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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]
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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.
Predominance diagram: relates to equilibria involving polyoxyanions. pK a values are needed to construct these diagrams. Proton affinity : a measure of basicity in the gas phase. Stability constants of complexes : formation of a complex can often be seen as a competition between proton and metal ion for a ligand, which is the product of ...
The self-ionization of water (also autoionization of water, autoprotolysis of water, autodissociation of water, or simply dissociation of water) is an ionization reaction in pure water or in an aqueous solution, in which a water molecule, H 2 O, deprotonates (loses the nucleus of one of its hydrogen atoms) to become a hydroxide ion, OH −.
Dichloramine reacts with the hydroxide ion, which is always present in water, to yield nitroxyl and the chloride ion. [8] Alkali metals react with nitric oxide to give salts of the form MNO (M = metal). [9] However, generation of the (unstable) free acid from these salts is not entirely straightforward (see below).
Both the negatively charged anion HO −, called hydroxide, and the neutral radical HO·, known as the hydroxyl radical, consist of an unbonded hydroxy group. According to IUPAC definitions, the term hydroxyl refers to the hydroxyl radical (·OH) only, while the functional group −OH is called a hydroxy group. [1]
The free radicals generated by this process engage in secondary reactions. For example, the hydroxyl is a powerful, non-selective oxidant. [6] Oxidation of an organic compound by Fenton's reagent is rapid and exothermic and results in the oxidation of contaminants to primarily carbon dioxide and water.