The hybridisation of [FeF₆]^3- is:

The compound with the highest magnetic moment value is:

1. \( {\left[\mathrm{Cr}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{3+}} \)
2. \( {\left[\mathrm{Fe}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+}} \)
3. \({\left[\mathrm{Zn}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+}} \)
4. \( {\left[\mathrm{Ti}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+}}\)

The difference between a weak field ligand and a strong field ligand is:

The crystal field splitting energy is:

[Cr(NH₃)₆]³⁺ is paramagnetic ,while ${\left[\mathrm{Ni}{\left(\mathrm{CN}\right)}_4\right]}^{2-}$ is diamagnetic because:

The greater value of the stability constant of complex salt indicates:

1. The greater proportion of products.

2. The greater proportion of reactants

3. Lesser concentration of catalyst at equilibrium

4. All of the above

The correct order for the wavelengths of absorption in the visible region for the following is:
\(\left[\mathrm{Ni}\left(\mathrm{NO}_2\right)_6\right]^{4-},\left[\mathrm{Ni}\left(\mathrm{NH}_3\right)_6\right]^{2+},\left[\mathrm{Ni}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{2+}\)
1. $[\mathrm{Ni}{\left({\mathrm{H}}_2\mathrm{O}\right)}_6{]}^{2+}$ < $[\mathrm{Ni}{\left({\mathrm{NH}}_3\right)}_6{]}^{2+}$ < $[\mathrm{Ni}{\left({\mathrm{NO}}_2\right)}_6{]}^{4-}$

2. $[\mathrm{Ni}{\left({\mathrm{H}}_2\mathrm{O}\right)}_6{]}^{2+}$ > $[\mathrm{Ni}{\left({\mathrm{NH}}_3\right)}_6{]}^{2+}$ > $[\mathrm{Ni}{\left({\mathrm{NO}}_2\right)}_6{]}^{4-}$

3. $[\mathrm{Ni}{\left({\mathrm{NH}}_3\right)}_6{]}^{2+}$ > $[\mathrm{Ni}{\left({\mathrm{H}}_2\mathrm{O}\right)}_6{]}^{2+}$> $[\mathrm{Ni}{\left({\mathrm{NO}}_2\right)}_6{]}^{4-}$

4.  $[\mathrm{Ni}{\left({\mathrm{H}}_2\mathrm{O}\right)}_6{]}^{2+}$ > ${\left[\mathrm{Ni}{\left({\mathrm{NO}}_2\right)}_6\right]}^{4-}$> [Ni(NH₃)₆]²⁺

The number of unpaired electrons in the following complexes respectively are-

${\mathrm{K}}_4\left[\mathrm{Mn}{\left(\mathrm{CN}\right)}_6\right],<mspace\; width="1em"></mspace>\mathrm{Fe}{\left({\mathrm{H}}_2\mathrm{O}\right)}_6{]}^{2+},<mspace\; width="1em"></mspace>{\mathrm{K}}_2\left[{\mathrm{MnCl}}_4\right]$

1. 1, 4, 5

2. 2, 4, 5

3. 0, 3, 4

4. 2, 3, 4

The correct splitting diagram of d orbitals in an octahedral crystal field is:

1.		2.
3.		4.	None of the above