enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Redox - Wikipedia

    en.wikipedia.org/wiki/Redox

    Example of a reduction–oxidation reaction between sodium and chlorine, with the OIL RIG mnemonic [1] Redox (/ ˈ r ɛ d ɒ k s / RED-oks, / ˈ r iː d ɒ k s / REE-doks, reduction–oxidation [2] or oxidation–reduction [3]: 150 ) is a type of chemical reaction in which the oxidation states of the reactants change. [4]

  3. Oxidizing agent - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_agent

    Example of a reduction–oxidation reaction between sodium and chlorine, with the OIL RIG mnemonic [1] Tetracyanoquinodimethane is an organic electron-acceptor. Electron acceptors participate in electron-transfer reactions. In this context, the oxidizing agent is called an electron acceptor and the reducing agent is called an electron donor.

  4. Reducing agent - Wikipedia

    en.wikipedia.org/wiki/Reducing_agent

    In the above equation, the Iron (Fe) has an oxidation number of 0 before and 3+ after the reaction. For oxygen (O) the oxidation number began as 0 and decreased to 2−. These changes can be viewed as two "half-reactions" that occur concurrently: Oxidation half reaction: Fe 0 → Fe 3+ + 3e −; Reduction half reaction: O 2 + 4e − → 2 O 2−

  5. Photooxygenation - Wikipedia

    en.wikipedia.org/wiki/Photooxygenation

    The Schenck ene reaction is an example of a Type II photooxygenation. A photooxygenation is a light-induced oxidation reaction in which molecular oxygen is incorporated into the product(s). [ 1 ] [ 2 ] Initial research interest in photooxygenation reactions arose from Oscar Raab's observations in 1900 that the combination of light, oxygen and ...

  6. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  7. Dakin oxidation - Wikipedia

    en.wikipedia.org/wiki/Dakin_oxidation

    The Dakin oxidation. The Dakin oxidation (or Dakin reaction) is an organic redox reaction in which an ortho- or para-hydroxylated phenyl aldehyde (2-hydroxybenzaldehyde or 4-hydroxybenzaldehyde) or ketone reacts with hydrogen peroxide (H 2 O 2) in base to form a benzenediol and a carboxylate. Overall, the carbonyl group is oxidised, whereas the ...

  8. Organic redox reaction - Wikipedia

    en.wikipedia.org/wiki/Organic_redox_reaction

    Examples of organic reactions that can take place in an electrochemical cell are the Kolbe electrolysis. [3] In disproportionation reactions the reactant is both oxidised and reduced in the same chemical reaction forming two separate compounds. Asymmetric catalytic reductions and asymmetric catalytic oxidations are important in asymmetric ...

  9. Oxidase - Wikipedia

    en.wikipedia.org/wiki/Oxidase

    In reactions involving donation of a hydrogen atom, oxygen is reduced to water (H 2 O) or hydrogen peroxide (H 2 O 2). Some oxidation reactions, such as those involving monoamine oxidase or xanthine oxidase, typically do not involve free molecular oxygen. [1] [2] The oxidases are a subclass of the oxidoreductases. The use of dioxygen is the ...