- A$[Cu(NH_3)_4]^{2+} < [Cu(en)_2]^{2+} < [Cu(trien)]^{2+}$
- ✓$[Fe(H_2O)_6]^{3+} < [Fe(NO_2)_6]^{3-} < [Fe(NH_3)_6]^{3+}$
- C$[Co(H_2O)_6]^{3+} < [Rh(H_2O)_6]^{3+} < [Ir(H_2O)_6]^{3+}$
- D$[Cr(NH_3)_6]^{1+} < [Cr(NH_3)_6]^{2+} < [Cr(NH_3)_6]^{3+}$
$(a)\, [Cu(NH_3)_4]^{2+} < [Cu(en)_2]^{2+} < [Cu(trien)]^{2+}$
Their formation entropy increases in the same order, because denticity of ligand increases
$(b)\, [Fe(H_2O)_6]^{3+} < [Fe(NO_2)_6]^{3-} < [Fe(NH_3)_6]^{3+}$
$NO_2^-$ is stronger ligand than $NH_3$
$(c)\, [Co(H_2O)_6]^{3+} < [Rh(H_2O)_6]^{3+} < [Ir(H_2O)_6]^{3+}$
$Z_{eff}$ value increases from $Co^{3+}$ to $Ir^{3+}$
$(d)\, [Cr(NH_3)_6]^{1+} < [Cr(NH_3)_6]^{2+} < [Cr(NH_3)_6]^{3+}$
Oxidation state of $Cr$ atom increases from $+ 1$ to $+3$.
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$\mathop {(A)}\limits_{ gives\,\,positive ~\\ iodoform\,Test } \xrightarrow[\begin{subarray}{l} (ii)\,{H^ + },{H_2}O + ~\\ (iii)\,conc.\,{H_2}S{O_4}/\Delta \end{subarray} ]{{{\text{(i) C}}{{\text{H}}_{\text{3}}}{\text{MgBr}}}}(B)\xrightarrow{{{O_3}/Zn,{H_2}O}}$
$\xrightarrow[\Delta ]{{{H^ \oplus }}}\,B$
The product $"B"$ is