Examples of pKa in the following topics:
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- The logarithmic constant (pKa) is equal to -log10(Ka).
- The larger the value of pKa, the smaller the extent of dissociation.
- A weak acid has a pKa value in the approximate range of -2 to 12 in water.
- Acids with a pKa value of less than about -2 are said to be strong acids.
- What is the pKa for acetic acid?
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- More precisely, the acid must be stronger in aqueous solution than a hydronium ion (H+), so strong acids have a pKa < -1.74.
- An example is hydrochloric acid (HCl), whose pKa is -6.3.
- p-Toluenesulfonic acid is an example of an organic soluble strong acid, with a pKa of -2.8.
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- The Henderson–Hasselbalch equation connects the measurable value of the pH of a solution with the theoretical value pKa.
- The Henderson–Hasselbalch equation mathematically connects the measurable pH of a solution with the pKa (which is equal to -log Ka) of the acid.
- The equation can be derived from the formula of pKa for a weak acid or buffer.
- With a given pH and known pKa, the solution of the Henderson-Hasselbalch equation gives the logarithm of a ratio which can be solved by performing the antilogarithm of pH/pKa:
- What is the pH of a buffer solution consisting of 0.0350 M NH3 and 0.0500 M NH4+ (Ka for NH4+ is 5.6 x 10-10)?
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- The logarithmic constant, pKa, which is equal to −log10 (Ka), is sometimes incorrectly referred to as an acid dissociation constant as well.
- Smaller Ka values yield larger pKa values.
- Therefore, the larger the value of pKa, the smaller the extent of dissociation.
- A weak acid has a pKa value in the approximate range of -2 to 12 in water.
- A pH indicator is a weak acid or weak base that changes color in the transition pH range, which is approximately pKa ± 1.
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- These acids can be arranged in order of their pKa values and, by extension, their relative strengths:
- HOCl pKa = 7.5 < HOBr pKa = 8.6 < HOI pKa = 10.6
- Recall that smaller values of pKa correspond to greater acid strength.
- Consider the family of chlorooxoacids, which are arranged below in order of pKa values:
- HOClO3 pKa = -8 < HOClO2 pKa = -1.0 < HOClO pKa = 1.92 < HOCl pKa = 7.53
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- In the following table, pKa again refers to the conjugate acid of the base drawn above it.
- Its basicity and nucleophilicity may be modified by steric hindrance, as in the case of 2,6-dimethylpyridine (pKa=6.7), or resonance stabilization, as in the case of 4-dimethylaminopyridine (pKa=9.7).
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- Basicity may be related to the pKa of the corresponding conjugate acid, as shown below.
- Learning the pKa values for common compounds provides a useful foundation on which to build an understanding of acid-base factors in reaction mechanisms.
- Thus, 2,2,2-trifluroethoxide (pKa 12) is a weaker base and nucleophile than ethoxide (pKa 16).
- Two common examples of this exception, called the alpha effect, are hydroxide ion (pKa 15.7) compared with hydroperoxide ion (pKa 11.6), and ammonia (pKa 9.3) compared with hydrazine (pKa 8.0).
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- This delocalization substantially reduces the basicity of these compounds (pKa ca. –1) compared with amines (pKa ca. 11).
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- The acid strength increases as the experimental pKa values decrease in the following order:
- HF (pKa = 3.1) < HCl (pKa = -6.0) < HBr (pKa = -9.0) < HI (pKa = -9.5).
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- Stronger acids have smaller or more negative pKa values than do weaker acids.
- If the pH is lowered by two or more units relative to the pKa, the acid concentration will be greater than 99%.
- On the other hand, if the pH (relative to pKa) is raised by two or more units the conjugate base concentration will be over 99%.
- A useful rule here is: pKa + pKb = 14.
- A useful table of pKa values in DMSO solution has been compiled from the work of F.G.