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#REDIRECT [[Acid strength#Strong acids]] |
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{{Acids and bases}} |
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A '''strong acid''' is an [[acid]] that [[Ionization|ionizes]] completely in an [[aqueous solution]] by losing one [[proton]], according to the equation |
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:HA(aq) → H<sup>+</sup>(aq) + A<sup>−</sup>(aq) |
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For [[sulfuric acid]] which is [[diprotic acid|diprotic]], the "strong acid" designation refers only to dissociation of the first proton |
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:H<sub>2</sub>SO<sub>4</sub>(aq) → H<sup>+</sup>(aq) + HSO<sub>4</sub><sup>−</sup>(aq) |
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More precisely, the acid must be stronger in aqueous solution than [[hydronium]] ion, so strong acids are acids with a [[acid dissociation constant|p''K''<sub>a</sub>]] < −1.74. An example is [[Hydrochloric acid|HCl]] for which pK<sub>a</sub> = -6.3.<ref name="Jolly"/> 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 substance|corrosive]], this is not always true. The [[carborane]] [[superacid]] H(CHB<sub>11</sub>Cl<sub>11</sub></sub>), which is one million times stronger than [[sulfuric acid]],<ref>George A. Olah, et. al. ''Superacid Chemistry'', 2nd ed., Wiley, p. 41.</ref><ref>That is, the ability of the carborane superacid to protonate a given base (B) is one million times greater than a solution of sulfuric acid, so that the ratio [BH<sup>+</sup>] / [B] is one million times higher. The relative acidities of strong acids can be evaluated using the [[Hammett acidity function]].</ref> is entirely non-corrosive, whereas the [[weak acid]] [[hydrofluoric acid]] (HF) is extremely corrosive and can dissolve, among other things, glass and all metals except [[iridium]]{{Citation needed|date=January 2010}}. |
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In all other acid-water reactions, 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 constant]]s of strong acids from all other acids is so small that this is a reasonable demarcation. |
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Due to the complete dissociation of strong acids in aqueous solution, the concentration of hydronium ions in the water is equal to the total concentration (ionized and un-ionized) of the acid introduced to solution: [H<sup>+</sup>] = [A<sup>−</sup>] = [HA]<sub>total</sub> and pH = −log[H<sup>+</sup>]. |
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==Determining acid strength== |
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The strength of an acid, in comparison to other acids, can be determined without the use of [[pH]] calculations by observing the following characteristics: |
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# '''Electronegativity''': The higher the [[electronegativity]] of a [[conjugate base]] in the same period, the more acidic. |
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# '''Atomic Radius''': With increasing atomic radius, acidity also increases. For example, HCl and HI, both strong acids, ionize 100% in water to become their respective ionic constituents. However, HI is stronger than HCl. This is because the atomic radius of an atom of iodine is much larger than that of a chlorine atom. As a result, the negative charge over the I<sup>-</sup> anion is dispersed over a larger electron cloud and its attraction for the proton (H<sup>+</sup>) is not as strong as the same attraction in HCl. Therefore, HI is ionized (deprotonated) more readily. |
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# '''Charge''': The more positively charged a species is, the more acidic (neutral molecules can be stripped of protons more easily than anions, and cations are more acidic than comparable molecules). |
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==Some common strong acids (as defined above)== |
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(Strongest to the weakest) |
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* [[Hydroiodic acid]] HI ([[acid dissociation constant|pK<sub>a</sub>]] = −9.3)<ref name="Jolly">William L. Jolly "Modern Inorganic Chemistry" (McGraw-Hill, 1984), p.177</ref> |
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* [[Hydrobromic acid]] HBr (pK<sub>a</sub> = −8.7)<ref name="Jolly"/> |
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* [[Perchloric acid]] HClO<sub>4</sub> (pK<sub>a</sub> ≈ −8)<ref name="Housecroft">{{Housecroft2nd|page=171}}</ref> |
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* [[Hydrochloric acid]] HCl (pK<sub>a</sub> = −6.3)<ref name="Jolly"/> |
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* [[Sulfuric acid]] H<sub>2</sub>SO<sub>4</sub> (first dissociation only, ''pK''<sub>a1</sub> ≈ −3)<ref name="Housecroft"/> |
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* [[p-Toluenesulfonic acid]] (pK<sub>a</sub> = −2.8) Organic soluble strong acid |
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== Almost strong acids == |
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These do not meet the strict criterion of being more acidic than H<sub>3</sub>O<sup>+</sup>, although in very dilute solution they dissociate almost completely, so sometimes they are included as "strong acids" |
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* [[Hydronium ion]] H<sub>3</sub>O<sup>+</sup> (pK<sub>a</sub> = -1.74). For purposes of simplicity, H<sub>3</sub>O<sup>+</sup> is often replaced in a chemical equation with H<sup>+</sup>. However, a bare proton does not exist free in water but instead is bound to one of the lone pairs of electrons on the H<sub>2</sub>O molecule. |
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* [[Nitric acid]] HNO<sub>3</sub> (pK<sub>a</sub> = -1.64)<ref name="Housecroft"/> |
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* [[Chloric acid]] HClO<sub>3</sub> (pK<sub>a</sub> = -1.0)<ref name="Housecroft"/> |
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* Some chemists include [[bromic acid]] (HBrO<sub>3</sub>){{Citation needed|date=June 2009}}, [[perbromic acid]] (HBrO<sub>4</sub>){{Citation needed|date=June 2009}}, [[iodic acid]] (HIO<sub>3</sub>){{Citation needed|date=June 2009}}, and [[periodic acid]] (HIO<sub>4</sub>){{Citation needed|date=June 2009}} as strong acids, although these are not universally accepted. |
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===Extremely strong acids (as protonators)=== |
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(Strongest to weakest) |
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* [[Fluoroantimonic acid]] H[SbF<sub>6</sub>] |
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* [[Magic acid]] FSO<sub>3</sub>HSbF<sub>5</sub> |
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* [[Carborane superacid]] H(CHB<sub>11</sub>Cl<sub>11</sub>) |
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* [[Fluorosulfuric acid]] FSO<sub>3</sub>H |
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* [[Triflic acid]] CF<sub>3</sub>SO<sub>3</sub>H |
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==References== |
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{{reflist}} |
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*Hill, John W., et al. "General Chemistry." 4th ed. New Jersey: Prentice Hall, 2005. |
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==External links== |
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* http://www.cm.utexas.edu/academic/courses/Spring2002/CH301/McDevitt/strong.htm |
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* http://jchemed.chem.wisc.edu/Journal/Issues/2000/Jul/abs849.html |
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* Titration of acids [http://www2.iq.usp.br/docente/gutz/Curtipot_.html - freeware for data analysis] and simulation of potentiometric [[titration curves]] |
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* Acids and Bases [http://www.sky-web.pwp.blueyonder.co.uk/Science/acids.htm - definitions] |
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[[Category:Acids]] |
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[[ar:حمض قوي]] |
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[[es:Ácido fuerte]] |
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[[fr:Acide fort]] |
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[[ko:강산]] |
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[[hr:Jake kiseline]] |
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[[it:Acido forte]] |
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[[he:חומצה חזקה]] |
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[[ht:Asid fò]] |
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[[ms:Asid kuat]] |
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[[nl:Sterk zuur]] |
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[[ja:強酸]] |
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[[pt:Ácido forte]] |
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[[simple:Strong acid]] |
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[[fi:Vahva happo]] |
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[[sv:Stark syra]] |
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[[zh:强酸]] |
Latest revision as of 00:46, 17 August 2018
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