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OCR A level Chemistry: Aromatic Compounds
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
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GCSE Chemistry: Alkenes
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
Bundle
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OCR A level Chemistry: Amines, Amino Acids, and Polymers
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
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GCSE Chemistry: Alcohols
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
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GCSE Chemistry: Electrolysis of Solutions
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
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A level Chemistry: Proton NMR Spectroscopy
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)
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A Level Chemistry: Electrophilic Substitution Reactions of Benzene
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
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A Level Chemistry: Carbonyl Compounds
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)
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GCSE Chemistry: Carboxylic Acids
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
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A Level Chemistry: Directing Group for Benzene
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
Bundle
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OCR A level Chemistry: Organic Synthesis
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
Bundle
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OCR A level Chemistry: Chromatography and Spectroscopy
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
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GCSE Chemistry: Polymers
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.
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OCR Applied Science: 4.3 Isomers
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.
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OCR AS Chemistry: Organohalogen Compounds
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
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A level Chemistry: Condensation Polymers
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
Bundle
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OCR A Level Chemistry: Module 6 Organic Chemistry and Analysis
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
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OCR Applied Science: 4.4 Large Complex Carbon Molecules
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
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OCR Applied Science: 4.2 Polymers and Carbon Compounds
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)
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OCR Applied Science: 4.1 Principles of Carbon Chemistry
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