams of molecules and ions to describe single and multiple covalent bonding
To apply the term average bond enthalpy as a measurement of covalent bond strength
To know what a dative covalent bond is
To construct dot and cross diagrams of molecules and ions to describe dative covalent bonding
Declaimer: Please refrain from purchasing this popular resource for an interview lesson or a formal observation. This is because planning your own lessons, including using your own lesson PowerPoints, is a fundamental skill of a qualified/unqualified teacher that will be assessed during the scenarios outlined above
