Solubility of crystalline β-diols in water was written by Putnina, A.. And the article was included in Latvijas PSR Zinatnu Akademijas Vestis, Kimijas Serija in 1990.Name: 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:
Solubilities (weight per cent) of crystalline β-diols determined by refractometry at 25° are: 2-tert-butyl-1,3-propanediol 7.9; 2,2-diethyl-1,3-propanediol 4.68; 1-(3-bromophenyl)-2,2-dimethyl-1,3-propanediol 0.20; 1,3-decanediol 0.19; 1,3-dodecanediol 0.11; 2-ethyl-2-butyl-1,3-propanediol 1.4 weight%. Values determined by gas chromatog. are: 3-phenyl-2,2-dimethyl-1,3-propanediol 0.89; 2,2-dipropyl-1,3-propanediol 0.77; 2,2,5-trimethyl-1,3-hexanediol 0.58; 1-touyl-1-phenyl-1,3-propanediol 0.21; 2,2-diisobutyl-1,3-propanediol 0.056 weight%. An empirical equation for calculating β-diol solubility is proposed. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Name: 2-Butyl-2-ethylpropane-1,3-diol).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Name: 2-Butyl-2-ethylpropane-1,3-diol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts