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Related Concept Videos

Oxidations of Aldehydes and Ketones to Carboxylic Acids01:15

Oxidations of Aldehydes and Ketones to Carboxylic Acids

Oxidation of aldehydes and ketones results in the formation of carboxylic acids. Aldehydes, bearing hydrogen next to the carbonyl group, are easily oxidized compared to ketones. This is because an aldehydic proton can easily be abstracted during oxidation.
Aldehydes readily undergo oxidation in strong oxidizing agents such as potassium permanganate and chromic acid. The oxidation can also be carried out using mild oxidizing agents such as silver oxide. In fact, aldehydes can be easily oxidized...
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

Alkenes can be dihydroxylated using potassium permanganate. The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
Oxidation of Alcohols02:37

Oxidation of Alcohols

In this lesson, the oxidation of alcohols is discussed in depth. The various reagents used for oxidation of primary and secondary alcohols are detailed, and their mechanism of action is provided.
The process of oxidation in a chemical reaction is observed in any of the three forms:
Oxidative Cleavage of Alkenes: Ozonolysis01:46

Oxidative Cleavage of Alkenes: Ozonolysis

In ozonolysis, ozone is used to cleave a carbon–carbon double bond to form aldehydes and ketones, or carboxylic acids, depending on the work-up.
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism01:13

Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism

Carboxylic acids react with alcohols to yield esters via an acid-catalyzed condensation reaction called Fischer esterification. This is a nucleophilic acyl substitution reaction that proceeds via a tetrahedral intermediate, where a water molecule is eliminated as the leaving group.
Alkynes to Carboxylic Acids: Oxidative Cleavage02:01

Alkynes to Carboxylic Acids: Oxidative Cleavage

Alkynes undergo oxidative cleavage in the presence of oxidizing reagents like potassium permanganate and ozone. The triple bond — one σ bond and two π bonds — is completely cleaved, and the alkyne is oxidized to carboxylic acids. When warm and basic aqueous potassium permanganate is used as an oxidizing agent, alkynes are first converted to carboxylate salts via an unstable α-diketone intermediate. Further, a mild acid treatment protonates the carboxylate anions generating free carboxylic acid...

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Related Experiment Video

Updated: Jul 4, 2026

Two-way Valorization of Blast Furnace Slag: Synthesis of Precipitated Calcium Carbonate and Zeolitic Heavy Metal Adsorbent
11:14

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Published on: February 21, 2017

Spent caustic oxidation using electro-generated Fenton's reagent in a batch reactor.

Nicolas Rodriguez1, Henrik K Hansen, Patricio Nunez

  • 1Departamento de Procesos Quimicos, Biotecnologicos y Ambientales, Universidad Tecnica Federico Santa Maria, Valparaiso, Chile.

Journal of Environmental Science and Health. Part A, Toxic/Hazardous Substances & Environmental Engineering
|June 24, 2008
PubMed
Summary
This summary is machine-generated.

This study demonstrates an effective Electro-Fenton process for reducing chemical oxygen demand (COD) in spent caustic solutions. The optimized method achieved nearly 95% COD removal, offering a viable wastewater treatment solution.

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Area of Science:

  • Environmental Chemistry
  • Applied Electrochemistry

Background:

  • Spent caustic solutions pose environmental challenges due to high chemical oxygen demand (COD).
  • Conventional treatment methods may be insufficient for complete COD reduction in these industrial wastewaters.

Purpose of the Study:

  • To investigate the efficacy of the Electro-Fenton process for treating spent caustic solutions.
  • To optimize Electro-Fenton parameters for maximum COD removal.

Main Methods:

  • Laboratory-scale Electro-Fenton treatment of spent caustic solutions.
  • Generation of Fenton's reagent in situ using sacrificial ferrous plates as anodes.
  • Analysis of COD reduction by varying ferrous ion concentration, temperature, and pH.

Main Results:

  • Achieved approximately 95% removal of COD from an initial concentration of 8800 mg L(-1).
  • Optimal conditions identified as pH 4, 40°C, and 100 mg L(-1) ferrous ions with 1 A current.
  • A kinetic rate model provided a closer fit to experimental data than an axial dispersion model.

Conclusions:

  • The Electro-Fenton process is highly effective for treating spent caustic wastewater.
  • Optimized parameters significantly enhance COD reduction efficiency.
  • Kinetic modeling is valuable for understanding and simulating the treatment process.