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  2. Kharasch–Sosnovsky reaction - Wikipedia

    en.wikipedia.org/wiki/Kharasch–Sosnovsky_reaction

    The Kharasch–Sosnovsky reaction is a method that involves using a copper or cobalt salt as a catalyst to oxidize olefins at the allylic position, subsequently condensing a peroxy ester (e.g. tert-Butyl peroxybenzoate) or a peroxide resulting in the formation of allylic benzoates or alcohols via radical oxidation. [1]

  3. Riley oxidation - Wikipedia

    en.wikipedia.org/wiki/Riley_oxidation

    The Riley Oxidation is amenable to a variety of carbonyl and olefinic systems with a high degree of regiocontrol based on the substitution pattern of the given system. Ketones with two available α-methylene positions react more quickly at the least hindered position.: [1] Allylic oxidation can be predicted by the substitution pattern on the ...

  4. Babler oxidation - Wikipedia

    en.wikipedia.org/wiki/Babler_oxidation

    Babler-Dauben oxidation of cyclic tertiary allylic alcohols. The reaction produces the desired enone product to high yield (typically >75%), is operationally simple and does not require air-free techniques or heating. [1] It suffers, however, from the very high toxicity and environmental hazard posed by the hexavalent chromium PCC oxidising ...

  5. Template:List of oxidation states of the elements - Wikipedia

    en.wikipedia.org/wiki/Template:List_of_oxidation...

    The oxidation states are also maintained in articles of the elements (of course), and systematically in the table {{Infobox element/symbol-to-oxidation-state}} See also [ edit ]

  6. Oxidation with chromium(VI) complexes - Wikipedia

    en.wikipedia.org/wiki/Oxidation_with_chromium(VI...

    Enones can be synthesized from tertiary allylic alcohols through the action of a variety of chromium(VI)-amine reagents, in a reaction known as the Babler oxidation. The reaction is driven by the formation of a more substituted double bond. (E)-Enones form in greater amounts than (Z) isomers because of chromium-mediated geometric isomerization ...

  7. Allyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Allyl_alcohol

    Allyl alcohols in general are prepared by allylic oxidation of allyl compounds, using selenium dioxide or organic peroxides. Other methods include carbon-carbon bond-forming reactions such as the Prins reaction, the Morita-Baylis-Hillman reaction, or a variant of the Ramberg-Bäcklund reaction. Hydrogenation of enones is another route.

  8. Element–reactant–product table - Wikipedia

    en.wikipedia.org/wiki/Element–reactant...

    An elementreaction–product table is used to find coefficients while balancing an equation representing a chemical reaction. Coefficients represent moles of a substance so that the number of atoms produced is equal to the number of atoms being reacted with. [1] This is the common setup: Element: all the elements that are in the reaction ...

  9. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    Reagents are "substances or compounds that are added to a system in order to bring about a chemical reaction or are added to see if a reaction occurs." [1] Some reagents are just a single element. However, most processes require reagents made of chemical compounds. Some of the most common ones used widely for specific reactive functions are ...

  1. Related searches allylic oxidation reagent reaction table of elements printable for kids

    allylic oxidationwhat is riley oxidation