EL(e),(f),(m),(n),(v),(w)

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Presentation transcript:

EL(e),(f),(m),(n),(v),(w) Atomic structure, fusion reactions, mass spec, isotopes EL(a),(g),(h),(x) Atomic spectra, electron configuration, the periodic table EL(e),(f),(m),(n),(v),(w) Covalent bonding and shapes of molecules EL(i),(j),(k) Relative masses, amount of substance, equations EL(a),(b),(d) Ions & salts, Group 2, metallic bonding EL(d),(l),(o),(p),(q),(r), (s),(t),(u) Acid–base titrations EL(b),(c),(t) Enthalpy changes, Hess’ law, bond enthalpy DF(a),(d),(e),(f),(g) Hydrocarbons, cracking, catalysts DF(h),(i),(j),(l),(m),(r) Alkenes, polymers & isomerism DF(b),(c),(m),(o),(p),(q),(s),(t) Gas volume, combustion, pollutants, fuels DF(a),(k),(n),(u) Halogen chemistry, redox chemistry & electrolysis ES(b),(c),(d),(e),(f),(g), (h),(i),(j),(k) Equilibrium, chlorine & halides, atom economy ES(a),(f),(l),(m),(n),(o), (p),(q)

OZ(o),(p),(r),(s),(t),(u) ppm OZ(i) The EM spectrum, energy and matter, ozone & radicals OZ(o),(p),(r),(s),(t),(u) Reaction rates & catalysts OZ(e),(f),(g),(h),(q) Intermolecular bonding, haloalkanes OZ(a),(b),(c),(d),(j),(k) Nucleophilic substitution OZ(j),(k),(l),(m),(n),(q) Alcohols, phenols, carboxylic acids and esters WM(a),(b),(c),(d),(f),(h) MS and IR WM(i),(j) Organic preparation and green chemistry WM(e),(g) Nitrogen chemistry CI(j) Equilibrium CI(f),(h) Kinetics and industrial processes CI(a),(b),(c),(d),(e),(g), (i),(k) Condensation polymers, amines & amides PL(h),(j),(k),(l),(m),(n), (o),(p)

PL(a),(b),(e),(f),(g),(i),(q) PL(c),(d) Amino acids, proteins, isomerism, enzyme kinetics PL(a),(b),(e),(f),(g),(i),(q) DNA and RNA PL(c),(d) NMR & combined spectroscopic techniques PL(r),(s),(t) Solutions & enthalpy O(a),(b),(c) The greenhouse effect, acid–base, solubility product O(i),(j),(h),(k),(l),(m),(n) Entropy O(d),(e),(f),(g) Redox titrations, transition metals DM(a),(b),(g),(h),(i),(j), (k),(l),(m),(n) Electrochemistry DM(c),(d),(f) Delocalisation & colour, benzene chemistry, azo dyes CD(a),(d),(e),(g),(h),(m) Fats & oils CD(c) Gas–liquid chromatography, carbonyls, organic synthesis CD(f),(i),(j),(k),(l),(n)