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Summary Of: Alkene

is a stable strained alkene and the orbital misalignment is only 19... but they are driven towards the alkene at high temperatures by... One of the principal methods for alkene synthesis in the laboratory is the... alkene is usually the major product... Another important method for alkene synthesis involves construction of a new carbon... ketone can also be converted to the corresponding alkene via its tosylhydrazone... When an alkene has more than one substituent...

Encyclodia Page On: Alkene

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Olefin fiber | A 3D model of ethylene, the simplest alkene. | | ethylene | organic chemistry | unsaturated | chemical compound | carbon | carbon | double bond | functional groups | homologous series | hydrocarbons | ethylene | International Union of Pure and Applied Chemistry | petrochemical | Aromatic | Ethylene (ethene), showing the pi bond in green. | | covalent bonds | sigma bond | sigma bond | pi bond | covalent bond | kJ | mol | bond length | Angstroms | pm | hybrid orbitals | isomers | cis isomer | cis-but-2-ene | methyl | pi bond | p orbitals | pyramidalization | pyramidal alkene | trans-Cyclooctene | dihedral angle | dipole | D | cis-isomer | cycloheptene | VSEPR | electron | molecular geometry | bond angles | steric strain | nonbonded interactions | functional groups | propylene | alkanes | physical state | molecular mass | ethylene | propylene | butylene | alkanes | single bonds | petrochemical | addition reactions | Catalytic addition of hydrogen | Catalytic | alkanes | catalyst | platinum | nickel | palladium | Raney nickel | alloy | nickel | aluminium | ethylene | ethane | Electrophilic addition | electrophilic addition | Prins reaction | carbonyl | Halogenation | bromine | chlorine | vicinal | bromine number | Hydrohalogenation | hydrohalic acids | HCl | HBr | haloalkanes | Markovnikov's rule | | carbene | carbenoid | cyclopropane | oxidized | oxidizing agents | oxygen | carbon dioxide | Catalytic | percarboxylic | epoxides | ozonolysis | aldehydes | ketones | Sharpless bishydroxylation | Woodward cis-hydroxylation | diols | Polymerization | polymers | polyethylene | polypropylene | radical | cracking | petroleum | zeolite | Cracking of n-octane to give pentane + propene | dehydrogenation | catalytic hydrogenation | Dehydrogenation of butane to give butadiene and isomers of butene | entropy | Catalytic | organometallic compound | triethylaluminium | nickel | cobalt | platinum | elimination | tosylate | triflate | dehydrohalogenation | Saytzeff's rule | An example of an E2 Elimination | alcohols | dehydration | ethanol | CH3CH2OH | H2SO4 | H2C=CH2 | xanthate | Chugaev elimination | Grieco elimination | Boord olefin synthesis | ester pyrolysis | amines | alkylated | Hofmann elimination | amine oxide | Cope reaction | Saytseff | Synthesis of cyclooctene via Cope elimination | sulfones | Ramberg-Bäcklund reaction | aldehyde | ketone | carbanion | Wittig reagent | Ph3P=O | triphenylphosphine | A typical example of the Wittig reaction | Peterson olefination | Julia olefination | phenyl | sulfone | Takai olefination | Tebbe's reagent | McMurry reaction | Barton-Kellogg reaction | sodium methoxide | Bamford-Stevens reaction | Shapiro reaction | Olefin metathesis | olefin metathesis | muscone | Ring-closing metathesis used in synthesis of muscone | Coupling reactions | palladium | Heck reaction | naproxen | Synthesis of naproxen via the Heck reaction | Stille | Suzuki | Negishi | triflate | metalloid | Synthesis of caparratriene using the Suzuki coupling | alkynes | stereoselective | hydrogenation | Lindlar's catalyst | sodium | ammonia | Synthesis of cis- and trans-alkenes from alkynes | carbometalation | rearrangement reactions | olefin metathesis | pericyclic reactions | ene reaction | Cope rearrangement | Cope rearrangement of divinylcyclobutane to cyclooctadiene | Diels-Alder reaction | cyclohexene | IUPAC | alkane | isomers | alkanes | Naming substituted hex-1-enes | | Cis-trans isomerism | Cis-trans | The difference between cis- and trans- isomers | | E-Z notation | CIP rules | The difference between E and Z isomers | | vinyl | allyl | | | Wiktionary | Alpha-olefin | Arenes | aromaticity | Prentice Hall | Pure and Applied Chemistry | doi | doi | 2008 | 01-02 | doi | doi | doi | 2008 | 01-02 | v | Ethene | Propene | Butene | Pentene | Hexene | v | d | Functional groups | Chemical class | Alcohol | Aldehyde | Alkane | Alkyne | Amide | Amine | Azo compound | Benzene derivative | Carboxylic acid | Cyanate | Disulfide | Ester | Ether | Haloalkane | Hydrazone | Imine | Isocyanide | Isocyanate | Ketone | Oxime | Nitrile | Nitro compound | Nitroso compound | Peroxide | Phosphoric acid | Pyridine derivative | Sulfone | Sulfonic acid | Sulfoxide | Thioester | Thioether | Thiol | v | d | Chemistry | Analytical chemistry | Biochemistry | Bioinorganic chemistry | Bioorganic chemistry | Chemical biology | Chemistry education | Click chemistry | Cluster chemistry | Computational chemistry | Electrochemistry | Environmental chemistry | Green chemistry | Inorganic chemistry | Materials science | Medicinal chemistry | Nuclear chemistry | Organic chemistry | Organometallic chemistry | Pharmacy | Physical chemistry | Photochemistry | Polymer chemistry | Solid-state chemistry | Supramolecular chemistry | Theoretical chemistry | Thermochemistry | Wet chemistry | List of biomolecules | List of inorganic compounds | List of organic compounds | Periodic table | Categories | Alkenes | Functional groups | Hydrocarbons |
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Alkene".