3.2.6 Reactions Of Ions In Aqueous Solution Flashcards
Name 4 metal-aqua ions + their colour
[Fe(H2O)6]^2+ - green solution
[Cu(H2O)6]^2+ - blue solution
[Fe(H2O)6]^3+ - purple solution
[Al(H2O)6]^3+ - colourless solution
Reaction of [Fe(H2O)6]^2+ (aq) with NaOH
Deprotonation
Drops- green ppt formed- goes brown on standing in air Fe(H2O)4(OH)2(s)
Excess- no further change
Reaction of [Cu(H2O)6]^2+ (aq) with NaOH
Deprotonation
Drops- blue ppt formed Cu(H2O)4(OH)2(s)
Excess- no further change
Reaction of [Fe(H2O)6]^3+ (aq) with NaOH
Deprotonation
Drops- brown ppt formed Fe(H2O)3(OH)3(s)
Excess- no further change
Reaction of [Al(H2O)6]^3+ (aq) with NaOH
Deprotonation
Drops- white ppt formed Al(H2O)3(OH)3(s)
Excess- no further change
Reaction of [Fe(H2O)6]^2+ (aq) with NH3
Deprotonation
Drops- green ppt formed- goes brown on standing in air Fe(H2O)4(OH)2(s)
Excess- no further change
Reaction of [Cu(H2O)6]^2+ (aq) with NH3
Deprotonation
Drops- blue ppt formed Cu(H2O)4(OH)2(s)
Excess- deep blue solution formed [Cu(H2O)2(NH3)4]2(aq)
Reaction of [Fe(H2O)6]^3+ (aq) with NH3
Deprotonation
Drops- brown ppt formed Fe(H2O)3(OH)3(s)
Excess- no further change
Reaction of [Al(H2O)6]^3+ (aq) with NH3
Deprotonation
Drops- white ppt formed Al(H2O)3(OH)3(s)
Excess- no further change
Reaction of [Fe(H2O)6]^2+ (aq) with Na2CO3
Green ppt FeCO3(s)
Reaction of [Cu(H2O)6]^2+ (aq) with Na2CO3
Blue-green ppt CuCO3(s)
Reaction of [Fe(H2O)6]^3+ (aq) with Na2CO3
Brown ppt Fe(H2O)3(OH)3(s) + CO2(g)
Reaction of [Al(H2O)6]^3+ (aq) with Na2CO3
White ppt Al(H2O)3(OH)3(s) + CO2 (g)
Explain, with the use of an equation, why a solution containing [Al(H2O)6]3+ has
a pH ˂7
[Al(H2O)6]^3+ <=> [Al((H2O)5OH]^2+ + H^+
Describe metal aqua complexes
Water molecules form coordinate bonds with central metal ions
What determines the acidity of metal aqua ions in aqueous solution
The charge of central ion
Higher charge density = more acidic
Pull of electrons in O-H bonds away from H towards ion stronger, releasing the H^+ ion
Why are complexes formed with multidentate ligands more stable than those with monodentate ligands
Ligands attached at multiple points to metal ion more strongly attracted
Chelate effect