58 relations: Achillea millefolium, Acid dissociation constant, Angewandte Chemie, Annulation, Aromaticity, Artemisia (genus), BINAP, Burgess reagent, Chloranil, Chromophore, Cycloaddition, Cyclodecapentaene, Cycloheptatriene, Cyclopentadiene, Cyclopentadienyl, Debye, Dehalogenation, Dehydrohalogenation, Diazomethane, Dimethylformamide, Dipole, Elimination reaction, Ethyl diazoacetate, Friedel–Crafts reaction, Guaiazulene, Hückel's rule, Helicene, Helvetica Chimica Acta, Indane, Insertion reaction, Journal of Chemical Education, Kasha's rule, Ketene, Keto–enol tautomerism, Leopold Ružička, Luche reduction, Matricaria chamomilla, Naphthalene, Naphthol, Nucleophile, Oil of guaiac, One-pot synthesis, Organic compound, Organic redox reaction, Organic synthesis, Organometallic chemistry, Palladium(II) acetate, Phenol, Phosphate, Pi bond, ..., Polymethylhydrosiloxane, Safety data sheet, Sodium borohydride, Steam distillation, Synthon, Tropylium cation, Valence isomer, Vetivazulene. Expand index (8 more) »
Achillea millefolium
Achillea millefolium, commonly known as yarrow or common yarrow, is a flowering plant in the family Asteraceae.
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Acid dissociation constant
An acid dissociation constant, Ka, (also known as acidity constant, or acid-ionization constant) is a quantitative measure of the strength of an acid in solution.
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Angewandte Chemie
Angewandte Chemie (meaning "Applied Chemistry") is a weekly peer-reviewed scientific journal that is published by Wiley-VCH on behalf of the German Chemical Society (Gesellschaft Deutscher Chemiker).
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Annulation
In organic chemistry annulation (from the Latin anellus for "little ring"; occasionally annelation) is a chemical reaction in which a new ring is constructed on a molecule.
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Aromaticity
In organic chemistry, the term aromaticity is used to describe a cyclic (ring-shaped), planar (flat) molecule with a ring of resonance bonds that exhibits more stability than other geometric or connective arrangements with the same set of atoms.
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Artemisia (genus)
Artemisia is a large, diverse genus of plants with between 200 and 400 species belonging to the daisy family Asteraceae.
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BINAP
BINAP (2,2'-bis(diphenylphosphino)-1,1'-binaphthyl) is an organophosphorus compound.
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Burgess reagent
The Burgess reagent (methyl N-(triethylammoniumsulfonyl)carbamate) is a mild and selective dehydrating reagent often used in organic chemistry.
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Chloranil
Chloranil is a quinone with the molecular formula C6Cl4O2.
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Chromophore
A chromophore is the part of a molecule responsible for its color.
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Cycloaddition
A cycloaddition is a pericyclic chemical reaction, in which "two or more unsaturated molecules (or parts of the same molecule) combine with the formation of a cyclic adduct in which there is a net reduction of the bond multiplicity." The resulting reaction is a cyclization reaction.
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Cyclodecapentaene
Cyclodecapentaene or annulene is an annulene with molecular formula C10H10.
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Cycloheptatriene
Cycloheptatriene (CHT) is an organic compound with the formula C7H8.
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Cyclopentadiene
Cyclopentadiene is an organic compound with the formula C5H6.
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Cyclopentadienyl
Cyclopentadienyl can refer to.
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Debye
The debye (symbol: D) is a CGS unit (a non-SI metric unit) of electric dipole momentElectric dipole moment is defined as charge times displacement: |- |height.
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Dehalogenation
Dehalogenation is a chemical reaction that involves the cleavage of C-Halogen bond to form product.
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Dehydrohalogenation
Dehydrohalogenation is a chemical reaction that involves removal of (elimination of) a hydrogen halide from a substrate.
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Diazomethane
Diazomethane is the chemical compound CH2N2, discovered by German chemist Hans von Pechmann in 1894.
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Dimethylformamide
Dimethylformamide is an organic compound with the formula (CH3)2NC(O)H.
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Dipole
In electromagnetism, there are two kinds of dipoles.
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Elimination reaction
An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one or two-step mechanism.
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Ethyl diazoacetate
Ethyl diazoacetate (N.
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Friedel–Crafts reaction
The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring.
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Guaiazulene
Guaiazulene, also azulon or 1,4-dimethyl-7-isopropylazulene, is a dark blue crystalline hydrocarbon.
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Hückel's rule
In organic chemistry, Hückel's rule estimates whether a planar ring molecule will have aromatic properties.
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Helicene
In organic chemistry, helicenes are ortho-condensed polycyclic aromatic compounds in which benzene rings or other aromatics are angularly annulated to give helically-shaped molecules.
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Helvetica Chimica Acta
Helvetica Chimica Acta is a scientific journal founded by the.
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Indane
Indane or indan is a hydrocarbon petrochemical compound, with formula C9H10.
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Insertion reaction
An insertion reaction is a chemical reaction where one chemical entity (a molecule or molecular fragment) interposes itself into an existing bond of typically a second chemical entity e.g.: The term only refers to the result of the reaction and does not suggest a mechanism.
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Journal of Chemical Education
The Journal of Chemical Education is a monthly peer-reviewed academic journal available in both print and electronic versions.
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Kasha's rule
Kasha's rule is a principle in the photochemistry of electronically excited molecules.
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Ketene
A ketene is an organic compound of the form R′R″C.
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Keto–enol tautomerism
In organic chemistry, keto–enol tautomerism refers to a chemical equilibrium between a keto form (a ketone or an aldehyde) and an enol (an alcohol).
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Leopold Ružička
Leopold Ružička (13 September 1887 – 26 September 1976) was a Croatian-Swiss scientist and joint winner of the 1939 Nobel Prize in Chemistry who worked most of his life in Switzerland.
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Luche reduction
Luche reduction is the selective organic reduction of α,β-unsaturated ketones to allylic alcohols with sodium borohydride (NaBH4) and lanthanide chlorides, mainly cerium(III) chloride (CeCl3), in methanol or ethanol.
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Matricaria chamomilla
Matricaria chamomilla (synonym: Matricaria recutita), commonly known as chamomile (also spelled camomile), Italian camomilla, German chamomile, Hungarian chamomile (kamilla), wild chamomile or scented mayweed, is an annual plant of the composite family Asteraceae.
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Naphthalene
Naphthalene is an organic compound with formula.
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Naphthol
Naphthol may refer to.
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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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Oil of guaiac
Oil of guaiac is a fragrance ingredient used in soap and perfumery.
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One-pot synthesis
In chemistry a one-pot synthesis is a strategy to improve the efficiency of a chemical reaction whereby a reactant is subjected to successive chemical reactions in just one reactor.
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Organic compound
In chemistry, an organic compound is generally any chemical compound that contains carbon.
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Organic redox reaction
Organic reductions or organic oxidations or organic redox reactions are redox reactions that take place with organic compounds.
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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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Organometallic chemistry
Organometallic chemistry is the study of organometallic compounds, chemical compounds containing at least one chemical bond between a carbon atom of an organic molecule and a metal, including alkaline, alkaline earth, and transition metals, and sometimes broadened to include metalloids like boron, silicon, and tin, as well.
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Palladium(II) acetate
Palladium(II) acetate is a chemical compound of palladium described by the formula n, abbreviated n. It is more reactive than the analogous platinum compound.
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Phenol
Phenol, also known as phenolic acid, is an aromatic organic compound with the molecular formula C6H5OH.
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Phosphate
A phosphate is chemical derivative of phosphoric acid.
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Pi bond
In chemistry, pi bonds (π bonds) are covalent chemical bonds where two lobes of an orbital on one atom overlap two lobes of an orbital on another atom.
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Polymethylhydrosiloxane
Polymethylhydrosiloxane (PMHS) is a polymer with the general structure -(CH3(H)Si-O)-.
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Safety data sheet
A safety data sheet (SDS), material safety data sheet (MSDS), or product safety data sheet (PSDS) is an important component of product stewardship, occupational safety and health, and spill-handling procedures.
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Sodium borohydride
Sodium borohydride, also known as sodium tetrahydridoborate and sodium tetrahydroborate, is an inorganic compound with the formula NaBH4.
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Steam distillation
Steam distillation is a special type of distillation (a separation process) for temperature sensitive materials like natural aromatic compounds.
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Synthon
In retrosynthetic analysis, a synthon is a destructural unit within a molecule which is related to a possible synthetic operation.
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Tropylium cation
In organic chemistry, the tropylium ion is an aromatic species with a formula of +. Its name derives from the molecule tropine (itself named for the molecule atropine).
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Valence isomer
In organic chemistry, two molecules are valence isomers when they are constitutional isomers that can interconvert through pericyclic reactions.
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Vetivazulene
Vetivazulene is an azulene derivate obtained from vetiver oil.
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Redirects here:
Azulenes, Azulenol, Hydroxyazulene, Pfau-Plattner azulene synthesis, Pfau–Plattner azulene synthesis.
References
[1] https://en.wikipedia.org/wiki/Azulene