
The oxidation states of ${\text{Cr}}$ in $\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} \right)}_6}} \right]{\text{C}}{{\text{l}}_3}$ , $\left[ {{\text{Cr}}{{\left( {{{\text{C}}_6}{{\text{H}}_6}} \right)}_2}} \right]$ , and ${{\text{K}}_2}\left[ {{\text{Cr}}{{\left( {{\text{CN}}} \right)}_2}{{\left( {\text{O}} \right)}_2}\left( {{{\text{O}}_2}} \right)\left( {{\text{N}}{{\text{H}}_3}} \right)} \right]$ respectively are:
A.$ + 3$ , $0$ , and $ + 6$
B.$ + 3$ , $0$ , and $ + 4$
C.$ + 3$ , $ + 4$ and $ + 6$
D.$ + 3$ , $ + 2$ and $ + 4$
Answer
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Hint: 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 ${\text{Cr}}$ is $\left[ {Ar} \right]3{d^5}4{s^1}$ .
Complete step by step answer:
The outermost electronic configuration of ${\text{Cr}}$is $\left[ {Ar} \right]3{d^5}4{s^1}$ .
We can calculate the oxidation state of ${\text{Cr}}$ in the following coordination complexes as follows:
$\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} \right)}_6}} \right]{\text{C}}{{\text{l}}_3}$
Let us take the oxidation state of ${\text{Cr}}$ as $x$.
We know that ${{\text{H}}_2}{\text{O}}$ 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 $3{\text{C}}{{\text{l}}^ - }$ ions outside the complex to neutralise the charge of the complex. The complex has an overall charge of $ + 3$ .
Therefore, in order to calculate the unknown value of $x$ , we can write an equation as,
$x + (0 \times 6) = + 3$
Therefore,
$x = + 3$
So, the oxidation state of ${\text{Cr}}$ in $\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} \right)}_6}} \right]{\text{C}}{{\text{l}}_3}$ is $ + 3$ .
$\left[ {{\text{Cr}}{{\left( {{{\text{C}}_6}{{\text{H}}_6}} \right)}_2}} \right]$
Let us take the oxidation state of ${\text{Cr}}$ as $x$.
We know that benzene( ${{\text{C}}_6}{{\text{H}}_6}$ ) 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 $x$ , we can write an equation as,
$x + (0 \times 2) = 0$
Therefore,
$x = 0$
So, the oxidation state of ${\text{Cr}}$ in $\left[ {{\text{Cr}}{{\left( {{{\text{C}}_6}{{\text{H}}_6}} \right)}_2}} \right]$ is $0$ .
${{\text{K}}_2}\left[ {{\text{Cr}}{{\left( {{\text{CN}}} \right)}_2}{{\left( {\text{O}} \right)}_2}\left( {{{\text{O}}_2}} \right)\left( {{\text{N}}{{\text{H}}_3}} \right)} \right]$
Let us take the oxidation state of ${\text{Cr}}$ as $x$.
The ligands in the complex are ${\text{C}}{{\text{N}}^ - }$ , ${{\text{O}}^{2 - }}$ , ${\text{O}}_2^ - $ , which are anionic ligands and ${\text{N}}{{\text{H}}_3}$ , which is a neutral ligand.
The given complex is an anionic complex having a charge of $ - 2$ which is neutralised by $2{{\text{K}}^ + }$ ions outside the coordination complex. This means that the charge of the complex is $ - 2$ .
Therefore, in order to calculate the unknown value of $x$ , we can write an equation as,
$x + ( - 1 \times 2) + ( - 2 \times 2) + ( - 1 \times 2) + 0 = - 2$
Solving the equation, we get,
$x + ( - 2) + ( - 4) + ( - 2) + 0 = - 2$
The equation can be further simplified as,
$x - 8 = - 2$
We get,
$x = - 2 + 8$
Therefore,
$x = + 6$
So, the oxidation state of ${\text{Cr}}$ in ${{\text{K}}_2}\left[ {{\text{Cr}}{{\left( {{\text{CN}}} \right)}_2}{{\left( {\text{O}} \right)}_2}\left( {{{\text{O}}_2}} \right)\left( {{\text{N}}{{\text{H}}_3}} \right)} \right]$ is $ + 6$ .
Hence, option (A) is the correct answer.
Note:
Knowing the outermost electronic configuration of $3d$ 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 ions in the complex.
Complete step by step answer:
The outermost electronic configuration of ${\text{Cr}}$is $\left[ {Ar} \right]3{d^5}4{s^1}$ .
We can calculate the oxidation state of ${\text{Cr}}$ in the following coordination complexes as follows:
$\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} \right)}_6}} \right]{\text{C}}{{\text{l}}_3}$
Let us take the oxidation state of ${\text{Cr}}$ as $x$.
We know that ${{\text{H}}_2}{\text{O}}$ 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 $3{\text{C}}{{\text{l}}^ - }$ ions outside the complex to neutralise the charge of the complex. The complex has an overall charge of $ + 3$ .
Therefore, in order to calculate the unknown value of $x$ , we can write an equation as,
$x + (0 \times 6) = + 3$
Therefore,
$x = + 3$
So, the oxidation state of ${\text{Cr}}$ in $\left[ {{\text{Cr}}{{\left( {{{\text{H}}_2}{\text{O}}} \right)}_6}} \right]{\text{C}}{{\text{l}}_3}$ is $ + 3$ .
$\left[ {{\text{Cr}}{{\left( {{{\text{C}}_6}{{\text{H}}_6}} \right)}_2}} \right]$
Let us take the oxidation state of ${\text{Cr}}$ as $x$.
We know that benzene( ${{\text{C}}_6}{{\text{H}}_6}$ ) 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 $x$ , we can write an equation as,
$x + (0 \times 2) = 0$
Therefore,
$x = 0$
So, the oxidation state of ${\text{Cr}}$ in $\left[ {{\text{Cr}}{{\left( {{{\text{C}}_6}{{\text{H}}_6}} \right)}_2}} \right]$ is $0$ .
${{\text{K}}_2}\left[ {{\text{Cr}}{{\left( {{\text{CN}}} \right)}_2}{{\left( {\text{O}} \right)}_2}\left( {{{\text{O}}_2}} \right)\left( {{\text{N}}{{\text{H}}_3}} \right)} \right]$
Let us take the oxidation state of ${\text{Cr}}$ as $x$.
The ligands in the complex are ${\text{C}}{{\text{N}}^ - }$ , ${{\text{O}}^{2 - }}$ , ${\text{O}}_2^ - $ , which are anionic ligands and ${\text{N}}{{\text{H}}_3}$ , which is a neutral ligand.
The given complex is an anionic complex having a charge of $ - 2$ which is neutralised by $2{{\text{K}}^ + }$ ions outside the coordination complex. This means that the charge of the complex is $ - 2$ .
Therefore, in order to calculate the unknown value of $x$ , we can write an equation as,
$x + ( - 1 \times 2) + ( - 2 \times 2) + ( - 1 \times 2) + 0 = - 2$
Solving the equation, we get,
$x + ( - 2) + ( - 4) + ( - 2) + 0 = - 2$
The equation can be further simplified as,
$x - 8 = - 2$
We get,
$x = - 2 + 8$
Therefore,
$x = + 6$
So, the oxidation state of ${\text{Cr}}$ in ${{\text{K}}_2}\left[ {{\text{Cr}}{{\left( {{\text{CN}}} \right)}_2}{{\left( {\text{O}} \right)}_2}\left( {{{\text{O}}_2}} \right)\left( {{\text{N}}{{\text{H}}_3}} \right)} \right]$ is $ + 6$ .
Hence, option (A) is the correct answer.
Note:
Knowing the outermost electronic configuration of $3d$ 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 ions in the complex.
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