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Question: The oxidation states of \({\text{Cr}}\) in \(\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} ...

The oxidation states of Cr{\text{Cr}} in [Cr(H2O)6]Cl3\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} \right)}_6}} \right]{\text{C}}{{\text{l}}_3} , [Cr(C6H6)2]\left[ {{\text{Cr}}{{\left( {{{\text{C}}_6}{{\text{H}}_6}} \right)}_2}} \right] , and K2[Cr(CN)2(O)2(O2)(NH3)]{{\text{K}}_2}\left[ {{\text{Cr}}{{\left( {{\text{CN}}} \right)}_2}{{\left( {\text{O}} \right)}_2}\left( {{{\text{O}}_2}} \right)\left( {{\text{N}}{{\text{H}}_3}} \right)} \right] respectively are:
A.+3 + 3 , 00 , and +6 + 6
B.+3 + 3 , 00 , and +4 + 4
C.+3 + 3 , +4 + 4 and +6 + 6
D.+3 + 3 , +2 + 2 and +4 + 4

Explanation

Solution

In this question, we have been asked to find out the oxidation states of a set of coordination complexes formed by the element chromium. The atomic number of chromium is 24 and the outermost electronic configuration of Cr{\text{Cr}} is [Ar]3d54s1\left[ {Ar} \right]3{d^5}4{s^1} .

Complete step by step solution:
The outermost electronic configuration of Cr{\text{Cr}} is [Ar]3d54s1\left[ {Ar} \right]3{d^5}4{s^1} .
We can calculate the oxidation state of Cr{\text{Cr}} in the following coordination complexes as follows:

[Cr(H2O)6]Cl3\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} \right)}_6}} \right]{\text{C}}{{\text{l}}_3}
Let us take the oxidation state of Cr{\text{Cr}} as xx.
We know that H2O{{\text{H}}_2}{\text{O}} is a neutral ligand. So, its charge is taken as zero.
As we observe the complex, we can understand that the complex is a cationic complex, since there are 3Cl3{\text{C}}{{\text{l}}^ - } ions outside the complex to neutralise the charge of the complex. The complex has an overall charge of +3 + 3 .
Therefore, in order to calculate the unknown value of xx , we can write an equation as,
x+(0×6)=+3x + (0 \times 6) = + 3
Therefore,
x=+3x = + 3
So, the oxidation state of Cr{\text{Cr}} in [Cr(H2O)6]Cl3\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} \right)}_6}} \right]{\text{C}}{{\text{l}}_3} is +3 + 3 .

[Cr(C6H6)2]\left[ {{\text{Cr}}{{\left( {{{\text{C}}_6}{{\text{H}}_6}} \right)}_2}} \right]
Let us take the oxidation state of Cr{\text{Cr}} as xx.
We know that benzene( C6H6{{\text{C}}_6}{{\text{H}}_6} ) is a neutral ligand. So, its charge is taken to be zero. The complex is a neutral complex. This means that the overall charge of the complex is zero.
Therefore, in order to calculate the unknown value of xx , we can write an equation as,
x+(0×2)=0x + (0 \times 2) = 0
Therefore,
x=0x = 0
So, the oxidation state of Cr{\text{Cr}} in [Cr(C6H6)2]\left[ {{\text{Cr}}{{\left( {{{\text{C}}_6}{{\text{H}}_6}} \right)}_2}} \right] is 00 .

K2[Cr(CN)2(O)2(O2)(NH3)]{{\text{K}}_2}\left[ {{\text{Cr}}{{\left( {{\text{CN}}} \right)}_2}{{\left( {\text{O}} \right)}_2}\left( {{{\text{O}}_2}} \right)\left( {{\text{N}}{{\text{H}}_3}} \right)} \right]
Let us take the oxidation state of Cr{\text{Cr}} as xx.
The ligands in the complex are CN{\text{C}}{{\text{N}}^ - } , O2{{\text{O}}^{2 - }} , O2{\text{O}}_2^ - , which are anionic ligands and NH3{\text{N}}{{\text{H}}_3} , which is a neutral ligand.
The given complex is an anionic complex having a charge of 2 - 2 which is neutralised by 2K+2{{\text{K}}^ + } ions outside the coordination complex. This means that the charge of the complex is 2 - 2 .
Therefore, in order to calculate the unknown value of xx , we can write an equation as,
x+(1×2)+(2×2)+(1×2)+0=2x + ( - 1 \times 2) + ( - 2 \times 2) + ( - 1 \times 2) + 0 = - 2
Solving the equation, we get,
x+(2)+(4)+(2)+0=2x + ( - 2) + ( - 4) + ( - 2) + 0 = - 2
The equation can be further simplified as,
x8=2x - 8 = - 2
We get,
x=2+8x = - 2 + 8
Therefore,
x=+6x = + 6
So, the oxidation state of Cr{\text{Cr}} in K2[Cr(CN)2(O)2(O2)(NH3)]{{\text{K}}_2}\left[ {{\text{Cr}}{{\left( {{\text{CN}}} \right)}_2}{{\left( {\text{O}} \right)}_2}\left( {{{\text{O}}_2}} \right)\left( {{\text{N}}{{\text{H}}_3}} \right)} \right] is +6 + 6 .

Hence, option (A) is the correct answer.

Note:
Knowing the outermost electronic configuration of 3d3d transition elements and the various types of ligands – cationic, anionic and neutral, involved in the formation of coordination complexes would be helpful in calculating the oxidation state of central transition metal ion in the complex.