Coordination Compounds
Which of the following has no net dipole moment?
Which of the following complex ion is expected to absorb light in the visible region?
Only those transition metal complexes are expected to absorb visible light, in which d- subshell is incomplete and excitation of an electron from a lower energy orbital to higher energy orbital is possible.
(a) In $$\left[ Sc({ H }_{ 2 }O)({ NH }_{ 3 })_{ 3 } \right] ^{ 3+ }$$ Sc is present in $$ { Sc }^{ 3+ }$$=$$[Ar]3{ d }^{ 0 },4{ s }^{ 0 }$$
Since in this complex excitation of the electron is not possible, it will not absorb visible light.
(b) $$\left[ Ti(en)_{ 2 }(N{ H }_{ 3 })_{ 2 } \right] ^{ 4+ },$$ Ti is present as $${ Ti }^{ 4+ }$$
$${ Ti }^{ 4+ }=[Ar]3{ d }^{ 0 },4{ s }^{ 0 }$$
Hence it will not absorb visible light
(c) In $$\left[ Cr({ NH }_{ 3 })_{ 6 } \right] ^{ 3+ }$$ Cr is present as $${ Cr }^{ 3+ }$$
$${ Cr }^{ 3+ }$$=$$[Ar]3{ d }^{ 3 },4{ s }^{ 0 }$$
Since this complex has three unpaired electrons excitation of electrons is possible and thus, it is expected that this complex will absorb visible light.
(d) In $$\left[ Zn(N{ H }_{ 3 })_{ 6 } \right] ^{ 2+ }$$ Zn is present as $${ Zn }^{ 2+ }$$
$${ Zn }^{ 2+ }$$=$$[Ar]3{ d }^{ 10 },4{ s }^{ 0 }$$
Hence , this complex will not absorb visible light.
The correct option is C.
Which of the following has no net dipole moment?
Which of the following metal ion is present in Ziegler-Natta catalyst?
Which plays a major role in the formation of complex compound?
TEL is a compound used as
Copper sulphate dissolves in ammonia due to the formation of:
The correct increasing order of trans-effect of the following species is:
In calcium fluoride, having the fluorite structure, the coordination numbers for calcium ion $$(Ca^{2+})$$ and fluoride ion $$(F^-)$$ are:
Specify the oxidation numbers of the metals in the following coordination entities: (i) $$[Co(H_{2}O)(CN)(en)_{2}]^{2+}$$ (ii) $$[CoBr_{2} (en)_{2}]^{+}$$ (iii) $$[PtCl_{4}]^{2-}$$ (iv) $$K_{3} [Fe(CN)_{6}]$$ (v) $$[Cr(NH_{3})_{3}Cl_{3}]$$
Aqueous copper sulphate solution (blue in colour) gives: (i) a green precipitate with aqueous potassium fluoride and (ii) a bright green solution with aqueous potassium chloride. Explain these experimental results.
What is the coordination entity formed when excess of aqueous KCN is added to an aqueous solution of copper sulphate? Why is it that no precipitate of copper sulphide is obtained when H2S(g) is passed through this solution?