Weak base: Difference between revisions
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{{Short description|Tiffany Sullivan Airman 2}} |
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{{One source|date=April 2009}} |
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{{Acids and bases}} |
{{Acids and bases}} |
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A '''weak base''' is a [[base (chemistry)|base]] that, upon dissolution in water, does not [[Dissociation_(chemistry)|dissociate]] completely, so that the resulting aqueous solution contains only a small proportion of hydroxide ions and the concerned basic radical, and a large proportion of undissociated molecules of the base. |
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In chemistry, a '''weak base''' is a [[chemical]] [[base (chemistry)|base]] that does not [[ionize]] fully in an [[aqueous solution]]. As [[Brønsted–Lowry base]]s are proton acceptors, a weak base may also be defined as a chemical base in which [[protonation]] is incomplete. This results in a relatively low [[pH]] compared to [[Base (chemistry)#Strong bases|strong bases]]. Bases range from a pH of greater than 7 (7 is neutral, like pure water) to 14 (though some bases are greater than 14). pH has the formula: |
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==pH, K<sub>b</sub>, and K<sub>w</sub>== |
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Bases yield solutions in which the hydrogen ion [[Activity (chemistry)|activity]] is lower than it is in pure water, i.e., the solution is said to have a [[pH]] greater than 7.0 at standard conditions, potentially as high as 14 (and even greater than 14 for some bases). The formula for pH is: |
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:<math>\mbox{pH} = -\log_{10} \left[ \mbox{H}^+ \right]</math> |
:<math>\mbox{pH} = -\log_{10} \left[ \mbox{H}^+ \right]</math> |
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Bases are [[proton]] acceptors; a base will receive a hydrogen ion from water, H<sub>2</sub>O, and the remaining H<sup>+</sup> [[concentration]] in the solution determines pH. A weak base will have a higher H<sup>+</sup> concentration than a stronger base because it is less completely [[protonation|protonated]] than a stronger base and, therefore, more hydrogen ions remain in its solution. Given its greater H<sup>+</sup> concentration, the formula yields a lower pH value for the weak base. However, pH of bases is usually calculated in terms of the OH<sup>−</sup> concentration. This is done because the H<sup>+</sup> concentration is not a part of the reaction, whereas the OH<sup>−</sup> concentration is. The pOH is defined as: |
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:<math>\mbox{pOH} = -\log_{10} \left[ \mbox{OH}^- \right]</math> |
:<math>\mbox{pOH} = -\log_{10} \left[ \mbox{OH}^- \right]</math> |
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If we multiply the equilibrium constants of a [[conjugate acid]] (such as NH<sub>4</sub><sup>+</sup>) and a conjugate base (such as NH<sub>3</sub>) we obtain: |
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:<math> K_a \times K_b = {[H_3O^+] [NH_3]\over[NH_4^+]} \times {[NH_4^+] [OH^-]\over[NH_3]} = [H_3O^+] [OH^-]</math> |
:<math> K_a \times K_b = {[H_3O^+] [NH_3]\over[NH_4^+]} \times {[NH_4^+] [OH^-]\over[NH_3]} = [H_3O^+] [OH^-]</math> |
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As <math>{K_w} = [H_3O^+] [OH^-]</math> is just the [[self-ionization constant]] of water, we have '''''<math>K_a \times K_b = K_w</math>''''' |
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Taking the logarithm of both sides of the equation yields: |
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:<math>logK_a + logK_b = logK_w</math> |
:<math>logK_a + logK_b = logK_w</math> |
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Finally, multiplying |
Finally, multiplying both sides by -1, we obtain: |
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:<math>pK_a + pK_b = pK_w = 14.00</math> |
:<math>pK_a + pK_b = pK_w = 14.00</math> |
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With pOH obtained from the pOH formula given above, the pH of the base can then be calculated from <math>pH = pK_w - pOH</math>, where pK<sub>w</sub> = 14.00. |
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A weak base persists in [[chemical equilibrium]] in much the same way as a [[weak acid]] does, with a [[base dissociation constant]] ('''K<sub>b</sub>''') indicating the strength of the base. For example, when ammonia is put in water, the following equilibrium is set up: |
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:<math>\mathrm{K_b={[NH_4^+] [OH^-]\over[NH_3]}}</math> |
:<math>\mathrm{K_b={[NH_4^+] [OH^-]\over[NH_3]}}</math> |
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A base that has a large K<sub>b</sub> will ionize more completely and is thus a stronger base. As shown above, the pH of the solution, which depends on the H<sup>+</sup> concentration, increases with increasing OH<sup>−</sup> concentration; a greater OH<sup>−</sup> concentration means a smaller H<sup>+</sup> concentration, therefore a greater pH. Strong bases have smaller H<sup>+</sup> concentrations because they are more fully protonated, leaving fewer hydrogen ions in the solution. A ''smaller'' H<sup>+</sup> concentration means a ''greater'' OH<sup>−</sup> concentration and, therefore, a greater K<sub>b</sub> and a greater pH. |
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⚫ | NaOH (s) (sodium hydroxide) is a stronger base than (CH<sub>3</sub>CH<sub>2</sub>)<sub>2</sub>NH (l) ([[diethylamine]]) which is a stronger base than NH<sub>3</sub> (g) (ammonia). As the bases get weaker, the smaller the K<sub>b</sub> values become.<ref>{{cite web|url=http://www.chemguide.co.uk/physical/acidbaseeqia/bases.html|title=Explanation of strong and weak bases]|publisher=ChemGuide|access-date=2018-03-23}}</ref> |
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<!-- Image with unknown copyright status removed: [[Image: basestrength.jpg]] --> |
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<!-- The pie-chart representation is as follows: |
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⚫ | |||
* purple areas represent the fraction of OH- ions formed |
* purple areas represent the fraction of OH- ions formed |
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* red areas represent the cation remaining after ionization |
* red areas represent the cation remaining after ionization |
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==Percentage protonated== |
==Percentage protonated== |
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As seen above, the strength of a base depends primarily on pH. To help describe the strengths of weak bases, it is helpful to know the percentage protonated-the percentage of base molecules that have been protonated. A lower percentage will correspond with a lower pH because both numbers result from the amount of protonation. A weak base is less protonated, leading to a lower pH and a lower percentage protonated. |
As seen above, the strength of a base depends primarily on pH. To help describe the strengths of weak bases, it is helpful to know the percentage protonated-the percentage of base molecules that have been protonated. A lower percentage will correspond with a lower pH because both numbers result from the amount of protonation. A weak base is less protonated, leading to a lower pH and a lower percentage protonated.<ref name="Maskill1985">{{cite book|author=Howard Maskill|title=The physical basis of organic chemistry|url=https://books.google.com/books?id=4AXwAAAAMAAJ|year=1985|publisher=Oxford University Press, Incorporated|isbn=978-0-19-855192-8}}</ref> |
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The typical proton transfer equilibrium appears as such: |
The typical proton transfer equilibrium appears as such: |
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==A typical pH problem== |
==A typical pH problem== |
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Calculate the pH and percentage protonation of a .20 M aqueous solution of pyridine, C<sub>5</sub>H<sub>5</sub>N. The K<sub>b</sub> for C<sub>5</sub>H<sub>5</sub>N is 1.8 x 10<sup>−9</sup>. |
Calculate the pH and percentage protonation of a .20 M aqueous solution of pyridine, C<sub>5</sub>H<sub>5</sub>N. The K<sub>b</sub> for C<sub>5</sub>H<sub>5</sub>N is 1.8 x 10<sup>−9</sup>.<ref>{{cite web|url=http://www.kentchemistry.com/links/AcidsBases/pHWeakBases.htm|title=Calculations of weak bases|publisher=Mr Kent's Chemistry Page|access-date=2018-03-23}}</ref> |
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First, write the proton transfer equilibrium: |
First, write the proton transfer equilibrium: |
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==Examples== |
==Examples== |
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* [[Alanine]] |
* [[Alanine]] |
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* [[Ammonia]], NH<sub>3</sub> |
* [[Ammonia]], NH<sub>3</sub> |
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* [[Methylamine]], CH<sub>3</sub>NH<sub>2</sub> |
* [[Methylamine]], CH<sub>3</sub>NH<sub>2</sub> |
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* [[Ammonium hydroxide]], NH<sub>4</sub>OH |
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Other weak bases are essentially any bases not on the list of [[strong base]]s. |
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==Simple Facts== |
==Simple Facts== |
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*An example of a weak base is ammonia. It does not contain hydroxide ions, but it reacts with water to produce ammonium ions and hydroxide ions.<ref>Atkins, Peter, and Loretta Jones. Chemical Principles: The Quest for Insight, 3rd Ed., New York: W.H. Freeman, 2005.</ref> |
*An example of a weak base is ammonia. It does not contain hydroxide ions, but it reacts with water to produce ammonium ions and hydroxide ions.<ref>Atkins, Peter, and Loretta Jones. Chemical Principles: The Quest for Insight, 3rd Ed., New York: W.H. Freeman, 2005.</ref> |
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*The position of equilibrium varies from base to base when a weak base reacts with water. The further to the left it is, the weaker the base.<ref>Clark, Jim. "Strong and Weak Bases."N.p.,2002. Web.</ref> |
*The position of equilibrium varies from base to base when a weak base reacts with water. The further to the left it is, the weaker the base.<ref>Clark, Jim. "Strong and Weak Bases."N.p.,2002. Web.</ref> |
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*When there is a hydrogen ion gradient between two sides of the biological membrane, the concentration of some weak bases are focused on only one side of the membrane.<ref name="ac.els-cdn.com">{{Cite journal |doi = 10.1016/0002-9343(58)90376-0|title = Non-ionic diffusion and the excretion of weak acids and bases|journal = The American Journal of Medicine|volume = 24|issue = 5|pages = 709–729|year = 1958|last1 = Milne|first1 = M.D.|last2 = Scribner|first2 = B.H.|last3 = Crawford|first3 = M.A.}}</ref> Weak bases tend to build up in acidic fluids.<ref name="ac.els-cdn.com"/> Acid gastric contains a higher concentration of weak base than plasma.<ref name="ac.els-cdn.com"/> Acid urine, compared to alkaline urine, excretes weak bases at a faster rate.<ref name="ac.els-cdn.com"/> |
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==See also== |
==See also== |
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==External links== |
==External links== |
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* [http://www.chemguide.co.uk/physical/acidbaseeqia/bases.html Explanation of strong and weak bases] from ChemGuide |
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* [http://bouman.chem.georgetown.edu/S02/lect16/lect16.htm Guide to Weak Bases from Georgetown course notes] |
* [http://bouman.chem.georgetown.edu/S02/lect16/lect16.htm Guide to Weak Bases from Georgetown course notes] |
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* [http://www.intute.ac.uk/sciences/reference/plambeck/chem1/p01154.htm Article on Acidity of Solutions of Weak Bases] from Intute |
* [https://web.archive.org/web/20070926225948/http://www.intute.ac.uk/sciences/reference/plambeck/chem1/p01154.htm Article on Acidity of Solutions of Weak Bases] from Intute |
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[[Category:Bases]] |
[[Category:Bases (chemistry)]] |
Latest revision as of 22:26, 23 August 2024
A weak base is a base that, upon dissolution in water, does not dissociate completely, so that the resulting aqueous solution contains only a small proportion of hydroxide ions and the concerned basic radical, and a large proportion of undissociated molecules of the base.
pH, Kb, and Kw
[edit]Bases yield solutions in which the hydrogen ion activity is lower than it is in pure water, i.e., the solution is said to have a pH greater than 7.0 at standard conditions, potentially as high as 14 (and even greater than 14 for some bases). The formula for pH is:
Bases are proton acceptors; a base will receive a hydrogen ion from water, H2O, and the remaining H+ concentration in the solution determines pH. A weak base will have a higher H+ concentration than a stronger base because it is less completely protonated than a stronger base and, therefore, more hydrogen ions remain in its solution. Given its greater H+ concentration, the formula yields a lower pH value for the weak base. However, pH of bases is usually calculated in terms of the OH− concentration. This is done because the H+ concentration is not a part of the reaction, whereas the OH− concentration is. The pOH is defined as:
If we multiply the equilibrium constants of a conjugate acid (such as NH4+) and a conjugate base (such as NH3) we obtain:
As is just the self-ionization constant of water, we have
Taking the logarithm of both sides of the equation yields:
Finally, multiplying both sides by -1, we obtain:
With pOH obtained from the pOH formula given above, the pH of the base can then be calculated from , where pKw = 14.00.
A weak base persists in chemical equilibrium in much the same way as a weak acid does, with a base dissociation constant (Kb) indicating the strength of the base. For example, when ammonia is put in water, the following equilibrium is set up:
A base that has a large Kb will ionize more completely and is thus a stronger base. As shown above, the pH of the solution, which depends on the H+ concentration, increases with increasing OH− concentration; a greater OH− concentration means a smaller H+ concentration, therefore a greater pH. Strong bases have smaller H+ concentrations because they are more fully protonated, leaving fewer hydrogen ions in the solution. A smaller H+ concentration means a greater OH− concentration and, therefore, a greater Kb and a greater pH.
NaOH (s) (sodium hydroxide) is a stronger base than (CH3CH2)2NH (l) (diethylamine) which is a stronger base than NH3 (g) (ammonia). As the bases get weaker, the smaller the Kb values become.[1]
Percentage protonated
[edit]As seen above, the strength of a base depends primarily on pH. To help describe the strengths of weak bases, it is helpful to know the percentage protonated-the percentage of base molecules that have been protonated. A lower percentage will correspond with a lower pH because both numbers result from the amount of protonation. A weak base is less protonated, leading to a lower pH and a lower percentage protonated.[2]
The typical proton transfer equilibrium appears as such:
B represents the base.
In this formula, [B]initial is the initial molar concentration of the base, assuming that no protonation has occurred.
A typical pH problem
[edit]Calculate the pH and percentage protonation of a .20 M aqueous solution of pyridine, C5H5N. The Kb for C5H5N is 1.8 x 10−9.[3]
First, write the proton transfer equilibrium:
The equilibrium table, with all concentrations in moles per liter, is
C5H5N | C5H6N+ | OH− | |
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initial normality | .20 | 0 | 0 |
change in normality | -x | +x | +x |
equilibrium normality | .20 -x | x | x |
Substitute the equilibrium molarities into the basicity constant | |
We can assume that x is so small that it will be meaningless by the time we use significant figures. | |
Solve for x. | |
Check the assumption that x << .20 | ; so the approximation is valid |
Find pOH from pOH = -log [OH−] with [OH−]=x | |
From pH = pKw - pOH, | |
From the equation for percentage protonated with [HB+] = x and [B]initial = .20, |
This means .0095% of the pyridine is in the protonated form of C5H5NH+.
Examples
[edit]- Alanine
- Ammonia, NH3
- Methylamine, CH3NH2
- Ammonium hydroxide, NH4OH
Simple Facts
[edit]- An example of a weak base is ammonia. It does not contain hydroxide ions, but it reacts with water to produce ammonium ions and hydroxide ions.[4]
- The position of equilibrium varies from base to base when a weak base reacts with water. The further to the left it is, the weaker the base.[5]
- When there is a hydrogen ion gradient between two sides of the biological membrane, the concentration of some weak bases are focused on only one side of the membrane.[6] Weak bases tend to build up in acidic fluids.[6] Acid gastric contains a higher concentration of weak base than plasma.[6] Acid urine, compared to alkaline urine, excretes weak bases at a faster rate.[6]
See also
[edit]References
[edit]- ^ "Explanation of strong and weak bases]". ChemGuide. Retrieved 2018-03-23.
- ^ Howard Maskill (1985). The physical basis of organic chemistry. Oxford University Press, Incorporated. ISBN 978-0-19-855192-8.
- ^ "Calculations of weak bases". Mr Kent's Chemistry Page. Retrieved 2018-03-23.
- ^ Atkins, Peter, and Loretta Jones. Chemical Principles: The Quest for Insight, 3rd Ed., New York: W.H. Freeman, 2005.
- ^ Clark, Jim. "Strong and Weak Bases."N.p.,2002. Web.
- ^ a b c d Milne, M.D.; Scribner, B.H.; Crawford, M.A. (1958). "Non-ionic diffusion and the excretion of weak acids and bases". The American Journal of Medicine. 24 (5): 709–729. doi:10.1016/0002-9343(58)90376-0.