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Summary Of: Organic chemistry

Organic chemistry received a boost when it was realized that these compounds could be treated in ways... The crucial breakthrough for the theory of organic chemistry was the concept of chemical structure... The history of organic chemistry continues with the discovery of... the progress of organic chemistry allowed for synthesis of specifically selected compounds or even molecules designed with specific properties... opening up a brand new chapter of organic chemistry with enormous scope... in organic chemistry the relative arrangement of the atoms within a molecule must be added for a full... One important property of carbon in organic chemistry is that it can form certain compounds... is a major category within organic chemistry which is frequently studied by... Others are sometimes put into major groups within organic chemistry and discussed under titles such as...

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Acetic acid is an example. | | carboxylic | functional group | Acetic acid | miscibility | acidity | alkalinity | reactivity | oxidation | radicals | polar | halogens | functional groups | aliphatic | aromatic | alicyclic | organic nomenclature | IUPAC | trivial names | aliphatic | cyclic compounds | Aliphatic compound | homologous series | saturation | alkanes | alkenes | alkynes | octane number | cetane number | Benzene is one of the best-known aromatic compounds as it is one of the simplest aromatics. | | Benzene | alicyclics | aromatics | arenes | cycloalkanes | cycloalkenes | macrocycles | cyclopropane | Aromatic | conjugated | benzene | Kekulé | delocalization | resonance | antiaromaticity | heterocycle | Pyridine | furan | piperidine | tetrahydrofuran | polycyclic compounds | purine | spiro | natural products | Polymer | This swimming board is made of polystyrene, an example of a polymer | | polystyrene | polymerization | monomer | industrial polymers | biopolymers | bakelite | polyethylene | polypropylene | nylon | teflon | polystyrene | polyesters | polymethylmethacrylate | polyvinylchloride | polyisobutylene | rubber | butadiene | chain length | branching | tacticity | homopolymer | heteropolymer | density | tensile strength | Maitotoxin, a complex organic biological toxin. | | Maitotoxin | Biomolecular chemistry | biochemists | biopolymers | proteins | DNA | RNA | polysaccharides | starches | celluloses | amino acids | carbohydrates | nucleic acids | lipids | Krebs cycle | isoprene | steroid | cholesterol | terpenes | terpenoids | alkaloids | latex | rubber | Buckyballs | carbon nanotubes | organosulfur chemistry | organometallic chemistry | organophosphorus chemistry | organosilicon chemistry | The structure of methane by pictorial representation of a Lewis diagram showing the sharing of electronpairs between atomic nuclei in a covalent  bond.  Please do not form the impression from the diagram that the real picture is two-dimensional, because this is not the case. | | methane | Lewis diagram | covalently bonded | catenation | soluble | water | salts | molecular weight | alcohols | carboxylic acids | hydrogen bonding | solvents | ether | ethyl alcohol | petroleum ethers | white spirits | fractions | functional groups | physical chemistry | crystals | organic compounds | unsaturation | double bonds | triple bonds | conjugated | aromatic | Molecular models of caffeine | | caffeine | Organic compounds | functional groups | valence | degree of unsaturation | chemical formula | isomers | mixtures | boiling points | solvents | distillation | crystallization | chromatography | Crystallography | molecular geometry | molecular symmetry | Elemental analysis | Infrared spectroscopy | functional groups | Mass spectrometry | molecular weight | mass spectrum analysis | Nuclear magnetic resonance (NMR) spectroscopy | correlation spectroscopy | Optical rotation | enantiomers | specific rotation | HPLC | UV/VIS spectroscopy | analytical chemistry | Organic reactions | chemical reactions | organic compounds | hydrocarbons | electron affinity | bond strengths | steric hindrance | reactive intermediates | substitution reaction | functional group | nucleophile | Gibbs free energy | enthalpy | side reactions | Organic synthesis | A synthesis designed by E.J. Corey for oseltamivir (Tamiflu). | | E.J. 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This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Organic chemistry".