Acids and Bases

Acids and Bases

Definition: Acids are substances that donate hydrogen ions (H+) in solution, while bases accept them or donate hydroxide ions (OH-); the pH scale measures how acidic or basic a solution is on a range typically from 0 to 14.

How It Works

Three definitions layer on top of each other, each broader than the last:

  • Arrhenius: acid increases [H+] in water, base increases [OH-]. Only applies to aqueous solutions.
  • Brønsted-Lowry: acid is a proton (H+) donor, base is a proton acceptor. Explains why ammonia (NH3) is a base with no OH- to donate, it accepts a proton to form NH4+.
  • Lewis: acid accepts an electron pair, base donates one. Broadest definition, covers reactions with no protons at all, like BF3 reacting with NH3.

Conjugate pairs:

  • Every Brønsted-Lowry acid-base reaction produces a conjugate pair: when HA donates a proton, it becomes A-, its conjugate base.
  • The base that accepted the proton becomes its conjugate acid.
  • Strong acids dissociate essentially completely in water: HCl, HNO3, H2SO4, HBr, HI, HClO4.
  • Weak acids only partially dissociate, establishing an equilibrium: acetic acid, carbonic acid, HF.

Water autoionization:

  • Water is amphoteric, it can act as both acid and base.
2H2O ⇌ H3O+ + OH-
  • At 25°C, the autoionization equilibrium constant is Kw:
Kw = [H+][OH-] = 1.0 × 10⁻¹⁴
  • This is why pH + pOH = 14 in any aqueous solution at 25°C.

Polyprotic acids:

  • Some acids donate more than one proton, in sequential, increasingly difficult steps.
  • Sulfuric acid (H2SO4) loses its first proton almost completely, a strong acid in that step.
  • The resulting HSO4- is only moderately weak for the second proton.
  • Each successive Ka is smaller because pulling a proton from an increasingly negative species takes more energy.
  • Phosphoric acid (H3PO4) has three distinct Ka values:
Ka1 ≈ 7.5 × 10⁻³
Ka2 ≈ 6.2 × 10⁻⁸
Ka3 ≈ 4.2 × 10⁻¹³
  • Each is about five orders of magnitude smaller than the last.
  • This stepwise behavior is what makes phosphate useful as a biological buffer across a wide pH range.

Under the Hood

Core pH definitions:

pH = -log[H+]
pOH = -log[OH-]
pH + pOH = 14 (at 25°C)
  • Because the scale is logarithmic, each unit change means a tenfold change in H+ concentration.

Weak acid dissociation:

Ka = [H+][A-]/[HA]
pKa = -log(Ka)
Ka × Kb = Kw = 1.0 × 10⁻¹⁴
  • A lower pKa means a stronger acid.

Worked example 1: strong acid.

  • Given: 0.010 M HCl, dissociates completely
  • Step 1: [H+] = 0.010 M
pH = -log(0.010)
  • Answer: pH = 2.00

Worked example 2: weak acid.

  • Given: 0.100 M acetic acid, Ka = 1.8 × 10⁻⁵
  • Step 1: set up the equilibrium expression
CH3COOH ⇌ H+ + CH3COO-
Ka = x²/(0.100 - x) ≈ x²/0.100
  • Step 2: solve for x
x² = (1.8 × 10⁻⁵)(0.100) = 1.8 × 10⁻⁶
x = [H+] = 1.34 × 10⁻³ M
  • Step 3: convert to pH
pH = -log(1.34 × 10⁻³)
  • Answer: pH = 2.87
  • Note: only about 1.3% of the acetic acid molecules ionize, far less acidic than the strong acid at the same concentration.

Worked example 3: strong base.

  • Given: 0.0050 M NaOH
  • Step 1: [OH-] = 0.0050 M
pOH = -log(0.0050) = 2.30
pH = 14.00 - 2.30
  • Answer: pH = 11.70

Worked example 4: weak base.

  • Given: 0.050 M ammonia, Kb = 1.8 × 10⁻⁵
  • Step 1: set up the equilibrium expression
NH3 + H2O ⇌ NH4+ + OH-
Kb = x²/(0.050 - x) ≈ x²/0.050
  • Step 2: solve for x
x² = (1.8 × 10⁻⁵)(0.050) = 9.0 × 10⁻⁷
x = [OH-] = 9.49 × 10⁻⁴ M
  • Step 3: convert to pH
pOH = -log(9.49 × 10⁻⁴) = 3.02
pH = 14.00 - 3.02
  • Answer: pH = 10.98

Why It Matters

  • pH governs whether biological and industrial processes can proceed at all.
  • Enzymes have narrow pH ranges where they fold and function correctly.
  • Pepsin works around pH 2 in the stomach; trypsin needs the near-neutral small intestine.
  • Acid-base chemistry drives fertilizer production, water treatment, and food preservation.
  • It also drives the etching processes used in semiconductor manufacturing.
  • Ocean acidification, driven by CO2 dissolving into carbonic acid, is measurably shifting seawater pH.
  • This threatens calcium-carbonate-shelled marine organisms.

pH measurement in practice:

  • Indicators are weak acids or bases whose ionized and neutral forms have different colors.
  • Litmus turns red below about pH 4.5 and blue above about pH 8.3.
  • Phenolphthalein is colorless below pH 8.2 and pink above pH 10.
  • A pH meter measures the voltage across a glass membrane, generated by the [H+] difference between sample and internal reference.
  • That voltage converts to a pH reading via the Nernst equation, giving a continuous numeric value.

Common Pitfalls

  • Confusing “strong” with “concentrated”: a strong acid dissociates completely, a concentrated acid just has a lot of it dissolved. Dilute HCl is still a strong acid.
  • Forgetting pH is logarithmic: pH 3 is ten times more acidic than pH 4, not three-quarters as acidic.
  • Applying the “x is small” approximation in weak acid ICE tables when Ka is too large relative to concentration. Rough validity check: if Ka/C < 10⁻⁴, it’s safe to use.
  • Mixing up Ka and pKa, or forgetting the negative sign when converting between them.
  • Assuming neutralization always gives pH 7: a strong acid + weak base gives an acidic salt solution, a weak acid + strong base gives a basic one, because the conjugate species hydrolyzes water.
  • Treating polyprotic acids as if all protons dissociate equally; usually only the first step matters.
  • Reporting pH to more decimal places than the underlying [H+] measurement justifies; because pH is a logarithm, only digits after the decimal point count as significant figures.

Comparison

DefinitionAcidBaseScope
ArrheniusIncreases [H+] in waterIncreases [OH-] in waterAqueous only
Brønsted-LowryProton (H+) donorProton acceptorAny proton-transfer reaction
LewisElectron pair acceptorElectron pair donorBroadest, includes non-proton reactions
Conjugate acidForms when a base accepts H+—Brønsted-Lowry framework
Conjugate baseForms when an acid donates H+—Brønsted-Lowry framework
PropertyStrong AcidWeak Acid
Dissociation~100%Partial, governed by Ka
ExampleHCl, H2SO4CH3COOH, H2CO3
Conducts electricityStronglyWeakly
pH at given concentrationLower (more acidic)Higher
Equilibrium expression neededNoYes
Reaction with active metalsVigorous, fastSlower, less vigorous
Everyday SubstanceApproximate pHClassification
Battery acid0-1Strong acid
Stomach acid1.5-2Strong acid (dilute HCl)
Lemon juice2Weak acid
Coffee5Weak acid
Pure water7Neutral
Blood7.35-7.45Weakly basic (buffered)
Baking soda solution9Weak base
Ammonia cleaner11-12Weak base
Drain cleaner (NaOH)13-14Strong base

Example

Antacid tablets like Tums use calcium carbonate to neutralize excess stomach acid:

CaCO3(s) + 2HCl(aq) → CaCl2(aq) + H2O(l) + CO2(g)
  • The reaction consumes H+ ions directly, raising the stomach’s pH.
  • This relieves the burning sensation of acid reflux.
  • The fizzing some antacids produce is the CO2 gas escaping.

Real-World Application

Industrial wastewater treatment often requires neutralizing acidic effluent before it can legally be discharged.

  • Given: 10,000 L of wastewater at pH 2.00 (treated as a strong acid), neutralize to pH 7 using Ca(OH)2, molar mass 74.09 g/mol
  • Step 1: find [H+]
[H+] = 10⁻²·⁰⁰ = 0.0100 M
  • Step 2: find total moles of H+
mol H+ = 0.0100 mol/L × 10,000 L = 100 mol
  • Step 3: Ca(OH)2 supplies two OH- per formula unit
mol Ca(OH)2 needed = 100 mol H+ / 2 = 50 mol
  • Step 4: convert to mass
mass = 50 mol × 74.09 g/mol = 3,705 g
  • Answer: about 3.7 kg of Ca(OH)2 needed
  • Scaled to the millions of liters a real facility processes daily, this is why neutralizing agents are a significant ongoing line item in a treatment plant’s budget.

FAQ

Can a substance be both an acid and a base?

  • Yes, this is called being amphoteric, or amphiprotic for proton-transfer specifically.
  • Water is the classic example.
  • Bicarbonate (HCO3-) is another: it can donate a proton to become CO3²- or accept one to become H2CO3.

Does a higher concentration always mean a lower pH?

  • Only for a given acid.
  • Comparing across different acids, a dilute strong acid can have a lower pH than a concentrated weak acid.
  • Dissociation, not just concentration, controls [H+].

Why do pKa values matter for drug design?

  • A drug’s pKa determines what fraction is ionized at a given pH, via the Henderson-Hasselbalch equation.
  • Ionized versus neutral forms cross cell membranes at very different rates.
  • This directly affects absorption and how the drug distributes through the body.

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