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Propane-2,2-diol, an example of a geminal diol. A geminal diol has two hydroxyl groups bonded to the same atom. These species arise by hydration of the carbonyl compounds. The hydration is usually unfavorable, but a notable exception is formaldehyde which, in water, exists in equilibrium with methanediol H 2 C(OH) 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 water ...
2-Methyl-2,4-pentanediol (MPD) is an organic compound with the formula (CH 3) 2 C(OH)CH 2 CH(OH)CH 3.This colourless liquid is a chiral diol.It is produced industrially from diacetone alcohol by hydrogenation. [4]
The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...
In the case of ethanol production, this step can be written: H 2 SO 4 + C 2 H 4 → C 2 H 5-O-SO 3 H. Subsequently, this sulphate ester is hydrolyzed to regenerate sulphuric acid and release ethanol: C 2 H 5-O-SO 3 H + H 2 O → H 2 SO 4 + C 2 H 5 OH. This two step route is called the "indirect process".
In cyclic systems, the reaction presents more features of interest. In these reactions, the stereochemistry of the diol plays a crucial role in deciding the major product. An alkyl group which is situated trans- to the leaving –OH group may migrate to the carbocation center, but cis- alkyl groups migrate at a very low rate.
A geminal diol (or gem-diol for short) is any organic compound having two hydroxyl functional groups (-O H) bound to the same carbon atom. Geminal diols are a subclass of the diols, which in turn are a special class of alcohols. Most of the geminal diols are considered unstable. The simplest geminal diol is methanediol CH 4 O 2 or H 2 C(OH) 2 ...
General structure of a halohydrin, where X = I, Br, F, or Cl Structure of the halohydrin 2-chloroethanol. In organic chemistry a halohydrin (also a haloalcohol or β-halo alcohol) is a functional group in which a halogen and a hydroxyl are bonded to adjacent carbon atoms, which otherwise bear only hydrogen or hydrocarbyl groups (e.g. 2-chloroethanol, 3-chloropropane-1,2-diol). [1]