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40 relations: Acetone, Alcohol, Aldehyde, Aluminium isopropoxide, Bleach, Carbodiimide, Carbonyl group, Carboxylic acid, Chromium trioxide, Collins reagent, Cornforth reagent, Cyclohexanone, Dess–Martin periodinane, Dimethyl sulfoxide, Diol, Electrophile, Glycol cleavage, Jones oxidation, Ketone, Lead(IV) acetate, Manganese dioxide, N-Methylmorpholine N-oxide, Oppenauer oxidation, Organic reaction, Organic redox reaction, Oxalyl chloride, Oxidation of primary alcohols to carboxylic acids, Oxoammonium-catalyzed oxidation, Parikh–Doering oxidation, Pfitzner–Moffatt oxidation, Potassium permanganate, Pyridinium chlorochromate, Ruthenium tetroxide, Sodium hypochlorite, Sodium periodate, Swern oxidation, TEMPO, Tetrapropylammonium perruthenate, 2,5-Dimethylfuran, 2-Iodoxybenzoic acid.
Acetone
Acetone (systematically named propanone) is the organic compound with the formula (CH3)2CO.
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Alcohol
In chemistry, an alcohol is any organic compound in which the hydroxyl functional group (–OH) is bound to a carbon.
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Aldehyde
An aldehyde or alkanal is an organic compound containing a functional group with the structure −CHO, consisting of a carbonyl center (a carbon double-bonded to oxygen) with the carbon atom also bonded to hydrogen and to an R group, which is any generic alkyl or side chain.
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Aluminium isopropoxide
Aluminium isopropoxide is the chemical compound usually described with the formula Al(O-i-Pr)3, where i-Pr is the isopropyl group (–CH(CH3)2).
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Bleach
Bleach is the generic name for any chemical product which is used industrially and domestically to whiten clothes, lighten hair color and remove stains.
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Carbodiimide
A carbodiimide or a methanediimine is a functional group consisting of the formula RN.
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Carbonyl group
In organic chemistry, a carbonyl group is a functional group composed of a carbon atom double-bonded to an oxygen atom: C.
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Carboxylic acid
A carboxylic acid is an organic compound that contains a carboxyl group (C(.
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Chromium trioxide
Chromium trioxide is an inorganic compound with the formula CrO3.
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Collins reagent
Collins reagent is the complex of chromium(VI) oxide with pyridine in dichloromethane.
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Cornforth reagent
The Cornforth reagent or pyridinium dichromate (PDC) is a pyridinium salt of dichromate with the chemical formula 2.
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Cyclohexanone
Cyclohexanone is the organic compound with the formula (CH2)5CO.
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Dess–Martin periodinane
Dess–Martin periodinane (DMP) is a chemical reagent used to oxidize primary alcohols to aldehydes and secondary alcohols to ketones.
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Dimethyl sulfoxide
Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH3)2SO.
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Diol
A diol or glycol is a chemical compound containing two hydroxyl groups (−OH groups).
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Electrophile
In organic chemistry, an electrophile is a reagent attracted to electrons.
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Glycol cleavage
Glycol cleavage is a specific type of organic chemistry oxidation.
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Jones oxidation
The Jones oxidation is an organic reaction for the oxidation of primary and secondary alcohols to carboxylic acids and ketones, respectively.
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Ketone
In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.
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Lead(IV) acetate
Lead(IV) acetate or lead tetraacetate is a chemical compound with chemical formula Pb(C2H3O2)4.
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Manganese dioxide
Manganese(IV) oxide is the inorganic compound with the formula.
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N-Methylmorpholine N-oxide
N-Methylmorpholine N-oxide (more correctly 4-methylmorpholine 4-oxide), NMO or NMMO is an organic compound.
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Oppenauer oxidation
Oppenauer oxidation, named after Rupert Viktor Oppenauer, is a gentle method for selectively oxidizing secondary alcohols to ketones.
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Organic reaction
Organic reactions are chemical reactions involving organic compounds.
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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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Oxalyl chloride
Oxalyl chloride is a chemical compound with the formula (COCl)2.
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Oxidation of primary alcohols to carboxylic acids
The oxidation of primary alcohols to carboxylic acids is an important oxidation reaction in organic chemistry.
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Oxoammonium-catalyzed oxidation
Oxoammonium-catalyzed oxidation reactions involve the conversion of organic substrates to more highly oxidized materials through the action of an N-oxoammonium species.
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Parikh–Doering oxidation
The Parikh–Doering oxidation is an oxidation reaction that transforms primary and secondary alcohols into aldehydes and ketones, respectively.
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Pfitzner–Moffatt oxidation
The Pfitzner–Moffatt oxidation, sometimes referred to as simply the Moffatt oxidation, is a chemical reaction for the oxidation of primary and secondary alcohols to aldehydes and ketones, respectively.
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Potassium permanganate
Potassium permanganate is an inorganic chemical compound and medication.
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Pyridinium chlorochromate
Pyridinium chlorochromate (PCC) is a yellow-orange salt with the formula.
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Ruthenium tetroxide
Ruthenium tetroxide (Ruthenium(VIII) oxide) is the inorganic compound with the formula RuO4.
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Sodium hypochlorite
No description.
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Sodium periodate
Sodium periodate is an inorganic salt, composed of a sodium cation and the periodate anion.
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Swern oxidation
The Swern oxidation, named after Daniel Swern, is a chemical reaction whereby a primary or secondary alcohol is oxidized to an aldehyde or ketone using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base, such as triethylamine.
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TEMPO
(2,2,6,6-Tetramethylpiperidin-1-yl)oxyl or (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl, commonly known as TEMPO, is a chemical compound with the formula (CH2)3(CMe2)2NO.
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Tetrapropylammonium perruthenate
Tetrapropylammonium perruthenate (TPAP or TPAPR) is the chemical compound described by the formula N(C3H7)4RuO4.
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2,5-Dimethylfuran
2,5-Dimethylfuran is a heterocyclic compound with the formula (CH3)2C4H2O.
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2-Iodoxybenzoic acid
IBX or 2-iodoxybenzoic acid is an organic compound used in organic synthesis as an oxidizing agent.
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References
[1] https://en.wikipedia.org/wiki/Alcohol_oxidation
