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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.
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.
The hydroxide ion is intermediate in nucleophilicity between the fluoride ion F −, and the amide ion NH − 2. [51] Ester hydrolysis under alkaline conditions (also known as base hydrolysis) R 1 C(O)OR 2 + OH − ⇌ R 1 CO(O)H + − OR 2 ⇌ R 1 CO 2 − + HOR 2. is an example of a hydroxide ion serving as a nucleophile. [52]
The hydroxyl radical, Lewis structure shown, contains one unpaired electron. Lewis dot structure of a Hydroxide ion compared to a hydroxyl radical. In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron.
A: hydroxyl radical (HO •); B: hydroxide ion (HO −); C: singlet oxygen (1 O 2); D: superoxide anion (O 2 •−); E: peroxide ion (O 2− 2); F: hydrogen peroxide (H 2 O 2); G: nitric oxide (NO •) In chemistry and biology, reactive oxygen species (ROS) are highly reactive chemicals formed from diatomic oxygen (O 2), water, and hydrogen ...
The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pK a is usually between 10 and 12). Deprotonation of a phenol forms a corresponding negative phenolate ion or phenoxide ion , and the corresponding salts are called phenolates or phenoxides ( aryloxides according ...
In chemistry, hydroxylation refers to the installation of a hydroxyl group (−OH) into an organic compound. Hydroxylations generate alcohols and phenols, which are very common functional groups. Hydroxylation confers some degree of water-solubility. Hydroxylation of a hydrocarbon is an oxidation, thus a step in degradation.
In o-hydroxy compounds, when the hydroxyl group is protonated, an intramolecular hydrogen bond can form between the hydroxyl hydrogen and the carbonyl oxygen, stabilizing a resonance structure with positive charge on the carbonyl carbon, thus increasing the carbonyl carbon's electrophilicity (7).