Strong acid
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A strong acid is an acid that dissociates completely in an aqueous solution, or in other terms, with a pKa < -1.74, that of hydronium. This generally means that in aqueous solution at standard temperature and pressure, the concentration of hydronium ions is equal to the concentration of strong acid introduced to the solution. While strong acids are generally assumed to be the most corrosive, this is not always true. The carborane superacid (H(CHB11Cl11), which is one million times stronger than sulfuric acid, is entirely non-corrosive. The equation for complete dissociation of an acid in aqueous solution is as follows:
HA(aq) → H+(aq) + A-(aq)
In any other acid-water reaction, dissociation is not complete, so will be represented as an equilibrium, not a completed reaction. The typical definition of a weak acid is any acid that does not dissociate completely. The difference separating the acid dissociation constants of strong acids from all other acids is so great that this is a reasonable demarkation.
Due to the complete dissociation of strong acids in aqueous solution, the concentration of hydronium ions in the water is equal to the concentration of the acid introduced to solution: [HA] = [H+] = [A-] pH = -log[H+].
Some Common Strong Acids (As Ionisers)
(Strongest to weakest)
- Perchloric acid HClO4
- Hydroiodic acid HI
- Hydrobromic acid HBr
- Hydrochloric acid HCl
- Sulfuric acid H2SO4 (Ka1/first dissociation only)
- Nitric acid HNO3
- Hydronium ion H3O+
- Some chemists include chloric acid (HClO3), bromic acid (HBrO3), perbromic acid (HBrO4), iodic acid (HIO3), and periodic acid (HIO4) as strong acids, although these are not universally accepted.
Extremely Strong Acids (As Ionisers)
(Strongest to weakest)
- Fluoroantimonic acid HFSbF5
- Magic acid FSO3HSbF5
- Fluorosulfuric acid FSO3H
External links
- http://www.cm.utexas.edu/academic/courses/Spring2002/CH301/McDevitt/strong.htm
- http://jchemed.chem.wisc.edu/Journal/Issues/2000/Jul/abs849.html
- Titration of acids [- freeware for data analysis and simulation of potentiometric titration curves]
References
Hill, John W., et al. "General Chemistry." 4th ed. New Jersey: Prentice Hall, 2005.
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