(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal hydrate (cas: 10030-85-0) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Category: alcohols-buliding-blocks
Identification of L-rhamnose in aspenwood was written by Jones, J. K. N.;Schoettler, J. R.. And the article was included in Tappi in 1952.Category: alcohols-buliding-blocks This article mentions the following:
Aspenwood (I) meal was hydrolyzed at 90° with N H2SO4; the hydrolyzate, when examined chromatographically showed the presence of xylose, galactose, and arabinose, and possibly glucose, mannose, and glucurone. L-Rhamnose (II) was present in very small amounts (< 1%), and was isolated as the cryst, hydrate, [α]D 9° (H2O), which was then converted into the characteristic benzoylhydrazone, m. 188°. Presumably this is the first time that II has been isolated from the hydrolyzate of I. In the experiment, the researchers used many compounds, for example, (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal hydrate (cas: 10030-85-0Category: alcohols-buliding-blocks).
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal hydrate (cas: 10030-85-0) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Category: alcohols-buliding-blocks
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts