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  2. Oxidizing agent - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_agent

    The international pictogram for oxidizing chemicals. Dangerous goods label for oxidizing agents. An oxidizing agent (also known as an oxidant, oxidizer, electron recipient, or electron acceptor) is a substance in a redox chemical reaction that gains or "accepts"/"receives" an electron from a reducing agent (called the reductant, reducer, or electron donor).

  3. Reducing agent - Wikipedia

    en.wikipedia.org/wiki/Reducing_agent

    Reducing agents and oxidizing agents are the ones responsible for corrosion, which is the "degradation of metals as a result of electrochemical activity". [3] Corrosion requires an anode and cathode to take place. The anode is an element that loses electrons (reducing agent), thus oxidation always occurs in the anode, and the cathode is an ...

  4. Category:Oxidizing agents - Wikipedia

    en.wikipedia.org/wiki/Category:Oxidizing_agents

    Pages in category "Oxidizing agents" The following 195 pages are in this category, out of 195 total. This list may not reflect recent changes. ...

  5. Redox - Wikipedia

    en.wikipedia.org/wiki/Redox

    Thus, in the reaction, the reductant or reducing agent loses electrons and is oxidized, and the oxidant or oxidizing agent gains electrons and is reduced. The pair of an oxidizing and reducing agent that is involved in a particular reaction is called a redox pair. A redox couple is a reducing species and its corresponding oxidizing form, [7] e ...

  6. Tetrapropylammonium perruthenate - Wikipedia

    en.wikipedia.org/wiki/Tetrapropylammonium...

    Oxidation of alcohol to aldehyde with TPAP (0.06 eq.) and N-methylmorpholine N-oxide (1.7 eq.) with molecular sieves in dichloromethane. [1]Ruthenium tetroxide is a highly aggressive oxidant, but TPAP, which is its one-electron reduced derivative, is a mild oxidizing agent for the conversion of primary alcohols to aldehydes (the Ley oxidation). [2]

  7. 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.

  8. Pyridinium chlorochromate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chlorochromate

    PCC is used as an oxidant.In particular, it has proven to be highly effective in oxidizing primary and secondary alcohols to aldehydes and ketones, respectively.The reagent is more selective than the related Jones' Reagent, so there is little chance of over-oxidation to form carboxylic acids if acidified potassium permanganate is used as long as water is not present in the reaction mixture.

  9. Oxidizing acid - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_acid

    An oxidizing acid is a Brønsted acid that is a strong oxidizing agent. Most Brønsted acids can act as oxidizing agents, because the acidic proton can be reduced to hydrogen gas. Some acids contain other structures that act as stronger oxidizing agents than hydrogen ions. Generally, they contain oxygen in their anionic structure.