Final answer:
L-cysteine is a triprotic weak acid with three hydrolysis reactions, each associated with an equilibrium constant expression Kᵅ₁, Kᵅ₂, and Kᵅ₃, indicating the strength of each ionization step.
Step-by-step explanation:
The student asked to write all three hydrolysis reactions for the weak acid L-cysteine (H₃Cys) and its acid ionization expressions (Kᵅ₁, Kᵅ₂, and Kᵅ₃), including all ionic charges. L-cysteine is a triprotic acid meaning it can donate three protons (H⁺). The stepwise ionization processes result in the formation of different ionic species at each step, with corresponding equilibrium constants reflecting the strength of each ionization step.
The hydrolysis reactions for L-cysteine are as follows:
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- H₃Cys (aq) + H₂O (l) ⇌ H₂Cys⁻ (aq) + H₃O⁺ (aq) (First ionization)
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- H₂Cys⁻ (aq) + H₂O (l) ⇌ HCys²⁻ (aq) + H₃O⁺ (aq) (Second ionization)
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- HCys²⁻ (aq) + H₂O (l) ⇌ Cys³⁻ (aq) + H₃O⁺ (aq) (Third ionization)
The equilibrium constant expressions for these ionizations are as follows:
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- Kᵅ₁ = [H₂Cys⁻][H₃O⁺]/[H₃Cys]
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- Kᵅ₂ = [HCys²⁻][H₃O⁺]/[H₂Cys⁻]
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- Kᵅ₃ = [Cys³⁻][H₃O⁺]/[HCys²⁻]
Each expression describes the equilibrium state of each ionization step, where the square brackets represent the molar concentration of each species involved.