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The latter is consistent with the pK a ’s of carbonic acid: pK 1 = 6.77 and pK 2 = 9.93. To a single metal ion, carbonate is observed to bind in both unidentate (κ 1-) and bidentate (κ 2-) fashions. [5] In the covalent bond classification method, κ 1-carbonate is anX ligand and κ 2-carbonate is an X 2 ligand.
It is isoelectronic with nitric acid HNO 3. The bicarbonate ion carries a negative one formal charge and is an amphiprotic species which has both acidic and basic properties. It is both the conjugate base of carbonic acid H 2 CO 3; and the conjugate acid of CO 2− 3, the carbonate ion, as shown by these equilibrium reactions: CO 2− 3 + 2 H 2 ...
Most of the carbonic acid then dissociates to bicarbonate and hydrogen ions. The bicarbonate buffer system is an acid-base homeostatic mechanism involving the balance of carbonic acid (H 2 CO 3), bicarbonate ion (HCO − 3), and carbon dioxide (CO 2) in order to maintain pH in the blood and duodenum, among other tissues, to support proper ...
An illustrative synthesis is the reaction of a cationic iron carbonyl with a stoichiometric amount of base: [2] [(C 5 H 5)(CO) 2 FeCO]BF 4 + NaOH → [(C 5 H 5)(CO) 2 FeCO 2 H + NaBF 4. When applied to simple metal carbonyls, this kind of conversion is sometimes called the Hieber base reaction. Decarboxylation of the resulting anion gives the ...
At ambient temperatures, pure carbonic acid is a stable gas. [6] There are two main methods to produce anhydrous carbonic acid: reaction of hydrogen chloride and potassium bicarbonate at 100 K in methanol and proton irradiation of pure solid carbon dioxide. [3] Chemically, it behaves as a diprotic Brønsted acid. [8] [9]
Another possibility is that only a portion of one molecule is transferred to the other molecule. This type of reaction occurs, for example, in redox and acid-base reactions. In redox reactions, the transferred particle is an electron, whereas in acid-base reactions it is a proton. This type of reaction is also called metathesis.
Attempts to prepare some carboxylate complexes, especially for electrophilic metals, often gives oxo derivatives. Examples include the oxo-acetates of Fe(III), Mn(III), and Cr(III). Pyrolysis of metal carboxylates affords acid anhydrides and the metal oxide. This reaction explains the formation of basic zinc acetate from anhydrous zinc diacetate.
Without the carbonic anhydrase catalyst, the reaction is very slow, however with the catalyst the reaction is 10 7 times faster. The reaction catalyzed by carbonic anhydrase is HCO − 3 + H + ⇌ CO 2 + H 2 O. Carbonic acid has a pK a of around 6.36 (the exact value depends on the medium), so at pH 7 a small percentage of the bicarbonate is ...