Free Online Flashcard Deck

13/14 Acid–Base and Solubility Equilibria Free Online FlashCards

Study 13/14 Acid–Base and Solubility Equilibria with 12 free online flashcards. Review key terms, definitions, and concepts with this interactive flashcard deck.

12 cards
01
Front

What do Arrhenius acids and bases produce in water?

Back

An Arrhenius acid produces H₃O⁺ in water, while an Arrhenius base produces OH⁻ in water.

02
Front

What defines a Brønsted–Lowry acid–base pair?

Back

A Brønsted–Lowry acid donates a proton, and a Brønsted–Lowry base accepts a proton. A conjugate acid–base pair differs by one proton.

03
Front

What distinguishes Lewis acids from Lewis bases?

Back

A Lewis acid accepts an electron pair, whereas a Lewis base donates an electron pair. In BF₃ + NH₃, BF₃ is the acid and NH₃ is the base.

04
Front

What relationship connects pH and pOH at 25 °C?

Back

At 25 °C, pH + pOH = 14.00 because Kᵥ = [H₃O⁺][OH⁻] = 1.0 × 10⁻¹⁴.

05
Front

Why is [OH⁻] ≈ 2C for Ba(OH)₂?

Back

For Ba(OH)₂, [OH⁻] ≈ 2CBa(OH)₂ because each formula unit supplies two hydroxide ions.

06
Front

How do Kₐ and pKₐ indicate acid strength?

Back

A larger Kₐ means a stronger acid, while a lower pKₐ means a stronger acid because pKₐ = −log Kₐ.

07
Front

When is the weak-acid approximation [H₃O⁺] ≈ √(KₐC) valid?

Back

For a weak acid of concentration C, [H₃O⁺] ≈ √(KₐC) when ionization is less than about 5% of C.

08
Front

Why is a sodium acetate solution basic?

Back

Acetate hydrolysis produces OH⁻, so sodium acetate solutions are basic: CH₃CO₂⁻ + H₂O ⇌ CH₃CO₂H + OH⁻.

09
Front

What equation gives the pH of an acidic buffer?

Back

The Henderson–Hasselbalch equation is pH = pKₐ + log([A⁻]/[HA]). Mole ratios may replace concentration ratios when both species share the solution.

10
Front

When is an acidic buffer most effective?

Back

A buffer is most effective when [A⁻] = [HA], because then pH = pKₐ. To design a buffer, choose a weak acid with pKₐ near the target pH.

11
Front

How do equivalence point and endpoint differ?

Back

The equivalence point is reached when stoichiometrically equivalent amounts have reacted. The endpoint is the observed indicator or instrumental signal and should closely match equivalence.

12
Front

What is true at the half-equivalence point?

Back

At the half-equivalence point of a weak-acid–strong-base titration, [HA] = [A⁻], so the Henderson–Hasselbalch equation gives pH = pKₐ.