Search results
Results From The WOW.Com Content Network
Long chain oxo-alcohols are often prepared using alpha-olefins from the Shell higher olefin process, to give secondary alcohols such as isodecyl alcohol. [2] Key oxo alcohols that are sold in commerce include the following: 2-Methyl-2-butanol (2M2B) n-Butanol; 2-Ethylhexanol; 2-Propylheptanol; Isononyl alcohol; Isodecyl alcohol
2-Methyl-1-butanol (IUPAC name, also called active amyl alcohol) is an organic compound with the formula CH 3 CH 2 CH(CH 3)CH 2 OH. It is one of several isomers of amyl alcohol.This colorless liquid occurs naturally in trace amounts and has attracted some attention as a potential biofuel, exploiting its hydrophobic (gasoline-like) and branched structure.
[2] Through a variety of mechanisms, the removal of a hydride equivalent converts a primary or secondary alcohol to an aldehyde or ketone, respectively. The oxidation of primary alcohols to carboxylic acids normally proceeds via the corresponding aldehyde, which is transformed via an aldehyde hydrate (gem-diol, R-CH(OH) 2) by reaction with ...
Proton transfer from the oxonium ion to a second molecule of the alcohol gives an activated complex; Protonation of one of the hydroxy groups of the activated complex gives a new oxonium ion. Loss of water from this oxonium ion and subsequent deprotonation gives the ester. A generic mechanism for an acid Fischer esterification is shown below.
3-Methyl-2-butanol, an organic chemical compound used as a solvent and an intermediate Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.
Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).
Use of NaBH 4 can give any of these results, but InCl 3 or NiCl 2 catalyze specifically 1,4‑reductions. [1] Potassium or lithium tri(sec‑butyl)borohydride sometimes selects 1,4‑reductions, but can be stymied by steric hindrance. [20] Triphenylphosphinocopper hydride clusters directs catalytic hydrogenation to perform specifically ...
Biolipid transesterification has also been recently shown by Japanese researchers to be possible using a supercritical methanol methodology, whereby high temperature, high-pressure vessels are used to physically catalyze the biolipid/methanol reaction into fatty-acid methyl esters.