When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Lead (IV) acetate - Wikipedia

    en.wikipedia.org/wiki/Lead(IV)_acetate

    Lead(IV) acetate or lead tetraacetate is an metalorganic compound with chemical formula Pb(C 2 H 3 O 2) 4. It is a colorless solid that is soluble in nonpolar, organic solvents, indicating that it is not a salt. It is degraded by moisture and is typically stored with additional acetic acid. The compound is used in organic synthesis. [2]

  3. Criegee oxidation - Wikipedia

    en.wikipedia.org/wiki/Criegee_oxidation

    The Criegee oxidation is a glycol cleavage reaction in which vicinal diols are oxidized to form ketones and aldehydes using lead tetraacetate. It is analogous to the use of periodate (Malaprade reaction) but uses a milder oxidant. This oxidation was discovered by Rudolf Criegee and coworkers and first reported in 1931 using ethylene glycol as ...

  4. Glycol cleavage - Wikipedia

    en.wikipedia.org/wiki/Glycol_cleavage

    Glycol cleavage is a specific type of organic chemistry oxidation. The carbon–carbon bond in a vicinal diol (glycol) is cleaved and instead the two oxygen atoms become double-bonded to their respective carbon atoms. Depending on the substitution pattern in the diol, these carbonyls will be ketones and/or aldehydes. [1]

  5. 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.

  6. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    Sodium hypochlorite, [4] lead tetraacetate, [5] N-bromosuccinimide, and (bis(trifluoroacetoxy)iodo)benzene [6] can effect a Hofmann rearrangement. The intermediate isocyanate can be trapped with various nucleophiles to form stable carbamates or other products rather than undergoing decarboxylation.

  7. Autoxidation - Wikipedia

    en.wikipedia.org/wiki/Autoxidation

    Autoxidation is therefore a fairly broad term and can encompass examples of photooxygenation and catalytic oxidation. The common mechanism is a free radical chain reaction, where the addition of oxygen gives rise to hydroperoxides and their associated peroxy radicals (ROO•). [5]

  8. Rancidification - Wikipedia

    en.wikipedia.org/wiki/Rancidification

    The Rancimat method is carried out using an air current at temperatures between 50 and 220 °C. The volatile oxidation products (largely formic acid [14]) are carried by the air current into the measuring vessel, where they are absorbed (dissolve) in the measuring fluid (distilled water). By continuous measurement of the conductivity of this ...

  9. Lead compounds - Wikipedia

    en.wikipedia.org/wiki/Lead_compounds

    Lead(II) oxide is also soluble in alkali hydroxide solutions to form the corresponding plumbite salt. [2] PbO + 2 OH − + H 2 O → Pb(OH) 2− 4. Chlorination of plumbite solutions causes the formation of lead's +4 oxidation state. Pb(OH) 2− 4 + Cl 2 → PbO 2 + 2 Cl − + 2 H 2 O. Lead dioxide is representative of the +4 oxidation state ...

  1. Related searches lead tetraacetate oxidation mechanism of formation of alcohol in air flow

    oxidation of primary alcoholwhat is oxidation in alcohol
    how does alcohol oxidation work