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!
A structured KS5 lesson (Part 1 of 2) including starter activity, AfL work tasks and practice questions with answers on Group 2 Elements
By the end of this lesson KS5 students should be able to:
Know group 2 elements lose their outer shell s2 electrons to form +2 ions
State and explain the trend in first and second ionisation energies of group 2 elements and how this links to their relative reactivities with oxygen, water and dilute acids
Construct half equations of redox reactions of group 2 elements with oxygen, water and dilute acids and to identify what species have been oxidised and reduced using oxidation numbers
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
6 Full Lesson Bundle (includes a bonus lesson) on the topic of Equilibrium from the OCR A Level Chemistry specification plus an end of topic test. See below for the lessons and learning objectives
Lesson 1: Le Chatelier’s Principle
To explain the term dynamic equilibrium
To apply le Chatelier’s principle to homogeneous equilibria in order to deduce qualitatively the effect of a change in temperature, pressure or concentration on the position of equilibrium
To explain why catalysts do not change the position of equilibrium
To explain the importance to the chemical industry of a compromise between chemical equilibrium and reaction rate in deciding the operational conditions
Lesson 2: The Equilibrium Constant Kc (Part 1)
To construct expressions for the equilibrium constant Kc for homogeneous reactions
To calculate the equilibrium constant Kc from provided equilibrium concentrations
To estimate the position of equilibrium from the magnitude of Kc
To know the techniques and procedures used to investigate changes to the position of equilibrium for changes in concentration and temperature
Lesson 3: The Equilibrium Constant Kc (Part 2)
To construct expressions for the equilibrium constant Kc for homogeneous and heterogeneous reactions
To calculate units for Kc
To calculate quantities present at equilibrium and therefore kc given appropriate data
Lesson 4: Controlling The Position of Equilibrium (Kc)
To understand and explain the effect of temperature, concentration, pressure and catalysts on Kc and controlling the position of equilibrium
Lesson 5: The Equilibrium Constant Kp
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
Lesson 6 (BONUS): Chemical Equilibirum (Practical Skills):
To understand how a titration experiment can be used to calculate the equilibrium constant, Kc
To understand how a colorimeter can be used to calculate the equilibrium constant, Kc
To analyse exam questions based on titration experiments in order to calculate out Kc
End of Topic Test:
A 45 minute end of chapter test on chemical equilibrium. The test covers content from both year 12 and 13 OCR on chemical equilibrium. A markscheme with model answers is also included which enables students self assess their answers in class with their teacher or as a homework task.
The test is based on the following learning objectives:
Apply le Chatelier’s principle to deduce qualitatively (from appropriate information) the effect of a change in temperature, concentration or pressure, on a homogeneous system in equilibrium.
Explain that a catalyst increases the rate of both forward and reverse reactions in an equilibrium by the same amount resulting in an unchanged position of equilibrium
Deduce, for homogeneous and heterogeneous reactions, expressions for the equilibrium constant Kc.
Calculate the values of the equilibrium constant, Kc (from provided or calculated equilibrium moles or concentrations), including determination of units.
Estimate the position of equilibrium from the magnitude of Kc.
Calculate, given appropriate data, the concentration or quantities present at equilibrium.
Deduce, for homogeneous and heterogeneous reactions, expressions for the equilibrium constant Kp.
Calculate the values of the equilibrium constant, Kp (from provided or calculated equilibrium moles or pressures), including determination of units.
Explain the effect of changing temperature on the value of Kc or Kp for exothermic and endothermic reactions.
State that the value of Kc or Kp is unaffected by changes in concentration or pressure or by the presence of a catalyst.
Explain how Kc or Kp controls the position of equilibrium on changing concentration, pressure and temperature
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 proton NMR Spectroscopy (part 2)
NOTE: This lesson can be purchased as a bundle with proton NMR Spectroscopy (part 1)
By the end of this lesson KS5 students should be able to:
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
2 Bonus Questions on Combined Techniques are also included in this 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
17 well structured chemistry lessons plus a BONUS revision summary covering topics in Module 6 of the OCR Specification: **Organic Chemistry **
*Note: Lessons on Analysis: chromatography, qualitative analysis of functional groups and NMR spectroscopy are sold as a separate bundle in my shop) *
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
To state the IUPAC name of substituted aromatic compounds
Construct the structure of aromatic compounds based on their IUPAC names
To 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
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
Lesson 6: Reactions of Carbonyl Compounds
To understand the oxidation of aldehydes using Cr2O72-/H+ to form carboxylic acids
To understand nucleophilic addition reactions of carbonyl compounds with:
NaBH4 to form alcohols
HCN (NaCN (aq)/H+ (aq)) to form hydroxynitriles
To construct the mechanism for nucleophilic addition reactions of aldehydes and ketones with NaBH4 and HCN
Lesson 7: Testing for Carbonyl Compounds
To understand the use of Tollens’ reagent to:
(i) detect the presence of an aldehyde group
(ii) distinguish between aldehydes and ketones, explained in terms of the oxidation of aldehydes to carboxylic acids with reduction of silver ions to silver
To understand the use of 2,4-dinitrophenylhydrazine to:
(i) detect the presence of a carbonyl group in an organic compound
(ii) identify a carbonyl compound from the melting point of the derivative
Lesson 8: Carboxylic acids and Esters
To explain the water solubility of carboxylic acids in terms of hydrogen bonding
To recall the reactions in aqueous conditions of carboxylic acids with metals and bases (including carbonates, metal oxides and alkalis)
To know the esterification of: (i) carboxylic acids with alcohols in the presence of an acid catalyst (ii) acid anhydrides with alcohols
To know the hydrolysis of esters: (i) in hot aqueous acid to form carboxylic acids and alcohols (ii) in hot aqueous alkali to form carboxylate salts and alcohols
Lesson 9: Acyl Chlorides and Their Reactions
To know how to name acyl chlorides
To recall the equation for the formation of acyl chlorides from carboxylic acids using SOCl2
To construct equations for the use of acyl chlorides in the synthesis of esters, carboxylic acids and primary and secondary amides
Lesson 10: Introduction to Amines
To know how to name amines using IUPAC rules
To understand the basicity of amines in terms of proton acceptance by the nitrogen lone pair
To understand the reactions of amines with dilute inorganic acids
Lesson 11: Preparation of Amines
To know the reaction steps involved in the preparation of aromatic amines by reduction of nitroarenes using tin and concentrated hydrochloric acid
To know the reaction steps involved in the preparation of aliphatic amines by substitution of haloalkanes with excess ethanolic ammonia or amines
To explain the reaction conditions that favours the formation of a primary aliphatic amine
To explain the reaction conditions that favours the formation of a quaternary ammonium salt
Lesson 12: Amino Acids and Their Reactions
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
Lesson 13: Chirality
To know that optical isomerism is an example of stereoisomerism, in terms of non- superimposable mirror images about a chiral centre
To identify chiral centres in a molecule of any organic compound.
To construct 3D diagrams of optical isomers including organic compounds and transition metal complexes
Lesson 14: Amides
To review the synthesis of primary and secondary amides
To understand the structures of primary and secondary amides
To name primary and secondary amides
Lesson 15: Condensation Polymers
To know that condensation polymerisation can lead to the formation of i) polyesters ii) polyamides
To predict from addition and condensation polymerisation:
i) the repeat unit from a given monomer(s)
(ii) the monomer(s) required for a given section of a polymer molecule
(iii) the type of polymerisation
To understand the acid and base hydrolysis of i) the ester groups in polyesters ii) the amide groups in polyamides
Lesson 16: Practical Skills in Organic Synthesis (Yr13)
To describe the techniques and procedures used for the purification of organic solids including:
filtration under reduced pressure
recrystallisation
measurement of melting points
Lesson 17: Synthetic Routes in Organic Synthesis (Y13)
To identify individual functional groups for an organic molecule containing several functional groups
To predict the properties and reactions of organic molecules containing several functional groups
To create multi-stage synthetic routes for preparing organic compounds
Synthetic Routes Revision Summary
A 14 page summary of all the organic synthesis reactions from the AS and A level OCR 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* electrophilic substitution reactions* reactions of phenols* carbon-carbon formation reactions* reactions of carboxylic acids* reactions of acyl chlorides* polymerisation reactions* hydrolysis reactions* amine synthesis reactions*
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
5 well structured chemistry lessons covering topics in the Introduction to Organic Chemistry (Year 12) suitable for the AQA specification (IMPORTANT NOTE: please look in my shop for similar bundle suitable for the OCR specification)
Lesson 1: Organic and Inorganic Compounds
Describe what organic and inorganic compounds are
Compare the strength of bonds in organic and inorganic compounds
Explain the molecular shape of carbon containing compounds
Lesson 2: Naming organic compounds
By the end of the lesson students should be able to:
Know the IUPAC rules for naming alkanes and alkenes
Know the IUPAC rules for naming aldehyde, ketones and carboxylic acids
Construct structural or displayed formulae from named organic compounds and name organic compounds from the structural or displayed formulae
Lesson 3: Types of formulae
By the end of the lesson students should be able to:
Know what is meant by the terms empirical and molecular formula
Compare the terms general, structural, displayed and skeletal formula
Construct organic compounds using either of the 6 types of formulae
Lesson 4: Isomers
Know the what structural isomers and stereoisomers are
Describe the three different ways in which structural isomers can occur
Construct formulae of positional, functional group or chain isomers and stereosiomers of alkenes
Lesson 5: Introduction To Reaction Mechanisms
Understand that reaction mechanisms are diagrams that illustrate the movement of electrons using curly arrows
Understand where curly arrows being and where they end
Identify and illustrate homolytic and heterolytic bond fission in reaction mechanisms
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 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
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 Periodicity: Melting Points
By the end of this lesson KS5 students should be able to:
To describe the trend in structure from giant metallic to giant covalent to simple molecular lattice
To explain the variation in melting points across period 2 & 3 in terms of structure and 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 reviewed during these scenarios outlined above
A complete lesson including starter activity, AfL work tasks and main work tasks (all with answers included) on The Preparation of Amines
By the end of this lesson KS5 students should be able to:
To know the reaction steps involved in the preparation of aromatic amines by reduction of nitroarenes using tin and concentrated hydrochloric acid
To know the reaction steps involved in the preparation of aliphatic amines by substitution of haloalkanes with excess ethanolic ammonia or amines
To explain the reaction conditions that favours the formation of a primary aliphatic amine
To explain the reaction conditions that favours the formation of a quaternary ammonium salt
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 lesson including starter activity, AfL activities and main work task with answers on pH and neutralisation. Suitable for AQA GCSE Chemistry and higher tier combined science
Then by the end of this lesson KS4 students should be able to:
To state the ionic equation involved in neutralisation reactions
To describe the use of a universal indicator to measure pH changes
To compare acid strength and concentration
The teacher will be able to check students have met these learning objectives through mini AfL tasks and main work tasks for students to complete
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
Well structured KS5 Lesson on Benzene and its structure. The lesson contains starter activities, discussion questions and mini AfL quizzes and practice questions, all with answers included
By the end of the lesson students should:
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
4.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
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 well structured KS5 Lesson on Directing Groups in Aromatic Compounds. This lesson is a follow up to the lesson on Phenols. This lesson contains a starter activity, mini AfL questions and practice questions, all with answers included
By the end of the lesson students should:
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
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
11 Full Lesson Bundle covering the OCR A Level Chemistry Chapter on Electrons, Bonding & Structure. Lessons are also suitable for AQA and Edexcel (please review the learning objectives below).
**Lesson 1: Atomic Orbitals
To know that atomic orbitals are a region around the nucleus that occupy electrons
To illustrate the shape of s, p and d orbitals
To describe the number of orbitals that make up the s, p and d sub shells and the number of electrons that fill the sub shells
To deduce the electronic configuration of atoms and ions in the s and p-block
**Lesson 2: Electronic Configuration of d-block elements
To recall the order of electron shells to be filled
To construct electronic configurations of d-block atoms and ions
To know the elemental anomalies in electron filling of d block atoms
**Lesson 3: Ionic Bonding
To know ionic bonding as electrostatic attraction between positive and negative ions, and the construction of ‘dot-and-cross’ diagrams
To explain solid structures of giant ionic lattices are a result of oppositely charged ions strongly attracted to each other in all directions
To link the structure and bonding of ionic compounds on their physical properties including melting and boiling points, solubility and electrical conductivity in solid, liquid and aqueous states
**Lesson 4: Covalent and Dative Covalent Bonding
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
**Lesson 5: Simple and Giant Covalent Structures
To describe the structure of simple and giant covalent compounds
To explain how the structure and bonding of simple and giant covalent compounds link to their different physical properties
To evaluate the potential applications of covalent structures based on their physical properties (stretch & challenge)
**Lesson 6: Metallic Bonding and Structure
To describe the structure of metals
To explain metallic bonding as strong electrostatic attraction between cations and delocalised electrons
To explain the physical properties of giant metallic structures
**Lesson 7: Shapes of Molecules and Ions
To determine the number of bonding pairs & lone pairs in a molecule or ion
To recall the shapes and bond angles of molecules and ions with up to six electron pairs surrounding the central atom
To 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
**Lesson 8: Electronegativity and Bond Polarity
To define the term electronegativity
To explain the trend in electronegativity down a group and across a period
To explain what a polar covalent bond is bond and to illustrate this type of bond in a molecule
**Lesson 9: Polar and Non-Polar Molecules
To describe the difference between polar and non-polar molecules
To explain why non-polar molecules can contain polar bonds
To predict whether molecules are polar or non-polar
**Lesson 10 : Intermolecular Forces (Part 1)
Understand intermolecular forces based on induced-dipole interactions and permanent dipole-dipole interactions
Explain how intermolecular forces are linked to physical properties such as boiling and melting points
Compare the solubility of polar and non-polar molecules in polar and non-polar solvents
**Lesson 11 : Intermolecular Forces (Part 2)
To understand hydrogen bonding as intermolecular forces between molecules containing N, O or F and the H atom of –NH, -OH or HF
To construct diagrams which illustrate hydrogen bonding
To explain the anomalous properties of H2O resulting from hydrogen 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 reviewed during these scenarios outlined above
A structured KS5 lesson including starter activity, AfL work tasks and lesson slides on the properties of alkenes. This lesson is an introduction to the chapter on alkenes. This lesson follows the OCR specification.
By the end of the lessons students should be able:
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**
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 practice questions with answers on Gibbs Free Energy (Part 2)
By the end of this lesson KS5 students should be able:
To state and use the relationship ΔG = ΔH-TΔS
To draw a link between ΔG and feasibility
To explain the limitations of predictions made by ΔG about feasibility, in terms of kinetics.
The teacher will be able to check students have met these learning objectives through mini AfL tasks for students to complete
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 (Yr12) including starter activity, discussion questions, videos and main work task all with answers included on Practical Skills for Organic Synthesis. Suitable for the OCR specification.
By the end of this lesson KS5 students should be able to:
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:
use of a separating funnel to remove an organic layer from an aqueous layer
drying with an anhydrous salt
redistillation
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 and AfL work tasks and main work tasks and plenary quiz on Transition Metals & Their Compounds. All answers included
**By the end of this lesson KS5 students should be able to:
To know the electron configuration of atoms and ions of the d-block elements of Period 4 (Sc–Zn), given the atomic number and charge
2.To understand the elements Ti–Cu as transition elements
To illustrate, using at least two transition elements, of:
(i) the existence of more than one oxidation state for each element in its compounds
(ii) the formation of coloured ions
(iii) the catalytic behaviour of the elements and their compounds and their importance in the manufacture of chemicals by industry
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
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 12 KS5 lesson including starter activity and AfL work tasks on The Boltzmann Distribution. Suitable for OCR Specification (AS Chemistry)
By the end of this lesson KS5 students should be able to:
**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 structured KS5 lesson including starter activity, AfL work tasks and main work task all with answers on Buffer Solution Calculations (Suitable for the OCR Specification)
By the end of this lesson KS5 students should be able to:
To calculate the pH of a buffer solution containing a weak acid and the salt of a weak acid by using the Ka expression and pH equation
To calculate equilibrium concentrations, moles or mass of the components of a weak acid-salt of a weak acid buffer solution
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, mini AfL work tasks with answers, main work tasks with answers for a KS5 lesson on isomers (structural isomers and stereoisomers). Suitable for the AQA specification
By the end of the lesson students should be able to:
Know the what structural isomers and stereoisomers are
Describe the three different ways in which structural isomers can occur
Construct formulae of positional, functional group or chain isomers and stereosiomers of alkenes
Students will be able to take rich notes on isomers, building on their KS4 knowledge on this topic
The teacher will be able to quickly assess students’ understanding on isomers by carrying our mini AfL tasks either on mini white boards or in students’ books
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, risk assessment and post practical plenary questions on Chemistry Required Practical :Preparing a pure, dry sample of a soluble salt from an insoluble oxide or carbonate
Lesson includes lab report for students to fill in
By the end of this lesson KS4 students should be able to:
→ Describe a practical procedure for producing a salt from a solid and an acid
→ Explain the apparatus, materials and techniques used for making the salt
→ Describe how to safely manipulate apparatus and accurately measure melting points
This lesson should be taught as a practical 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 assessed during the scenarios outlined above