Types of Acid or Base Reactions and pH Calculations Summary


1. Strong Acid Alone

HCl(g)H(aq)++Cl(aq)HCl_{(g)}\to H_{(aq)}^++Cl_{(aq)}^-

[H(aq)+]=[Cl(aq)]=[HCl](initial)[H_{(aq)}^+]=[Cl_{(aq)}^-]=[HCl]_{(initial)}

pH=log[H(aq)+]pH=-\log[H_{(aq)}^+]


2. Strong Base Alone

NaOHNa(aq)++OH(aq)NaOH\to Na_{(aq)}^++OH_{(aq)}^-

[OH(aq)]=[Na(aq)+]=[NaOH]initial[OH_{(aq)}^-]=[Na_{(aq)}^+]=[NaOH]_{initial}

pOH=log[OH(aq)]pOH=-\log[OH_{(aq)}^-]

pH=14pOHpH=14-pOH

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3. Weak Acid Alone

Example: 2.0 mols of weak acid, HA, with a Ka = 2 x 10-4 in 1.0 L of solution.
Step 1: Make an ICE table

HA(aq)+H2O(l)H3O(aq)++A(aq)HA_{(aq)}+H_2O_{(l)}\leftrightharpoons H_3O_{(aq)}^++A_{(aq)}^-

I2.0Mn/a00Cxn/a+x+xE2.0xn/axx\def\arraystretch{2}\begin{array}{c:c:c:c:c} I &2.0M &n/a &0 &0\\\hline C &-x &n/a &+x &+x\\ \hline E &2.0-x &n/a &x &x\end{array}

Step 2: Set up Ka equation and solve for [H3O+]

Ka=[H3O(aq)+][A(aq)][HA(aq)]=x22.0xx22.0Ka=\cfrac{[H_3O^+_{(aq)}][A^-_{(aq)}]}{[HA_{(aq)}]}=\cfrac{x^2}{2.0-x}\approx \cfrac{x^2}{2.0}
x=(2.0)Ka=0.02M=[H3O(aq)+]x=\sqrt{(2.0)K_a}=0.02M=[H_3O^+_{(aq)}]
pH=log[H3O(aq)+]=1.70pH=-\log [H_3O^+_{(aq)}]=1.70

4. Weak Base Alone

Example: 2.0 moles of weak base, B, with a Kb of 7 x 10-7 in 1.0 L of solution.
Step 1: Make an ICE table
B(aq)+H2O(l)OH(aq)+BH(aq)+B_{(aq)}+H_2O_{(l)}\leftrightharpoons OH_{(aq)}^-+BH_{(aq)}^+
I2.0Mn/a00Cxn/a+x+xE2.0xn/axx\def\arraystretch{2}\begin{array}{c:c:c:c:c} I &2.0M &n/a &0 &0\\\hline C &-x &n/a &+x &+x\\ \hline E &2.0-x &n/a &x &x\end{array}

Step 2: Set up Kb equation and solve for [OH- ]
Kb=[OH(aq)][BH(aq)+][B(aq)]=x22.0xx22.0K_b=\cfrac{[OH^-_{(aq)}][BH^+_{(aq)}]}{[B_{(aq)}]}=\cfrac{x^2}{2.0-x}\approx \cfrac{x^2}{2.0}
x=(2.0)Kb=0.00118M=[OH(aq)]x=\sqrt{(2.0)K_b}=0.00118M=[OH^-_{(aq)}]
pOH=log[OH(aq)]=2.93pOH=-\log [OH^-_{(aq)}]=2.93
pH=14pOH=11.07pH=14-pOH=11.07

When can we make a simplifying assumption about x?

In K= x2/(y-x)
When y/K > 400 you can simplify and ignore the "-x"

Important Relationships:

pH=log[H3O+] and [H3O+]=10pHpH=-\log⁡[H_3O^+]\ and\ [H_3O^+]=10^{-pH}

pOH=logOHand OH=10pOHpOH=-\log⁡OH^-and\ OH^-=10^{-pOH}


2H2OH3O++OH2H_2 O⇌H_3 O^++OH^-

In pure water, at 25 °C:
[H3O+]=[OH]=1.0×107M[H_3O^+]=[OH^-]=1.0\times10^{-7}M
Kw=[H3O+][OH]=1.0×1014 at 25°CK_w=[H_3O^+][OH^-]=1.0\times10^{-14}\ at\ 25°C
pH+pOH=pKw=14.00 at 25°CpH+pOH=pK_w=14.00\ at\ 25°C

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Ka is the acid dissociation constant and is defined as the equilibrium constant for the reaction below:

HA(aq)+H2O(l)A(aq)+H3O+(aq)HA(aq)+H_2O(l)⇌A^-(aq)+H_3O^+(aq)
Ka=[H3O+][A][HA]K_a=\cfrac{[H_3 O^+ ][A^- ]}{[HA]}
pKa=logKa and Ka=10pKapK_a=-\log⁡K_a\ and\ K_a=10^{-pK_a}

Strong acids dissociate completely.
HNO3(aq)H+(aq)+NO3(aq)HNO_3 (aq)→H^+ (aq)+NO_3^- (aq) (not an equilibrium, Ka is very large)

Weak acids partially dissociate to give H+ or H3O+
CH3COOH(aq)CH3COO(aq)+H+(aq)CH_3 COOH(aq)⇌CH_3 COO^- (aq)+H^+ (aq) (equilibrium, Ka)
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Kb is the base dissociation constant and is defined as the equilibrium constant for the reaction below:

B(aq)+H2O(l)BH+(aq)+OH(aq)B(aq)+H_2 O(l)⇌BH^+ (aq)+ OH^- (aq)
Kb=[BH+][OH][B]K_b=\cfrac{[BH^+ ][OH^- ]}{[B]}
pKb=logKb and Kb=10pKbpK_b=-\log⁡K_b\ and\ K_b=10^{-pK_b}
Strong bases dissociate completely.
LiOH(s)Li+(aq)+OH(aq)LiOH(s)→Li^+(aq)+OH^-(aq) (not an equilibrium, Kb is very large)

Weak bases partially dissociate (they accept protons to give OH-, but the reaction is not complete)

CH3NH2(aq)+H2O(l)CH3NH3+(aq)+OH(aq)CH_3NH_2(aq)+H_2O(l)⇌CH_3NH_3^+(aq)+OH^-(aq)

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For a given conjugate acid-base pair:

HA+H2OA+H3O+                   KaHA+H_2O⇌A^-+H_3O^+\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \color{red}{K_a}
A+H2OHA+OH                   Kb\underline{A^-+H_2O⇌HA+OH^-\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \color{red}{K_b}}
2H2OH3O++OH                      Kw2H_2 O⇌H_3 O^++OH^- \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \color{red} K_w
Ka×Kb=Kw=1×1014 and pKa+pKb=pKw=14.00 (at 25°C)K_a×K_b=K_w=1×10^{-14} \ and \ pK_a+pK_b=pK_w=14.00\ (at\ 25 °C)

Acid/Base Important Relationships Cheatsheet