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25 relations: Acetylene, Alkene, Alkylation, Allene, Boron trifluoride, Chemical species, Copper(I) cyanide, Double bond, Electrophile, Enantiomer, Epoxide, Gilman reagent, Grignard reaction, Ketone, Lewis acids and bases, Magnesium, Magnesium bromide, Nucleophile, Organic Reactions, Organic synthesis, Organolithium reagent, Pheromone, Racemization, Stoichiometry, Yoshito Kishi.
Acetylene
Acetylene (systematic name: ethyne) is the chemical compound with the formula C2H2.
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Alkene
In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.
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Alkylation
Alkylation is the transfer of an alkyl group from one molecule to another.
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Allene
An allene is a compound in which one carbon atom has double bonds with each of its two adjacent carbon centres.
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Boron trifluoride
Boron trifluoride is the inorganic compound with the formula BF3.
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Chemical species
A chemical species is a chemical substance or ensemble composed of chemically identical molecular entities that can explore the same set of molecular energy levels on a characteristic or delineated time scale.
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Copper(I) cyanide
Copper(I) cyanide is an inorganic compound with the formula CuCN.
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Double bond
A double bond in chemistry is a chemical bond between two chemical elements involving four bonding electrons instead of the usual two.
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Electrophile
In organic chemistry, an electrophile is a reagent attracted to electrons.
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Enantiomer
In chemistry, an enantiomer, also known as an optical isomer (and archaically termed antipode or optical antipode), is one of two stereoisomers that are mirror images of each other that are non-superposable (not identical), much as one's left and right hands are the same except for being reversed along one axis (the hands cannot be made to appear identical simply by reorientation).
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Epoxide
An epoxide is a cyclic ether with a three-atom ring.
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Gilman reagent
A Gilman reagent is a lithium and copper (diorganocopper) reagent compound, R2CuLi, where R is an alkyl or aryl.
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Grignard reaction
The Grignard reaction (pronounced) is an organometallic chemical reaction in which alkyl, vinyl, or aryl-magnesium halides (Grignard reagents) add to a carbonyl group in an aldehyde or ketone.
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Ketone
In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.
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Lewis acids and bases
A Lewis acid is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct.
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Magnesium
Magnesium is a chemical element with symbol Mg and atomic number 12.
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Magnesium bromide
Magnesium bromide (MgBr2) is a chemical compound of magnesium and bromine that is white and deliquescent.
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Nucleophile
Nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction.
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Organic Reactions
Organic Reactions is a secondary reference which synthesizes the organic chemistry literature around particular chemical transformations.
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Organic synthesis
Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.
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Organolithium reagent
Organolithium reagents are organometallic compounds that contain carbon – lithium bonds.
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Pheromone
A pheromone (from Ancient Greek φέρω phero "to bear" and hormone, from Ancient Greek ὁρμή "impetus") is a secreted or excreted chemical factor that triggers a social response in members of the same species.
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Racemization
In chemistry, racemization is the conversion of an enantiomerically pure mixture (one where only one enantiomer is present) into a mixture where more than one of the enantiomers are present.
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Stoichiometry
Stoichiometry is the calculation of reactants and products in chemical reactions.
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Yoshito Kishi
is the Morris Loeb Professor of Chemistry at Harvard University.
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References
[1] https://en.wikipedia.org/wiki/Reactions_of_organocopper_reagents
