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

15 Full Lesson Bundle (included a free bonus lesson) covering the module 2.1 on Atoms & Reactions from the OCR A Level Chemistry A Specification. See below for the lesson objectives. Lesson 1: Atomic Structure & Isotopes To describe the atomic structure of an atom To describe atomic structure in terms of protons, neutrons and electrons for atoms and ions, given the atomic number, mass number and any ionic charge To define the term isotopes and to identify the atomic structure of isotopes in terms of protons, neutrons and electrons Lesson 2: Relative Masses To define the terms relative atomic mass, relative formula mass and relative molecular mass To calculate the relative formula mass and relative molecular mass of compounds and molecules Lesson 3: Mass Spectroscopy 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 Lesson 4: Ions & The Periodic Table To predict the ionic charge of ions based on the position of the element in the periodic table To recall the names of common atomic and molecular ions To be able write the formula of ionic compounds Lesson 5: Empirical and Molecular Formulae To understand what is meant by ‘empirical formula’ and ‘molecular formula’ To calculate empirical formula from data giving composition by mass or percentage by mass To calculate molecular formula from the empirical formula and relative molecular mass. **Lesson 6: Water of Crystallisation ** To know the terms anhydrous, hydrated and water of crystallisation To calculate the formula of a hydrated salt from given percentage composition or mass composition To calculate the formula of a hydrated salt from experimental results Lesson 7: Moles & Volumes (Solutions & Gas Volumes) 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 Lesson 8: Moles & Equations To know how to balance symbol equations To calculate the moles of reactants or products based on chemical equations and mole ratios To calculate the masses of reactants used or products formed based on chemical equations and mole ratios Lesson 9: Percentage Yield and Atom Economy To know how to balance symbol equations To calculate atom economy and percentage yield from balanced symbol equations To calculate the masses and moles of products or reactants from balanced symbol equations Lesson 10: Acids, Bases & Neutralisation To know the formula of common acids and alkalis To explain the action of an acid and alkali in aqueous solution and the action of a strong and weak acid in terms of relative dissociations To describe neutralisation as a reaction of: (i) H+ and OH– to form H2O (ii) acids with bases, including carbonates, metal oxides and alkalis (water-soluble bases), to form salts, including full equations Lesson 11: Acid-Base Titration Procedures To outline the techniques and procedures used when preparing a standard solution of required concentration To outline the techniques and procedures used when carrying out acid–base titrations To determine the uncertainty of measurements made during a titration practical Lesson 12: Acid-Base Titration Calculations 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 Lesson 13: Oxidation States To recall the rules for oxidation states of uncombined elements and elements in compounds To determine the oxidation states of elements in a redox reaction To identify what substance has been reduced or oxidised in a redox reaction Lesson 14: Half Equations (Redox Reactions) To understand what a half equation is To explain what a redox equation is To construct half equations from redox equations Lesson 15: Redox Equations To identify what substance has been reduced or oxidised in a redox reaction To construct balanced half equations by adding H+ and H2O To construct full ionic redox equations from half equations **Note: Lesson 15 is a free bonus (stretch & challenge) lesson that focuses on redox in year 13 (module 5.2.3 (spec points a-c)) ** 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

8 Full Lesson Bundle which covers the redox and electrode potential section of the OCR Energy Chapter: Lesson 1 & 2: Redox Reactions Lesson 3& 4: Redox Titrations Lesson 5&6: Standard Electrode & Cell Potentials Lesson 7: Limitations of Cell Potentials Lesson 8: Storage & Fuel Cells Learning Objectives: Lesson 1: LO1: To identify the oxidation numbers of elements in ions and compounds LO2: To construct half-equations from redox equations LO3: To explain and use the terms oxidising agent and reducing agent Lesson 2: LO1: To understand that the overall increase in oxidation number will equal the overall decrease in oxidation number LO2: To construct balanced half equations and overall redox equations from reactions in acidic conditions LO3: To construct balanced half equations and overall redox equations from reactions in alkaline conditions (stretch & challenge) Lesson 3: LO1: To understand what a redox titration is. LO2: To describe the practical techniques and procedures used to carry out redox titrations involving Fe2+ /MnO4- LO3: To calculate structured titration questions based on experimental results of redox titrations involving Fe2+ /MnO4- and its derivatives Lesson 4: LO1: To describe the practical techniques and procedures used to carry out redox titrations for I2/S2O32- LO2: To calculate structured titration questions based on experimental results of redox titrations involving I2/S2O32- and non familiar redox systems LO3: To calculate non-structured titration questions based on experimental results of I2/S2O32- Lesson 5: LO1: To describe techniques and procedures used for the measurement of : i) Cell potentials of metals or non-metals in contact with their ions in aqueous solution ii) Ions of the same element in different oxidation states in contact with a Pt electrode Lesson 6: LO1: To use the term standard electrode potential E⦵ including its measurement using a hydrogen electrode LO2: To calculate a standard cell potential by combining two standard electrode potentials LO3: To predict the feasibility of electrode potentials to modern storage cells Lesson 7: LO1. To understand the limitations of predicting the feasibility of a reaction using cell potentials due to kinetics and non-standard conditions LO2. To explain why electrochemical cells may not work based on the limitations of using cell potentials Lesson 8: LO1: To understand the application of the principles of electrode potentials to modern storage cells LO2: To explain that a fuel cell uses the energy from a reaction of a fuel with oxygen to produce a voltage LO3: To derive the reactions that take place at each electrode in a hydrogen fuel cell The teacher will be able to check students have met these learning objectives through starter activities, discussion questions, mini AfL tasks and practice questions 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

3 fully planned lessons (including starter questions and main work tasks) covering the AS Chemistry chapter on Redox Reactions; Lesson 1: Oxidation States Lesson 2: Half Equations Lesson 3: Forming Redox Equations By the end of lesson 1 students will: Recall the rules for oxidation states of uncombined elements and elements in compounds Determine the oxidation states of elements in a redox reaction Identify what substance has been reduced or oxidised in a redox reaction By the end of lesson 2 students will: Understand what a half equation is Explain what a redox equation is Construct half equations from redox equations By the end of lesson 3 students will: Identify what substance has been reduced or oxidised in a redox reaction Construct balanced half equations by adding H+ and H2O Construct full ionic redox equations from half equations 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

3 Full Lesson Bundle on Carbon-13 and Proton NMR Spectroscopy. Suitable for the OCR A Level Chemistry specification. Please review the learning objectives below. Lesson 1: Carbon-13 NMR Spectroscopy To analyse a carbon-13 NMR spectrum of an organic molecule to make predictions about: i) The number of carbon environments in the molecule ii) The different types of carbon environment present from chemical shift values iii) Possible structures for the molecule Lesson 2: Proton NMR Spectroscopy (Part 1) To analyse proton NMR spectra of an organic molecule to make predictions about: i) The number of proton environments in the molecule ii) The different types of proton environment present from chemical shift values Lesson 3: Proton NMR Spectroscopy (Part 2) To analyse proton NMR spectra of an organic molecule to make predictions about: i) The different types of proton environment present from chemical shift values ii) The relative numbers of each type of proton present from the relative peak areas using integration traces or ratio numbers when required iii) The number of non-equivalent protons adjacent to a given proton from the spin-spin splitting pattern, using the n+1 rule iv) Possible structures for the molecule 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