20 - Monoprotic Acids & Bases - Chromedia [PDF]

Most acids/bases are considered weak - they do not dissociate fully in water. Only these select few dissociate fully and

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MONOPROTIC ACIDS & BASES CHEM 251 SDSU

ACIDS AND BASES acid is a proton donor - forms H3O+
 HA + H2O ⇌ A- + H3O+

• An

base is a proton acceptor - forms OH-
 B + H2O ⇌ BH+ + OH-

•A

• Vinegar: 


CH3CO2H + H2O ⇌ CH3CO2- + H3O+

• Ethylamine:


CH3CH2NH2 +H2O ⇌ CH3CH2NH3+ + OH2

PH = -log[H+] & pOH = -log[OH-]

• pH

• H 2O

⇌ H+ + OH-

• Kw =

1 × 10-14 = [H+]×[OH-]

• -log(Kw) = • 14

= pH + pOH

• HA •B

-log[H+] × -log[OH-]

+ H2O ⇌ H3O+ + A-

Ka = [H+][A-]/[HA]

+ H2O ⇌ BH+ + OH-

Kb = [BH+][OH-]/[B] 3

STRONG ACIDS AND BASES Most acids/bases are considered weak - they do not dissociate fully in water. Only these select few dissociate fully and are strong Strong Acids: HCl HBr HI H2SO4 HNO3 HClO4

Strong Bases: LiOH NaOH KOH RbOH CsOH R4NOH 4

“Not Weak” Bases: Mg(OH)2 Ca(OH)2 Sr(OH)2 Ba(OH)2

WEAK ACIDS AND BASES • All

weak acids and bases have dissociation constants, strong acids and bases do not have tabulated values.

• Weak

acids/bases do not dissociate fully in solution some HA or B remain.

• The

smaller the dissociation constant the weaker the acid/base - the closer the pH of the solution is to being 7.

5

ACID/BASE DISSOCIATION CALCULATIONS +

-



HA ⇌ H + A



The dissociation reactions always proceed stoichiometrically. So if one mole of HA dissociates, you get one + mole of H and one mole of A .



When doing calculations you must account for the lose of moles of HA + and the increase in moles of H and A .

KNOWING TO USE KA OR KB •





Depending on what species you have in solution you may need to use Ka or Kb to determine the pH of a solution. If the species you have produces H as a product you need to use Ka.

+

If the species you have produces OH as the product of the reaction you need to use Kb.

-

The following table provides pK and K values for selected weak acids. All values are from Martell, A. E.; a

a

Smith, R. M. Critical Stability Constants, Vols. 1–4. Plenum Press: New York, 1976. Unless otherwise stated, values are for 25 oC and zero ionic strength. Those values in brackets are considered less reliable.

SAMPLE PROBLEM

Weak acids are arranged alphabetically by the names of the neutral compounds from which they are derived. In some cases—such as acetic acid—the compound is the weak acid. In other cases—such as for the ammonium ion—the neutral compound is the conjugate base. Chemical formulas or structural formulas are shown for the fully protonated weak acid. Successive acid dissocation constants are provided for polyprotic weak acids; where there is ambiguity, the specific acidic proton is identified.

What is the pH of a solution prepared by dissolving 0.458 g of To find the K value for a conjugate weak base, recall that aminobenzene into K200 mL of water? ×K =K b

a

b

w

for a conjugate weak acid, HA, and its conjugate weak base, A–. Compound

Conjugate Acid

acetic acid

pKa

CH3COOH

Ka

4.757

1.75×10–5

4.42 5.42

3.8×10–5 3.8×10–6

2.348 (COOH) 9.867 (NH3)

4.49×10–3 1.36×10–10

4.601

2.51×10–5

3.232

5.86×10–4

2.08 (COOH) 4.96 (NH3)

8.3×10–3 1.1×10–5

O

adipic acid

HO

OH O

O

alanine

+

H3N

CH C

OH

CH3

aminobenzene 4-aminobenzene sulfonic acid

NH3+

NH3+

O3S COOH

2-aminobenozic acid NH3+

OH

–5

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