Is Hydrazine (N₂H₄) a Strong or Weak Base?

Is Hydrazine (N₂H₄) a strong or weak base?

Hydrazine (H2N-NH2) is a weak diprotic base - both nitrogen atoms have lone pairs that can accept protons. It is weaker than ammonia because the adjacent nitrogen is electron-withdrawing.

FormulaN₂H₄
NameHydrazine
CategoryWeak base
pKa8.1
ConjugateHydrazinium ion (N₂H₅⁺)
Key ConceptDiprotic base

Definition

Hydrazine has two -NH2 groups connected by an N-N bond. Each nitrogen can accept a proton, making it a diprotic base.

Acidic Proton / Active Site

Hydrazine acts as a base, not an acid. Both nitrogen lone pairs can accept protons, though the first protonation is much easier than the second.

Conjugate Pair

N2H4 + H+ -> N2H5+ (first protonation). N2H5+ + H+ -> N2H6^2+ (second, much weaker). The adjacent NH3+ group makes the second protonation very difficult.

Strength Classification

Kb1 = 1.3 x 10^-6, weaker than ammonia. The second nitrogen is electron-withdrawing, reducing electron density on each N compared to ammonia.

See acidic protons, conjugate base overlays, and pKa labels on interactive 3D molecules.

Explore Hydrazine's Acid-Base Properties in 3D

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