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OCR A level Chemistry: Aromatic Compounds
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OCR A level Chemistry: Aromatic Compounds

4 Resources
OCR A level Chemistry: Aromatic Compounds is apart of the Module 6: Organic Chemistry and Analysis. All presentations come with worked examples, solutions and homeworks Molecular, empirical, skeletal formula for benzene. The Kekulé model for benzene Evidence against the Kekule model The delocalised model for benzene Nomenclature for benzene rings and aromatic (arene) compounds Naming benzene containing compounds Drawing benzene containing compounds Defining an electrophile Substitution reactions Nitration of Benzene Reaction mechanisms Halogenation of Benzene Common Halogen Carriers Friedel-Crafts Alkylation Reactions Acyl Chloride Acylation Reactions of Benzene Reactivity of Alkenes and Arenes Naming phenols Distinguishing between phenols and alcohols Distinguishing between phenols and alkenes Distinguishing between phenols and carboxylic acids Phenol as a weak acid Electrophilic reactions with phenols Comparing and explaining the reactivity of phenols and benzene Naming positions on the aromatic ring Activating groups and deactivating groups 2-and-4-directing and 3-directing groups ortho-and-para directing and meta directing groups Two-step synthesis routes for benzene using directing groups. Nitration of benzene Halogenation of benzene Friedel-Crafts Alkylation of benzene
GCSE Chemistry: Alkenes
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GCSE Chemistry: Alkenes

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This PowerPoint presentation with worked examples and student questions covers: • Unsaturated hydrocarbons • Comparing alkanes and alkenes • Mnemonic device for naming alkenes • General formula for alkenes • Completing addition reactions for alkenes
OCR A level Chemistry: Amines, Amino Acids, and Polymers
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OCR A level Chemistry: Amines, Amino Acids, and Polymers

3 Resources
OCR A level Chemistry: Aromatic Compounds is apart of the Module 6: Organic Chemistry and Analysis. All presentations come with worked examples, solutions and homeworks. 27.1 Amines 27.2 Amino acids, Amides and Chirality 27.3 Condensation Polymers Aliphatic and aromatic hydrocarbons Amines being derived from ammonia (NH3) Classifying amines as primary, secondary, and tertiary Naming amines Naming ammonium salts Amines neutralisation reactions with acids Preparation of aliphatic amines Preparation of aromatic amines Locants: alpha, beta, and gamma Functional groups of amino acids General formula for amino acids Reactions of amino acids (alkali and acid) Esterification of amino acids Amide functional groups Naming amide molecules Drawing optical isomers Explanation of superimposable and non-superimposable images Identifying chiral centers Recap of addition polymerisation Identifying monomers and repeat units from condensation polymers Polyesters and ester links Polyamides and amide links Polyesters and polyamides formed from one monomer Polyesters and polyamide formed from two monomers Alkali hydrolysis of polyamides and polyesters Acid hydrolysis of polyamides and polyesters
GCSE Chemistry: Alcohols
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GCSE Chemistry: Alcohols

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This PowerPoint presentation with worked examples and student questions covers: • Functional groups of alcohols, alkanes, and alkenes. • Comparing incomplete and complete combustion of alcohols • Mnemonic device for naming alcohols • General formula for alcohols • Drawing the structural formula for alcohols
GCSE Chemistry: Electrolysis of Solutions
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GCSE Chemistry: Electrolysis of Solutions

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This PowerPoint presentation with worked examples and student questions covers: • The position of metals and non-metals on the periodic table • The ions metals and non-metals form • The ion composition of solutions • Electrodes, cations and anions • The products of electrolysis of solutions • Keyword descriptions and revision tips
A level Chemistry: Proton NMR Spectroscopy
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A level Chemistry: Proton NMR Spectroscopy

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OCR A level Chemistry: 29.4 Proton NMR Spectroscopy This PowerPoint is a whole lesson included with student activities, animated answers, homework questions with answers provided. This lesson covers: Identifying the number of different proton environments Identifying the types of proton environment and chemical shifts Integration traces (area of peaks) and relative number of protons The spin-spin splitting pattern (n + 1)
A Level Chemistry: Electrophilic Substitution Reactions of Benzene
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A Level Chemistry: Electrophilic Substitution Reactions of Benzene

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OCR A level Chemistry: 25.2 Electrophilic Substitution Reactions of Benzene This PowerPoint is a whole lesson included with student activities, animated answers, homework questions with answers provided. This lesson covers: Defining an electrophile Substitution reactions Nitration of Benzene Reaction mechanisms Halogenation of Benzene Common Halogen Carriers Friedel-Crafts Alkylation Reactions Acyl Chloride Acylation Reactions of Benzene Reactivity of Alkenes and Arenes
A Level Chemistry: Carbonyl Compounds
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A Level Chemistry: Carbonyl Compounds

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OCR A level Chemistry: 26.1 Carbonyl Compounds This PowerPoint is a whole lesson included with student activities, animated answers, homework questions with answers provided. This lesson covers: The carbonyl group Differentiating between aldehydes and ketones Naming aldehydes and ketones Oxidation of aldehydes Electronegativity and polar bonds Electrophiles, nucleophiles, and nucleophilic addition reactions Reducing carbonyl compounds with sodium tetrahydridoborate(III) (NaH4) Primary and secondary alcohols from carbonyl compounds Reacting carbonyl compounds with hydrogen cyanide (HCN) Reaction mechanisms for nucleophilic addition using (NaBH4) Reaction mechanisms for nucleophilic addition using (HCN)
GCSE Chemistry: Carboxylic Acids
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GCSE Chemistry: Carboxylic Acids

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This PowerPoint presentation with worked examples and student questions covers: • Functional groups of carboxylic acids, alcohols, alkanes, and alkenes. • Mnemonic device for naming carboxylic acids • General formula for carboxylic acids • Drawing the structural formula for carboxylic acids • Carboxylic acids as weak acids and • Acid reactions with bases, metals, and carbonates • Oxidation reactions from alcohols to carboxylic acids
A Level Chemistry: Directing Group for Benzene
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A Level Chemistry: Directing Group for Benzene

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OCR A level Chemistry: 25.4 Directing Group This PowerPoint is a whole lesson included with student activities, animated answers, homework questions with answers provided. This lesson covers: Naming positions on the aromatic ring Activating groups and deactivating groups 2-and-4-directing and 3-directing groups ortho-and-para directing and meta directing groups Two-step synthesis routes for benzene using directing groups. Nitration of benzene Halogenation of benzene Friedel-Crafts Alkylation of benzene
OCR A level Chemistry: Organic Synthesis
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OCR A level Chemistry: Organic Synthesis

3 Resources
OCR A level Chemistry: Organic Synthesis is apart of the Module 6: Organic Chemistry and Analysis. All presentations come with worked examples, solutions and homeworks. 28.1 Carbon-Carbon Bond Formation 28.2 Further Practical Techniques 28.3 Further Synthetic Routes Forming nitriles from haloalkanes Forming nitriles from aldehydes and ketones Forming amines from nitriles (reduction) Forming carboxylic acids from nitriles (hydrolysis) Friedel-Crafts alkylation of benzene Acylation of benzene with acyl chloride Filtration under reduced pressure Purification through Recrystallisation Preparation of Melting Point Sample Melting point determination with an electric heater Melting point determination with a Thiele tube Functional groups Reactions of benzenes Reactions of phenols Common reactions between different functional groups Reaction conditions and reagents
OCR A level Chemistry: Chromatography and Spectroscopy
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OCR A level Chemistry: Chromatography and Spectroscopy

6 Resources
OCR A level Chemistry: Chromatography and Spectroscopy is apart of the Module 6: Organic Chemistry and Analysis. All presentations come with worked examples, solutions and homeworks. 29.1 Chromatography and Functional Group Analysis 29.2 Nuclear Magnetic Resonance (NMR) Spectroscopy 29.3 Carbon-13 NMR Spectroscopyy 29.4 Proton NMR Spectroscopy 29.5 Interpreting Proton NMR Spectra 29.6 Combined Techniques Thin layer chromatography (TLC) Rf values Gas chromatography (GC) Gas chromatograms Retention time and peak integrations Calibration curves from retention time and relative peak area Differentiation of functional groups: alkene, primary and secondary alcohols, aldehydes, cabonyl compounds, carboxylic acids, and haloalkes. Nuclear Spin Resonance Tetramethylsilane (TMS) Chemical Shift ẟ Identifying different carbon environments The types of carbon environment The amount of chemical shift ẟ / ppm Identifying the number of different proton environments Identifying the types of proton environment and chemical shifts Integration traces (area of peaks) and relative number of protons The spin-spin splitting pattern (n + 1) Predicting proton NMR spectra for molecules Identifying the number of different proton environments Identifying the types of proton environment and chemical shifts Integration traces (area of peaks) and relative number of protons Percentage yield to determine empirical formula Mass spectra Infrared spectra Carbon-13 NMR spectra Proton NMR spectra
GCSE Chemistry: Polymers
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GCSE Chemistry: Polymers

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This PowerPoint presentation with worked examples and student questions covers: • State what is meant by mono- and poly-. • Describe polymerisation and the effects of cross-links in polymers. • Determine a polymer’s repeat units from a monomer’s structural formula.
OCR Applied Science: 4.3 Isomers
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OCR Applied Science: 4.3 Isomers

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This PowerPoint presentation with worked examples and student activities covers: Topic 4.3 of Module 1: Science Fundamentals of the OCR Applied Science Spec. • Stating definitions and comparing structural isomers and stereoisomers. • Condensed structural formula • Lines of symmetry for structural isomers • Cis- and Trans isomers • Optical isomers as non-superimposable mirror images. • Wedge and Dash Notation • Identifying chiral centres (asymmetric carbons) • Le Bel-van’t Hoff rule • Determining the maximum number of isomers.
OCR AS Chemistry: Organohalogen Compounds
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OCR AS Chemistry: Organohalogen Compounds

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OCR AS Chemistry: 15.2 Organohalogen Compounds and the Environment This PowerPoint is a whole lessons included with student activities, animated answers, homework questions with answers provided. This lesson covers: Definitions for CFC (Chlorofluorocarbons) and HCFC (Hydachlorofluorocarbons) Creation of ozone Depletion of ozone with CFCs Reaction steps including initiations and propagation
A level Chemistry: Condensation Polymers
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A level Chemistry: Condensation Polymers

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OCR A level Chemistry: 27.3 Condensation Polymers This PowerPoint is a whole lesson included with student activities, animated answers, homework questions with answers provided. This lesson covers: Recap of addition polymerisation Identifying monomers and repeat units from condensation polymers Polyesters and ester links Polyamides and amide links Polyesters and polyamides formed from one monomer Polyesters and polyamide formed from two monomers Alkali hydrolysis of polyamides and polyesters Acid hydrolysis of polyamides and polyesters
OCR A Level Chemistry: Module 6 Organic Chemistry and Analysis
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OCR A Level Chemistry: Module 6 Organic Chemistry and Analysis

20 Resources
This bundle includes all PowerPoint lessons for Module 6 Organic Chemistry and Analysis. All PowerPoints are whole lessons included with student activities, animated answers, homework questions with answers provided. C25 Aromatic Chemistry Introducing Benzene Electrophilic substitution Reactions The Chemistry of Phenol Directing Groups C26 Carbonyls and Carboxylic Acids Carbonyl Compounds Identifying Aldehydes and ketones Carboxylic acids Carboxylic acid derivatives C27 Amines, Amino Acids and Polymers Amines Amino acids, amides and chirality Condensation Polymers C28 Organic Synthesis Carbon-carbon bond formation Further Practical Techniques Further Synthetic Routes C29 Chromatography and Spectroscopy Chromatography and functional group analysis Nuclear Magnetic Resonance Spectroscopy Carbon-13 NMR Spectroscopy Proton NMR Spectroscopy Interpreting NMR Spectra Combining Techniques
OCR Applied Science: 4.4 Large Complex Carbon Molecules
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OCR Applied Science: 4.4 Large Complex Carbon Molecules

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This PowerPoint presentation with worked examples and student activities covers: Topic 4.4 of Module 1: Science Fundamentals of the OCR Applied Science Spec. Complex carbohydrates (starch, glycogen, cellulose) • Carbohydrates found as monosaccharides, disaccharides, or polysaccharides (monomers, dimers or polymers) • Monomers held together by glycosidic bonds to form dimers and polymers, via condensation reactions • Monosaccharides include glucose, fructose and galactose • Disaccharides include maltose, sucrose and lactose • Polysaccharides include starch, glycogen and cellulose • Cellulose is found in plant cell walls where it provides strength/support and pliability • Starch and glycogen are energy sources Proteins and peptides from amino acids • Dipeptides are formed from two amino acids joined by a peptide bond, via a condensation reaction • Polypeptides are chains of amino acids joined by peptide bonds • Proteins/polypeptides have physiological or functional roles, including enzymes, carrier proteins in the plasma membrane, and structural roles, including collagen and elastin fibres in connective tissue Lipids from fatty acids, glycerol and phosphorus compounds • Monoglycerides, diglycerides and triglycerides are esters of fatty acids and glycerol • An ester bond forms between each fatty acid and the glycerol, via condensation reactions • Phospholipids contain glycerol plus two fatty acids and a phosphate group • Lipids act as an energy source within cells, as an insulation layer around animal organs, in the myelin sheath (found around some nerve fibres/axons) to increase speed of nerve transmission • Phospholipids form a bilayer in the plasma membrane Protein synthesis (transcription, translation) RNA, messenger, ribosomal and transfer • The nucleic acids, DNA and RNA, are polymers of nucleotides • Peptide bonds form between amino acids to create polypeptide chains/proteins • Recall a simple description of protein synthesis
OCR Applied Science: 4.2 Polymers and Carbon Compounds
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OCR Applied Science: 4.2 Polymers and Carbon Compounds

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This PowerPoint presentation with worked examples and student activities covers: Topic 4.2 of Module 1: Science Fundamentals of the OCR Applied Science Spec. Determining the empirical formula for compounds Draw monomers and repeat units using structural and skeletal formula of the following polymers: Polyethene​ Polypropene​ Polylactate​ Polystyrene​ Polyvinyl chloride (PVC)
OCR Applied Science: 4.1 Principles of Carbon Chemistry
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OCR Applied Science: 4.1 Principles of Carbon Chemistry

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This PowerPoint presentation with worked examples and student activities covers: Topic 4.1 of Module 1: Science Fundamentals of the OCR Applied Science Spec. • Alkanes as saturated hydrocarbons containing single C-C and C-H bonds • Alkenes as unsaturated hydrocarbons containing a C=C double bond • Alkynes as unsaturated hydrocarbons containing a C ≡ C triple bond • Name and draw structural and skeletal formulae of the first four members of alkanes, alkenes and alkynes • Aldehydes and ketones as organic compounds containing the C=O group • Name and draw the structural formulae of the first four aldehydes and the first two ketones • Alcohols as organic compounds containing the OH group • Name and draw structural and skeletal formulae of the first four alcohols • Conversion of alcohols to form aldehydes and ketones is classified as an oxidation reaction • Name and draw structural and skeletal formulae of the first four carboxylic acids • Reaction of carboxylic acids with an alkali, to include full equations using structural formulae • Name and draw structural and skeletal formulae of the four C4H8O2 esters • How an ester can be made from a carboxylic acid and an alcohol