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Related Concept Videos

Catalysis02:50

Catalysis

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The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
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Heterogeneous Catalysis01:22

Heterogeneous Catalysis

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Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...
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Predicting Reaction Outcomes02:24

Predicting Reaction Outcomes

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Kinetics describes the rate and path by which a reaction occurs. In contrast, thermodynamics deals with state functions and describes the properties, behavior, and components of a system. It is not concerned with the path taken by the process and cannot address the rate at which a reaction occurs. Although it does provide information about what can happen during a reaction process, it does not describe the detailed steps of what appears on an atomic or a molecular level. On the other hand,...
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Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation

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Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
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Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis01:13

Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis

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Hydrolysis of esters under acidic conditions proceeds through a nucleophilic acyl substitution. In the presence of excess water, the reaction proceeds in a reversible manner, forming carboxylic acids and alcohols.
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
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Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation01:28

Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation

6.3K
Unlike the easy catalytic hydrogenation of an alkene double bond, hydrogenation of a benzene double bond under similar reaction conditions does not take place easily. For example, in the reduction of stilbene, the benzene ring remains unaffected while the alkene bond gets reduced. Hydrogenation of an alkene double bond is exothermic and a favorable process. In contrast, to hydrogenate the first unsaturated bond of benzene, an energy input is needed; that is, the process is endothermic. This is...
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Achieving Moderate Pressures in Sealed Vessels Using Dry Ice As a Solid CO2 Source
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Carbocatalysis in Liquid-Phase Reactions.

Dang Sheng Su1, Guodong Wen1, Shuchang Wu2

  • 1Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang, 110016, China.

Angewandte Chemie (International Ed. in English)
|August 13, 2016
PubMed
Summary

Metal-free carbocatalysis offers a sustainable, "green" alternative for chemical transformations. This review critically analyzes carbocatalysts for liquid-phase reactions, focusing on mechanisms, advantages, and limitations.

Keywords:
active sitescarbocatalysisliquid phasenanocarbon materialsreaction mechanisms

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Area of Science:

  • Sustainable chemistry
  • Green chemistry
  • Catalysis

Background:

  • Metal-free catalysis is gaining traction for environmentally friendly chemical processes.
  • Carbocatalysis, utilizing carbon-based materials, presents a viable
  • green
  • alternative to traditional metal catalysts.
  • While established in gas-phase reactions, carbocatalysis for liquid-phase synthesis is an emerging field.

Approach:

  • This review critically analyzes the current state-of-the-art in carbocatalysis for liquid-phase reactions.
  • Focus is placed on elucidating the underlying reaction mechanisms.
  • Advantages and limitations of metal-free carbocatalysts are discussed.

Key Points:

  • Carbon-based materials demonstrate efficacy as alternatives to metal oxides in gas-phase dehydrogenation and selective oxidation.
  • Carbocatalysis is rapidly developing as a key technology for liquid-phase organic synthesis.
  • Understanding reaction mechanisms is crucial for optimizing carbocatalyst performance.

Conclusions:

  • Metal-free carbocatalysis is a promising avenue for sustainable organic synthesis.
  • Further research into mechanisms and catalyst design will enhance the utility of carbocatalysts.
  • Carbocatalysis offers significant advantages in terms of environmental impact and cost-effectiveness.