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  2. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    In photography, formaldehyde is used in low concentrations for the process C-41 (color negative film) stabilizer in the final wash step, [61] as well as in the process E-6 pre-bleach step, to make it unnecessary in the final wash. Due to improvements in dye coupler chemistry, more modern (2006 or later) E-6 and C-41 films do not need ...

  3. Neopentyl glycol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol

    Neopentyl glycol is synthesized industrially by the aldol reaction of formaldehyde and isobutyraldehyde. This creates the intermediate hydroxypivaldehyde, which can be converted to neopentyl glycol by either a Cannizzaro reaction with excess formaldehyde, or by hydrogenation using palladium on carbon. [2]

  4. Isobutyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Isobutyraldehyde

    In the context of butanol fuel, isobutyraldehyde is of interest as a precursor to isobutanol. E. coli as well as several other organisms has been genetically modified to produce isobutanol. α-Ketoisovalerate, derived from oxidative deamination of valine, is prone to decarboxylation to give isobutyraldehyde, which is susceptible to reduction to the alcohol: [3]

  5. Pentaerythritol - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol

    Pentaerythritol was first reported in 1891 by German chemist Bernhard Tollens and his student P. Wigand. [5] It may be prepared via a base-catalyzed multiple-addition reaction between acetaldehyde and 3 equivalents of formaldehyde to give pentaerythrose (CAS: 3818-32-4), followed by a Cannizzaro reaction with a fourth equivalent of formaldehyde to give the final product plus formate ion.

  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. Casiraghi formylation - Wikipedia

    en.wikipedia.org/wiki/Casiraghi_formylation

    The reaction requires a strong Brønsted base and a weak Lewis acid, and gives a methanol coproduct: [1] (H 2 CO) 2 n + n B + n LA + n HArOH → n HC(=O)ArOH + n [HB][LA:OMe] Formally, it combines the Cannizzaro disproportionation with a directed Friedel-Crafts acylation .

  8. A Fool Proof Guide to Safely Bleaching Your Hair at Home

    www.aol.com/bleach-hair-home-healthy-looking...

    To make your at-home bleach journey a bit easier, we’ve consulted a few experts to help you achieve healthy-looking blonde strands. Ahead, you’ll notice a 12-step bleaching process, ...

  9. Tishchenko reaction - Wikipedia

    en.wikipedia.org/wiki/Tishchenko_reaction

    The reaction is named after Russian organic chemist Vyacheslav Tishchenko, who discovered that aluminium alkoxides are effective catalysts for the reaction. [ 1 ] [ 2 ] [ 3 ] In the related Cannizzaro reaction , the base is sodium hydroxide and then the oxidation product is a carboxylic acid and the reduction product is an alcohol .