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Although acetylsalicylic acid (aspirin) is a well-known and widely used analgesic and anti-inflammatory agent, copper(II) acetylsalicylate, a copper complex formed from aspirin and copper, has also been found to exhibit some distinctive and potentially beneficial pharmacological properties. Formation of copper(II) acetylsalicylate is achieved when the conjugate base of aspirin, acetylsalicylate (C9H7O4−) , binds to Cu2+ ions in solution, as outlined in Reaction 1.4 NaC9H7O4(aq) + 2 CuSO4(aq) → Cu2(C9H7O4) 4(s) + 2 Na2SO4(aq) Reaction 1Using Reaction 1, a researcher synthesized a sample of copper(II) acetylsalicylate for analysis. A small volume of 0.50 M aqueous copper(II) sulfate (molar mass = 159.6) was mixed into 100 mL of filtered, saturated aqueous sodium acetylsalicylate (molar mass = 202.2) at room temperature and slowly stirred. Formation of copper(II) acetylsalicylate (molar mass = 843.7) was immediately observed as a bright blue precipitate. The precipitate was then isolated by filtration and dried, affording the product complex in high yield.
Adapted from: Seguel GV, Rivas BL, Contreras JG. Synthesis and characterization of copper complexes: interaction of metalliccarboxylates with 1,3-thiazole ligand. Journal of the Chilean Chemical Society. 1970; 58(4) :1967.
-The copper(II) acetylsalicylate product immediately precipitates from the reaction solution because:
A) [Cu2+]2 multiplied by [C9H7O4−]4 is less than the Ksp of Cu2(C9H7O4) 4.
B) the sum of [Cu2+]2 and [C9H7O4−]4 is less than the Ksp of Cu2(C9H7O4) 4.
C) [Cu2+]2 multiplied by [C9H7O4−]4 is greater than the Ksp of Cu2(C9H7O4) 4.
D) the sum of [Cu2+]2 and [C9H7O4−]4 is greater than the Ksp of Cu2(C9H7O4) 4.
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