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Related Concept Videos

Carboxylic Acids to Methylesters: Alkylation using Diazomethane01:33

Carboxylic Acids to Methylesters: Alkylation using Diazomethane

2.3K
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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Hydroboration-Oxidation of Alkenes03:08

Hydroboration-Oxidation of Alkenes

8.7K
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
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Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

12.5K
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.
12.5K
Oxidation of Alcohols02:37

Oxidation of Alcohols

13.4K
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:
13.4K
Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration02:35

Ethers from Alkenes: Alcohol Addition and Alkoxymercuration-Demercuration

8.1K
Overview
Ethers can also be prepared from alkenes through acid-catalyzed addition of alcohols and alkoxymercuration–demercuration.
Preparation of Ethers by Acid-Catalyzed Addition of Alcohol to Alkenes
The acid-catalyzed addition of alcohol to an alkene involves treating the alkene with an excess of alcohol in the presence of an acid catalyst to form an ether under suitable conditions. The hydrogen will add to the less substituted carbon so that the nucleophile can attack the more...
8.1K
Oxymercuration-Reduction of Alkenes02:36

Oxymercuration-Reduction of Alkenes

7.8K
Oxymercuration–reduction of alkenes is one of the major reactions converting alkenes to alcohols. It involves the hydration of alkenes with mercuric acetate in a mixture of tetrahydrofuran and water, forming an organomercury adduct. This is followed by a demercuration step in which the adduct is reduced to an alcohol using sodium borohydride.
7.8K

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Visualizing Methane-Cycling Microbial Dynamics in Coastal Wetlands
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Visualizing Methane-Cycling Microbial Dynamics in Coastal Wetlands

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Methane Oxidation to Methanol.

Nicholas F Dummer1, David J Willock1, Qian He2

  • 1Max Planck-Cardiff Centre on the Fundamentals of Heterogeneous Catalysis FUNCAT, Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Main Building, Park Place, CardiffCF10 3AT, United Kingdom.

Chemical Reviews
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Summary
This summary is machine-generated.

Directly converting methane to methanol is difficult due to methane's low reactivity. This review explores catalytic routes and performance targets for scalable methanol production from methane.

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Area of Science:

  • Catalysis
  • Chemical Engineering
  • Sustainable Chemistry

Background:

  • Direct methane to methanol conversion presents significant scale-up challenges.
  • Low methane reactivity at recoverable conditions hinders efficient methanol synthesis.
  • Developing effective C-H activation routes is crucial for sustainable chemical production.

Purpose of the Study:

  • To review promising routes for direct methane to methanol conversion.
  • To evaluate performance targets essential for industrial-scale methanol production.
  • To provide a critical perspective on future operational developments.

Main Methods:

  • Examination of current methods and emerging heterogeneous catalysts.
  • Analysis of catalyst design, reaction mechanisms, and performance.
  • Review of initial gas-phase radical chemistry approaches and zeolite-based catalysts.

Main Results:

  • Gas-phase radical chemistry approaches faced limitations.
  • Zeolite-based catalysts (e.g., iron or copper containing) operate under milder conditions.
  • Key challenges include low methane conversion and product overoxidation.

Conclusions:

  • Despite challenges, interest in methane to methanol conversion remains high.
  • Effective C-H activation offers a pathway to valuable products from methane.
  • This reaction is vital for transitioning to net carbon zero using renewable methane.