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strong base used in organic chemistry for the deprotonation of weakly acidic compounds Manganese dioxide: used as a pigment and as a precursor to other manganese compounds; used as a reagent in organic synthesis for the oxidation of allylic alcohols Meta-Chloroperoxybenzoic acid: used as an oxidant in organic synthesis Methyl tert-butyl ether
This category was created to provide a "home" for inorganic compounds (such as NaBH 4) that are widely used in stoichiometric quantities in organic chemistry, but widely used organic reagents (such as oxalyl chloride) may belong here also. This category is not for catalysts such as Pd.
Folin–Ciocalteu reagent; Formox process; Forster reaction; Forster–Decker method; Fowler process; Franchimont reaction; Frankland synthesis; Frankland–Duppa reaction; Fráter–Seebach alkylation; Free radical halogenation; Freund reaction; Friedel–Crafts acylation; Friedel–Crafts alkylation; Friedländer synthesis; Fries rearrangement
Organic reactions machine-readable reaction schemes "ORD" [8] 2,000,000 OrgSyn Organic Syntheses: Organic Syntheses, Inc. Reliable chemical reactions Searchable experimental procedures Peer reviewed "OrgSyn search". PDB PDBe Protein Data Bank in Europe EMBL-EBI: has some chemicals as well as proteins "PDBe". PATENTSCOPE: WIPO "PATENTSCOPE ...
In chemistry, a reagent (/ r i ˈ eɪ dʒ ən t / ree-AY-jənt) or analytical reagent is a substance or compound added to a system to cause a chemical reaction, or test if one occurs. [1] The terms reactant and reagent are often used interchangeably, but reactant specifies a substance consumed in the course of a chemical reaction. [ 1 ]
Organic chemistry has a strong tradition of naming a specific reaction to its inventor or inventors and a long list of so-called named reactions exists, conservatively estimated at 1000. A very old named reaction is the Claisen rearrangement (1912) and a recent named reaction is the Bingel reaction (1993).
HMPA is a ligand in the useful reagents based on molybdenum peroxide complexes, for example, MoO(O 2) 2 (HMPA)(H 2 O) is used as an oxidant in organic synthesis. [ 9 ] Alternative reagents
Such reagents are useful in the preparation of derivatives of benzaldehyde by formylation and for the conversion of C−OH groups into C−Cl groups. [14] It is especially renowned for the conversion of C=O groups to CCl 2 groups. [15] For example, benzophenone and phosphorus pentachloride react to give the diphenyldichloromethane: [16]
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