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Chirality Books

Organic Chemistry, 11th Edition

Author: Francis Carey, Robert Giuliano, Neil Allison, Susan Bane

School: Edo University

Department: Science and Technology

Course Code: CHM123

Topics: Organic Chemistry, alkanes, cycloalkanes, chirality, alcohols, alkyl halides, Nucleophilic Substitution, alkenes, elimination reactions, alkynes, free radicals, arenes, aromaticity, Nucleophilic Substitution. electrophilic Substitution, Spectroscopy, Organometallic Compounds, alcohols, diols, thiols, Ethers, Epoxides, Sulfides, Aldehydes, Ketones, Carboxylic Acids, Nucleophilic Acyl Substitution, enols, enotates, Amines, Carbohydrates, lipid amino acids, peptides, proteins, Nucleosides, Nucleotides, Nucleic Acids, Synthetic Polymers, ionic bonds, covalet bonds, Lewis formula, octet rules

Shriver & Atkin's inorganic chemistry

Author: Peter Atkins, Tina Overton, Jonathan Rourke, Mark weller, Fraser Armstrong, Michael Hagerman

School: University of Ibadan

Department: Science and Technology

Course Code: CHE126

Topics: Inorganic chemistry, atomic structure, atomic orbitals, molecular structure, bonding, Lewis structure, valence bond theory, Molecular orbital theory, ionic solids, ionic bonding, semiconduction, acid, base, Brønsted acidity, Lewis acidity, oxidation, reduction, reduction potentials, redox stability, Molecular symmetry, isomerism, coordination compounds, chirality, spectroscopy, chemical analysis, Magnetometry, periodic trends, Group 1 elements, Group 2 elements, hydrogen, Group 13 elements, Group 15 elements, Group 14 elements, Group 16 elements, d-Block elements, Representative compounds, Electronic spectra, Magnetism, Coordination chemistry, Ligand substitution reactions, Ligand substitution, Redox reactions, Photochemical reactions, Lanthanoid chemistry, Actinoid chemistry, ligands, Solid-state chemistry, materials chemistry, Metal oxides, nitrides, fluorides, Chalcogenides, intercalation compounds, Hydrides, inorganic pigments, Semiconductor chemistry, Molecular materials, fullerides, catalysis, Homogeneous catalysis, Heterogeneous catalysis, Hybrid catalysis, Characterization, fabrication, Nanomaterials, nanoscience, nanotechnology, Self-assembled nanostructures, Bioinorganic nanomaterials, Biological inorganic chemistry, Catalytic processes, Biological cycles, Chelation therapy, nitrogen cycle, hydrogen cycle, acid-base catalysis, Tethered catalysts, Electrocatalysis, Alkene polymerization, Ammonia synthesis, Hydroformylation, Alkene metathesis

Amino acids

Author: Ganiyat Oloyede

School: University of Ibadan

Department: Science and Technology

Course Code: CHE276

Topics: Chemistry, Amino acids, Chirality, amino acids classification, Standard Amino Acids, Hydrophobic amino acids, non-polar side chains Amino acids, polar side chains Amino acids, acidic side chains Amino acids, Nonstandard Amino Acids, Amino Acid Stereochemistry, Fischer projections, amino acids Isoelectric point, amino acid properties, amino acids synthesis, α-halo acids amination, Malonic ester Synthesis, Gabriel phthalimide Synthesis, Phthalimido malonic ester method, Strecker Synthesis, peptide bond, amino acid use, amino acid mixtures analysis

Organic Chemistry

Author: Robert thornton morrison, Robert Neilson Boyd

School: University of Ibadan

Department: Science and Technology

Course Code: CHE276

Topics: Organic Chemistry, chemical bond, quantum mechanics, atomic orbitals, electronic configuration, Pauli exclusion principle, molecular orbitals, covalent bond, hybrid orbitals, intramolecular forces, bond dissociation energy, homolysis, heterolysis, bonds polarity, melting point, intermolecular force, boiling point, solubility, acids, bases, isomerism, activation energy, hydrocarbons, methane structure, oxidation, heat of combustion, chlorination control, relative reactivity, reaction mechanisms, chlorination, free radicals, chain reactions inhibitors, transition state, molecular formula, chlorofluorocarbons, qualitative elemental analysis, quantitative elemental analysis, Alkene, free-radical substitution, ethane structure, Higher alkanes, alkyl groups, industrial source, Grignard reagent, halogenation, free radical stability, combustion, greenhouse effect, pyrolysis, cracking, alkane analysis, stereochemistry, stereoisomers, isomer number, tetrahedral carbon, optical activity, plane-polarized light, polarimeter, specific rotation, enantiomerism, chirality, chiral center, enantiomers, racemic modification, Diastereomers, meso structures, conformational isomers, optical purity, Alkyl halides, Nucleophilic aliphatic substitution, homolytic chemistry, heterolytic chemistry, Carbocations, Carbocations structure, alkyl halides analysis, alcohols, ethers, alcohol nomenclature, carbohydrates fermentation, Ethanol, alcohol preparation, alcohol reaction, alcohol oxidation, ethers preparation, Secondary Bonding, carbon-carbon double bond, Unsaturated hydrocarbon, ethylene structure, Propylene, Hybridization, orbital size, butylene, Geometric isomerism, alcohol dehydration, alkene reaction, hydrogen bromide addition, Hydrogenation, Electrophilic addition, Oxymercuration-demercuration, Hydroboration-oxidation, Alkene Free-radical polymerization, allylic Nucleophilic substitution, dienes, isoprene, isoprene rule, acetylene, Cyclic Aliphatic Compounds, cyclic compound stereoisomerism, cyclic ether, crown ethers, aromaticity, Benzene, aliphatic compounds, aromatic compounds, benzene structure, Kekule structure, Benzene ring, aromatic character, polynuclear aromatic hydrocarbons, Naphthalene, Quantitative elemental analysis, Electrophilic Aromatic Substitution, Friedel-Crafts alkylation mechanism, naphthalene electrophilic substitution, Aromatic-Aliphatic Compounds, Arenes, Spectroscopy, mass spectrum, electromagnetic spectrum, nuclear magnetic resonance spectrum, coupling consonants, chemical shift, aldehydes, ketones, Cannizaro reaction, Grignard reagents addition, Tetrahydropyranyl ethers, Iodoform test, Carboxylic Acids, Grignard synthesis, Dicarboxylic acids, acid chlorides, acid anhydrides, amides, esters, Transesterification, Aldol condensation, Wittig reaction, Crossed Claisen condensation, halides, ammonolysis, amide Hofmann degradation, Heterocyclic amines

Principles of Stereochemistry

Author: CHM112

School: University of Ilorin

Department: Science and Technology

Course Code: CHM112

Topics: Enantiomers, Chirality, Asymmetric Carbon, Stereocenters, Symmetry

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