Resources included (16)

Organic synthesis - OCR AS Chemistry

Functional groups - names and formulae OCR AS Chemistry

Polymers from alkenes OCR AS Chemistry

Haloalkanes OCR AS Chemistry

Alkenes OCR AS Chemistry

Reactions of alkanes OCR AS Chemistry

Introduction to alkanes OCR AS Chemistry

Organic reagents and types of reaction OCR AS Chemistry

Isomerism OCR AS Chemistry

Naming hydrocarbons OCR AS Chemistry

Introduction to organic chemistry OCR AS Chemistry

AS synthetic routes

Chemistry of alcohols OCR AS chemistry

Mass spectrometry – OCR AS Chemistry

Infrared (IR) spectroscopy – OCR AS Chemistry

Identifying compounds from infrared and mass spectra – OCR AS Chemistry
This bundle covers all of the OCR A level chemistry specification section 4.1 (basic concepts and hydrocarbons) and 4.2 (alcohols, haloalkanes and analysis).
The resources included are:
- Introduction to organic chemistry
- Naming hydrocarbons (includes quiz – A Question of naming alkanes)
- Functional groups – names and formulae
- Isomerism
- Organic reagents and types of reaction
- Introduction to alkanes
- Reactions of alkanes
- Alkenes
- Polymers from alkenes
- Chemistry of alcohols
- Haloalkanes
- Organic synthesis
- AS synthetic routes
- Infrared spectroscopy
- Mass spectrometry
- Identifying compounds from infrared and mass spectra
Each topic includes a fully interactive PowerPoint including starter, group activities, questions and plenary along with a worksheet. Answers to all exercises are provided. Some of the resources include a PowerPoint quiz and all are ideal for classroom or home learning.
This bundle is part of a series covering the OCR AS Chemistry specification and relates to the following sections:
Module 4– Core organic chemistry
Part 1 – Basic concepts and hydrocarbons (all)
Part 2 - Alcohols, haloalkanes and analysis (all)
Please review!
Content covered:
Introduction to organic chemistry
• Why carbon is special
• Bonding in organic compounds
• Different types of formulae
• Types of organic compounds
• Functional groups and homologous series
Naming hydrocarbons
• Application of IUPAC rules of nomenclature for systematically naming organic compounds
• Naming alkanes and cycloalkanes
• Naming branched alkanes
• Naming alkenes and branched alkenes
Quiz – A Question of naming alkanes
Functional groups – names and formulae
• Application of IUPAC rules of nomenclature for systematically naming organic compounds
• Practice naming organic compounds including those with functional groups
• Revision of empirical and molecular formula and how to calculate them
• Formulae of compounds with functional groups
Displayed formula
Structural formula
Skeletal formula
Isomerism
• Shapes of alkanes (with model building)
• Definitions of structural isomers, stereoisomers, E/Z isomers and cis-trans isomers
• Classification of isomers with examples
• Structural isomers including chain, position and functional group isomers
• Shapes of alkenes (with model building)
• Restricted rotation around the C=C double bond
• Stereoisomers – E/Z and cis-trans isomers
• Animated illustrations of E/Z isomers
• Criteria for E/Z isomerism and for cis-trans isomerism with examples and learning check
• Cahn-Ingold-Prelog rules for naming E/Z isomers with examples
Organic reagents and types of reaction
• Ways of breaking covalent bonds
Homolytic fission
Heterolytic fission
• Types of organic reagents and their reactions
Nucleophiles
Electrophiles
Radicals
• Introduction to mechanisms
• Curly arrows
• Types of reaction
Addition
Substitution
Elimination
• Classification of reactions
Introduction to alkanes
- Sources and uses of alkanes
- Definitions of fossil fuels and crude oil
- Uses of alkanes as fuels
- Bonding in alkanes
- Formation and rotation of sigma bonds
- Shapes of alkanes
- Intermolecular forces in alkanes in terms of non-polar molecules
- Melting and boiling points of alkanes in terms of London forces
- Effect of chain length and branching on London forces
Reactions of alkanes
- Reactivity of alkanes
- Combustion of alkanes – complete and incomplete
- Balancing combustion equations
- Radicals and dot-and-cross diagrams
- Radical chain reactions
- Radical substitution of alkanes by halogens
- Mechanism including initiation, propagation and termination
- Limitations to the use of radical substitution in synthesis of halogenoalkanes
Alkenes
- Structure and reactivity of alkenes
- The nature of the double bond – sigma and pi bonds
- Explanation of restricted rotation around C=C
- Shape of ethene in terms of electron pair repulsion theory
- Addition reactions of alkenes
- Reactions of ethene and propene including addition of halogens, steam, hydrogen halides and hydrogen
- Test for alkenes with aqueous bromine
- Catalytic addition of hydrogen - mechanism
- Margarine manufacture
- Definition of electrophile
- Electrophilic addition mechanism
- Addition of HX to unsymmetrical alkenes - Markownikoff’s rule and explanation
Polymers from alkenes
- Meaning of the terms addition polymer and monomer
- the formation of poly(ethene)
- General equation for polymer formation
- Identifying the monomer from the repeat unit of the monomer
- Disposal of waste polymers by recycling, cracking and combustion
- Bioplastics
- Biodegradable polymers
- Photodegradable polymers
Chemistry of alcohols
- Comparing methods of making ethanol
- Naming alcohols
- Physical properties of alcohols, in terms of hydrogen bonding
- Primary, secondary and tertiary alcohols
- Substitution reaction of alcohols
- Oxidation of alcohols
- Elimination (dehydration) reaction of alcohols
- Reactions of primary, secondary and tertiary alcohols
- Animated mechanisms
- Reaction classification
- Reagents and conditions
- Structural equations
- Key definitions
Haloalkanes
- Naming haloalkanes
- Reactivity of haloalkanes general equation for polymer formation
- Uses of haloalkanes
- Nucleophilic substitution reactions of haloalkanes including hydrolysis
- Mechanism of nucleophilic substitution
- Experiment to compare rates of hydrolysis of different haloalkanes
- Explaining the different rates of hydrolysis
- Organohalogen compounds and the environment
- Destruction of ozone by CFCs
Organic synthesis
- Revision of functional groups
- Techniques for preparation and purification of organic liquids
- Heating under reflux
- Distillation
- Separation of immiscible liquids using a separating funnel
- Use of drying agents
- Stages in the preparation and purification of an organic liquid
- Tests for functional groups
- Compounds with more than one functional group
- Strategies for organic synthesis with examples
AS synthetic routes
- AS synthetic routes
- Animated mechanisms
- Key definitions
- Heating under reflux
- Distillation
- Reaction classification
- Reagents and conditions
- Structural equations
Infrared spectroscopy
- Introduction to spectroscopy linked to the electromagnetic spectrum
- Meaning of wavenumber and transmittance
- Molecular vibrations
- Bond stretching
- Fingerprint region of spectrum
- Types and shapes of peaks
- Infrared and global warming
- The greenhouse effect and greenhouse gases
- Interpreting the infrared spectrum
- Examples of IR spectra with animated explanation linking peaks to structure
- Uses of infrared spectroscopy
Mass spectrometry
- Animated diagram and description of a mass spectrometer
- Meaning of m/z
- Relative intensity
- Base peak
- Molecular ion
- M+1 peak
- Fragments
- Interpreting the mass spectrum
- Mass spectrum of ethanol
- Animations of formation of fragments from ethanol
- Summary of fragments for ethanol
- Examples of mass spectra with animated explanation linking peaks to structure
- Interpretation of mass spectrum of unknown compound leading to its identification
Identifying compounds from infrared and mass spectra
- Calculating empirical formula from % composition
- Calculating molecular formula from empirical formula and molar mass, using the molecular ion peak on the mass spectrum
- Using the infrared (IR) spectrum to identify bond stretches and hence functional group(s) present
- Drawing structural formulae consistent with the molecular formula and IR data
- Using mass spectrum to distinguish between the suggested structural formulae
- Identifying fragments in the mass spectrum
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