Configuration
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Configuration
Advanced
Proton Count
Common Polyprotic Acids
Buffer Type
Buffer Capacity (optional)
Salt Type
pH 7.000
Neutral Strong
Step-by-Step Solution
JEE Formula Reference
Strong Acid
pH = –log(n·C)
Strong Base
pOH = –log(n·C) → pH = 14 – pOH
Weak Acid (approx)
[H⁺] = √(Ka·C); α = √(Ka/C)
Weak Base (approx)
[OH⁻] = √(Kb·C)
Henderson–Hasselbalch
pH = pKa + log([A⁻]/[HA])
Salt of Weak Acid
pH = 7 + ½(pKa + log C)
Salt of Weak Base
pH = 7 – ½(pKb + log C)
Weak Acid + Weak Base
pH = 7 + ½(pKa – pKb)
Degree of Hydrolysis
h = √(Kw / Ka·C)
Kw at 25°C
Kw = 1.0 × 10⁻¹⁴

Expert FAQ: pH & Acid-Base Equilibrium

Can pH be negative?

Yes. If $[H^+] > 1\text{ M}$ (e.g., concentrated $HCl$), pH becomes negative. At 10 M HCl, pH ≈ –1.

What is the n-Factor for H₂SO₄?

H₂SO₄ is diprotic so n = 2. A 0.5 M H₂SO₄ solution delivers $[H^+] = 1.0\text{ M}$, giving pH = 0.

When is the quadratic method necessary?

When $C/Ka < 100$, i.e., concentration is low relative to Ka. In this case the approximation $x \ll C$ fails and the full ICE quadratic $x^2 + Kax – KaC = 0$ must be solved.

How does temperature affect pH?

As temperature rises, $K_w$ increases, so the neutral point drops below 7. At 37°C (body temp), neutral pH ≈ 6.82.

Henderson–Hasselbalch limitations?

Applies only when $[HA]/[A^-]$ ratio is between 0.1 and 10 (i.e., pH within ±1 of pKa). At extremes the approximation breaks down.

What is $K_w$ and how does it change?

$K_w = [H^+][OH^-] = 10^{-14}$ at 25°C. Endothermic reaction — rising temperature increases $K_w$.