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When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...
In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formula −OH and composed of one oxygen atom covalently bonded to one hydrogen atom. In organic chemistry , alcohols and carboxylic acids contain one or more hydroxy groups.
The term, "molecular model" refer to systems that contain one or more explicit atoms (although solvent atoms may be represented implicitly) and where nuclear structure is neglected. The electronic structure is often also omitted unless it is necessary in illustrating the function of the molecule being modeled.
11-Hydroxy-Δ 9-tetrahydrocannabinol (11-OH-Δ 9-THC, alternatively numbered as 7-OH-Δ 1-THC), usually referred to as 11-hydroxy-THC is the main active metabolite of tetrahydrocannabinol (THC), which is formed in the body after Δ 9-THC is consumed.
It consists of a methylene bridge (−CH 2 − unit) bonded to a hydroxyl group (−OH). This makes the hydroxymethyl group an alcohol . It has the identical chemical formula with the methoxy group ( −O−CH 3 ) that differs only in the attachment site and orientation to the rest of the molecule.
Hydroxylamine (also known as hydroxyammonia) is an inorganic compound with the chemical formula N H 2 OH.The compound exists as hygroscopic colorless crystals. [4] Hydroxylamine is almost always provided and used as an aqueous solution or more often as one of its salts such as hydroxylammonium sulfate, a water-soluble solid.
The OH groups still rotate even at room temperature around their symmetry axes and, therefore, cannot be detected by X-ray diffraction. [40] The room-temperature form of NaOH has the thallium iodide structure. LiOH, however, has a layered structure, made up of tetrahedral Li(OH) 4 and (OH)Li 4 units. [38]
Skeletal formulae of 1-hydroxy-2()-pyridinethione and its tautomer. The hydroxyl radical, • HO, is the neutral form of the hydroxide ion (HO –).Hydroxyl radicals are highly reactive and consequently short-lived; however, they form an important part of radical chemistry.