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Related Concept Videos

Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids02:04

Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids

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Diols are compounds with two hydroxyl groups. In addition to syn dihydroxylation, diols can also be synthesized through the process of anti dihydroxylation. The process involves treating an alkene with a peroxycarboxylic acid to form an epoxide. Epoxides are highly strained three-membered rings with oxygen and two carbons occupying the corners of an equilateral triangle. This step is followed by ring-opening of the epoxide in the presence of an aqueous acid to give a trans diol.
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Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

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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.
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Radical Autoxidation01:20

Radical Autoxidation

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The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...
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Pyruvate Oxidation01:15

Pyruvate Oxidation

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After glycolysis, the charged pyruvate molecules enter the mitochondria via active transport and undergo three enzymatic reactions. These reactions ensure that pyruvate can enter the next metabolic pathway so that energy stored in the pyruvate molecules can be harnessed by the cells.
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...
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Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide02:44

Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

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Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
10.9K
Carboxylic Acids to Methylesters: Alkylation using Diazomethane01:33

Carboxylic Acids to Methylesters: Alkylation using Diazomethane

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Carboxylic acids react with diazomethane in an ether solvent via alkylation at the carboxylate oxygen atom to give methyl esters of the corresponding acid with excellent yields.
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Updated: Sep 18, 2025

Preparation of Biomass-based Mesoporous Carbon with Higher Nitrogen-/Oxygen-chelating Adsorption for CuII Through Microwave Pre-Pyrolysis
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Preparation of Biomass-based Mesoporous Carbon with Higher Nitrogen-/Oxygen-chelating Adsorption for CuII Through Microwave Pre-Pyrolysis

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Oxidant-assisted methane pyrolysis.

Marco Gigantino1, Henry Moise1, Vasudev Haribal2

  • 1Department of Chemical Engineering, Stanford University Stanford CA 94305 USA mcargnello@stanford.edu.

Chemical Science
|June 25, 2025
PubMed
Summary
This summary is machine-generated.

Adding small amounts of oxidants like CO2 or H2O to methane pyrolysis significantly boosts hydrogen and carbon production. This breakthrough prevents catalyst deactivation, paving the way for scalable, low-emission hydrogen generation.

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Area of Science:

  • Chemical Engineering
  • Catalysis
  • Sustainable Energy

Background:

  • Methane pyrolysis offers a scalable route to low-CO2 hydrogen production using existing infrastructure.
  • Catalyst deactivation and carbon buildup are major hurdles for large-scale methane pyrolysis.

Purpose of the Study:

  • To investigate the impact of oxidant addition on methane pyrolysis efficiency and catalyst stability.
  • To overcome catalyst deactivation and carbon deposition challenges in methane pyrolysis.

Main Methods:

  • Methane pyrolysis experiments were conducted in a fluidized bed reactor at 750 °C.
  • Small concentrations of CO2 and H2O were introduced as oxidants with methane over Fe-based catalysts.
  • Catalyst performance and effluent composition were analyzed to assess hydrogen and carbon yields.

Main Results:

  • Addition of CO2 increased carbon yield twofold and hydrogen concentration 7.5-fold compared to pure methane.
  • H2O addition showed similar beneficial effects, preventing catalyst deactivation.
  • Evidence suggests a cyclic iron carbide formation and decomposition mechanism enhances methane decomposition and carbon removal.

Conclusions:

  • Controlled oxidant addition to methane pyrolysis is a viable strategy to enhance hydrogen and carbon production.
  • This method effectively mitigates catalyst deactivation and carbon buildup, improving process economics.
  • The findings are applicable to Fe, Ni, and Co-based catalysts, broadening potential industrial implementation.