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3) is a vital component of the pH buffering system [3] of the human body (maintaining acid–base homeostasis). 70%–75% of CO 2 in the body is converted into carbonic acid (H 2 CO 3), which is the conjugate acid of HCO − 3 and can quickly turn into it. [citation needed]
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 metabolic function. [1]
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.
Bjerrum plot of speciation for a hypothetical monoprotic acid: AH concentration as a function of the difference between pK and pH. Carbonic acid is the formal Brønsted–Lowry conjugate acid of the bicarbonate anion, stable in alkaline solution. The protonation constants have been measured to great precision, but depend on overall ionic ...
The HCO 3 − is a conjugate base that neutralizes acids, and the H + is a conjugate acid that neutralizes bases by Acid-base homeostasis. The HCO 3 − and H + are ideal for buffering pH in the blood and tissues because the pKa is close to the physiological pH = 7.2 – 7.6.
For alkaline buffers, a strong base such as sodium hydroxide may be added. Alternatively, a buffer mixture can be made from a mixture of an acid and its conjugate base. For example, an acetate buffer can be made from a mixture of acetic acid and sodium acetate. Similarly, an alkaline buffer can be made from a mixture of the base and its ...
It is the conjugate base of the hydrogencarbonate (bicarbonate) [8] ion, HCO − 3, which is the conjugate base of H 2 CO 3, carbonic acid. The Lewis structure of the carbonate ion has two (long) single bonds to negative oxygen atoms, and one short double bond to a neutral oxygen atom.
An acid may also form hydrogen bonds to its conjugate base. This process, known as homoconjugation, has the effect of enhancing the acidity of acids, lowering their effective pK a values, by stabilizing the conjugate base. Homoconjugation enhances the proton-donating power of toluenesulfonic acid in acetonitrile solution by a factor of nearly 800.