Weak base

In chemistry, a weak base is a chemical base that does not ionize fully in an aqueous solution. As Brønsted–Lowry bases 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 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:

$\mbox{pH} = -\log_{10} \left[ \mbox{H}^+ \right]$

Since bases are proton acceptors, the base receives a hydrogen ion from water, H₂O, and the remaining H⁺ concentration in the solution determines pH. Weak bases will have a higher H⁺ concentration because they are less completely protonated than stronger bases and, therefore, more hydrogen ions remain in the solution. If you plug in a higher H⁺ concentration into the formula, a low pH results. However, pH of bases is usually calculated using the OH⁻ concentration to find the pOH first. This is done because the H⁺ concentration is not a part of the reaction, while the OH⁻ concentration is.

$\mbox{pOH} = -\log_{10} \left[ \mbox{OH}^- \right]$

By multiplying a conjugate acid (such as NH₄⁺) and a conjugate base (such as NH₃) the following is given:

$K_a \times K_b = {[H_3O^+] [NH_3]\over[NH_4^+]} \times {[NH_4^+] [OH^-]\over[NH_3]} = [H_3O^+] [OH^-]$

Since ${K_w} = [H_3O^+] [OH^-]$ then, $K_a \times K_b = K_w$

By taking logarithms of both sides of the equation, the following is reached:

$logK_a + logK_b = logK_w$

Finally, multiplying throughout the equation by -1, the equation turns into:

$pK_a + pK_b = pK_w = 14.00$

After acquiring pOH from the previous pOH formula, pH can be calculated using the formula pH = pK_w - pOH where pK_w = 14.00.

Weak bases exist in chemical equilibrium much in the same way as weak acids do, with a base dissociation constant (K_b) indicating the strength of the base. For example, when ammonia is put in water, the following equilibrium is set up:

$\mathrm{K_b={[NH_4^+] [OH^-]\over[NH_3]}}$

Bases that have a large K_b will ionize more completely and are thus stronger bases. As stated above, pH of the solution depends on the H⁺ concentration, which is related to the OH⁻ concentration by the self-ionization constant (K_w = 1.0x10⁻¹⁴). A strong base has a lower H⁺ concentration because they are fully protonated and less hydrogen ions remain in the solution. A lower H⁺ concentration also means a higher OH⁻ concentration and therefore, a larger K_b.

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 K_b values become.

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.

The typical proton transfer equilibrium appears as such:

$B(aq) + H_2O(l) \leftrightarrow HB^+(aq) + OH^-(aq)$

B represents the base.

$Percentage\ protonated = {molarity\ of\ HB^+ \over\ initial\ molarity\ of\ B} \times 100\% = {[{HB}^+]\over [B]_{initial}} {\times 100\%}$

In this formula, [B]_initial is the initial molar concentration of the base, assuming that no protonation has occurred.

A typical pH problem

Calculate the pH and percentage protonation of a .20 M aqueous solution of pyridine, C₅H₅N. The K_b for C₅H₅N is 1.8 x 10⁻⁹.

First, write the proton transfer equilibrium:

$\mathrm{H_2O(l) + C_5H_5N(aq) \leftrightarrow C_5H_5NH^+ (aq) + OH^- (aq)}$

$K_b=\mathrm{[C_5H_5NH^+] [OH^-]\over [C_5H_5N]}$

The equilibrium table, with all concentrations in moles per liter, is

	C5H5N	C5H6N^+	OH^−
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	$K_b=\mathrm {1.8 \times 10^{-9}} = {x \times x \over .20-x}$
We can assume that x is so small that it will be meaningless by the time we use significant figures.	$\mathrm {1.8 \times 10^{-9}} \approx {x^2 \over .20}$
Solve for x.	$\mathrm x \approx \sqrt{.20 \times (1.8 \times 10^{-9})} = 1.9 \times 10^{-5}$
Check the assumption that x << .20	$\mathrm 1.9 \times 10^{-5} \ll .20$; so the approximation is valid
Find pOH from pOH = -log [OH^−] with [OH^−]=x	$\mathrm pOH \approx -log(1.9 \times 10^{-5}) = 4.7$
From pH = pKw - pOH,	$\mathrm pH \approx 14.00 - 4.7 = 9.3$
From the equation for percentage protonated with [HB^+] = x and [B]initial = .20,	$\mathrm percentage \ protonated = {1.9 \times 10^{-5} \over .20} \times 100\% = .0095\%$

This means .0095% of the pyridine is in the protonated form of C₅H₅NH⁺.

Examples

• Alanine,
• Ammonia, NH₃
• Methylamine, CH₃NH₂, C₅H₈O₂

Other weak bases are essentially any bases not on the list of strong bases.

Simple Facts

• 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.^[1]
• 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.^[2]

See also

• Strong base
• Weak acid

References

1. Atkins, Peter, and Loretta Jones. Chemical Principles: The Quest for Insight, 3rd Ed., New York: W.H. Freeman, 2005.
2. Clark, Jim. "Strong and Weak Bases."N.p.,2002. Web.

External links

• Explanation of strong and weak bases from ChemGuide
• Guide to Weak Bases from Georgetown course notes
• Article on Acidity of Solutions of Weak Bases from Intute