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a strong oxidizing agent; can be used to quantitatively determine the total oxidisable organic material in an aqueous sample; a reagent for the synthesis of organic compounds Pyridinium chlorochromate: used to oxidize primary alcohols to aldehydes and secondary alcohols to ketones Pyridinium dichromate (Cornforth reagent)
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 ]
The international pictogram for oxidizing chemicals. Dangerous goods label for oxidizing agents. An oxidizing agent (also known as an oxidant, oxidizer, electron recipient, or electron acceptor) is a substance in a redox chemical reaction that gains or "accepts"/"receives" an electron from a reducing agent (called the reductant, reducer, or electron donor).
For example, when barium chloride (BaCl 2) and magnesium sulfate (MgSO 4) react, the SO 4 2− anion switches places with the 2Cl − anion, giving the compounds BaSO 4 and MgCl 2. Another example of a double displacement reaction is the reaction of lead(II) nitrate with potassium iodide to form lead(II) iodide and potassium nitrate: + +
As a reagent, SMEAH is comparable with lithium aluminium hydride (LAH, LiAlH 4). It is a safer alternative to LAH and related hydrides. SMEAH exhibits similar reducing effects, but does not have the inconvenient pyrophoric nature, short shelf-life, or limited solubility of LAH. Upon contact with air and moisture, SMEAH reacts exothermically but ...
The anion [Ce(NO 3) 6] 2− has T h (idealized O h) molecular symmetry.The CeO 12 core defines an icosahedron. [4]Ce 4+ is a strong one-electron oxidizing agent.In terms of its redox potential (E° ≈ 1.61 V vs. N.H.E.) it is an even stronger oxidizing agent than Cl 2 (E° ≈ 1.36 V).
The primary fluorous deprotecting agent is tetra-n-butylammonium fluoride (TBAF), as its aliphatic chains in help incorporate the fluoride ion into organic solvents. [5] [6] [7] Deprotection with a fluoride ion occurs by an S N 2 mechanism, followed by acidic workup to protonate the resulting alkoxide: ROSiMe 3 + NBu 4 F → RO − + NBu + 4 ...
It is the primary reactant in Yamaguchi esterification. 2,4,6-Trichlorobenzoyl chloride readily reacts with alcohols. This newly formed reagent, when mixed with a stoichiometric amount of 4-dimethylaminopyridine, cyclizes and forms esters. This reaction creates 2,4,6-trichlorobenzoic acid as a byproduct.