2001
DOI: 10.1021/ed078p116
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The Strength of the Hydrohalic Acids

Abstract: This article brings to mind that the textbook acidity constants of the hydrohalic acids (except for HF) are erroneous because of outmoded conjectures about the HX solubilities. Here we invoke theoretical calculations of HX solubilities based on current solvation models. Although we do not claim to have provided the ultimate answer, it is safe to assume that the solubilities of both HCl and HBr are much higher than commonly surmised.

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Cited by 14 publications
(8 citation statements)
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“…Hydrohalic acids are considered strong acids, while HCl is defined as a strong acid and both HBr and HI are defined as very strong acids. This is according to few factors including the free energy of bond breaking and hydration. , Accordingly, one would expect that HI and HBr will have a stronger shortening effect relative to HCl. This forecast does not necessarily fit the observations because the use of different concentrations of the acids and examining the shortening effect of each acid separately.…”
Section: Resultsmentioning
confidence: 99%
“…Hydrohalic acids are considered strong acids, while HCl is defined as a strong acid and both HBr and HI are defined as very strong acids. This is according to few factors including the free energy of bond breaking and hydration. , Accordingly, one would expect that HI and HBr will have a stronger shortening effect relative to HCl. This forecast does not necessarily fit the observations because the use of different concentrations of the acids and examining the shortening effect of each acid separately.…”
Section: Resultsmentioning
confidence: 99%
“…12,13 Details of energy minimization using 3D-RISM, MD simulation setup, and NLPB calculations are give in the Supporting Information. [7][8][9][10] Molecular Mechanics Force Fields.…”
Section: Discussionmentioning
confidence: 99%
“…HCl, for example, has been reported to have a pK a ranging from -3 to -7, HBr from -4 to -9, and HNO 3 from -1 to -2. [20][21][22][23][24] The addition of ethanol and silane to the sol will also increase the pK a , 20,24 thus making it difficult to compare actual numbers. For HNO 3 , the pK a in ethanol is estimated to be ca.…”
Section: Discussionmentioning
confidence: 99%