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On the other hand, if a chemical is a weak acid its conjugate base will not necessarily be strong. Consider that ethanoate, the conjugate base of ethanoic acid, has a base splitting constant (Kb) of about 5.6 × 10 −10, making it a weak base. In order for a species to have a strong conjugate base it has to be a very weak acid, like water.
The sulfate ion carries an overall charge of −2 and it is the conjugate base of the bisulfate (or hydrogensulfate) ion, HSO − 4, which is in turn the conjugate base of H 2 SO 4, sulfuric acid. Organic sulfate esters, such as dimethyl sulfate, are covalent compounds and esters of sulfuric acid.
Speciation of ions refers to the changing concentration of varying forms of an ion as the pH of the solution changes. [1]The ratio of acid, AH and conjugate base, A −, concentrations varies as the difference between the pH and the pK a varies, in accordance with the Henderson-Hasselbalch equation.
In chemistry and biochemistry, the Henderson–Hasselbalch equation = + ([] []) relates the pH of a chemical solution of a weak acid to the numerical value of the acid dissociation constant, K a, of acid and the ratio of the concentrations, [] [] of the acid and its conjugate base in an equilibrium.
Biosynthesis of sulfate esters requires an activated sulfate donor, usually adenosine 5'-phosphosulfate (APS) or 3'-phosphoadenosine-5'-phosphosulfate (PAPS). [2] Sulfate esters may be hydrolyzed by sulfatase enzyme to release the parent alcohol and a sulfate ion. [3] Steroid sulfation is one of the most common of all forms of steroid conjugation.
Some bonding modes in complexes of the sulfate ligand. Transition metal sulfate complexes or sulfato complexes are coordination complexes with one or more sulfate ligands. Being the conjugate base of a strong acid (sulfuric acid), sulfate is not basic. It is more commonly a counterion in coordination chemistry, not a ligand.
In chemistry, protonation (or hydronation) is the adding of a proton (or hydron, or hydrogen cation), usually denoted by H +, to an atom, molecule, or ion, forming a conjugate acid. [1] (The complementary process, when a proton is removed from a Brønsted–Lowry acid, is deprotonation.) Some examples include The protonation of water by ...
In coordination chemistry, the S N 1cB (conjugate base) mechanism describes the pathway by which many metal amine complexes undergo substitution, that is, ligand exchange. Typically, the reaction entails reaction of a polyamino metal halide with aqueous base to give the corresponding polyamine metal hydroxide: [1]