OCR A level Physics: Gravitational Fields is apart of the Module 5: Newtonian world and Astrophysics. All presentations come with worked examples, solutions and homeworks. 18.1 Gravitational Fields 18.2 Newton’s law of gravitation 18.3 Gravitational field strength for a point mass 18.4 Kepler’s laws 18.5 Satellites 18.6 Gravitational potential 18.7 Gravitational potential energy The terms: eccentricity, aphelion, perihelion, astronomical unit Kepler’s First Law Kepler’s Second Law Kepler’s Third Law Graphs of T^2 against r^3 to determine the gradient (constant of proportionality, k). Equating (4π)^2/𝐺𝑀 to the gradient (constant of proportionality, k) Key features of geostationary and low polar orbit satellites Conditions for stable orbits for satellites Applying Kepler’s laws to the orbits of satellites Radial and uniformed field Definition of gravitational potential energy Deriving escape velocity Force-Distance graphs for gravitational fields Center of mass and treating spherical objects as point masses Gravitational fields Definition of gravitational potential Applying the gravitational potential equation Graph of gravitational potential against distance (V against r) Combining gravitational potentials from more than one mass

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 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

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