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  2. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    The Cannizzaro reaction, named after its discoverer Stanislao Cannizzaro, is a chemical reaction which involves the base-induced disproportionation of two molecules of a non-enolizable aldehyde to give a primary alcohol and a carboxylic acid. [1] [2]

  3. 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 ...

  4. 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]

  5. 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]

  6. 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.

  7. 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, ...

  8. 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 .

  9. Having Trouble Finding Bleach? Here’s What To Use Instead - AOL

    www.aol.com/having-trouble-finding-bleach...

    Plus, because bleach is a cleaning agent, people tend to stock up on it to keep their home free of the coronavirus. So once bleach hits store shelves, it often leaves them just as quickly.