STATEMENT-1 The value of `Delta_(o)` for `M^(3+)` complexes are always much higher than value for `M^(2+)` complexes
STATEMENT-2 : The crystal field stabilization energy of `[Co(NH_(3))_(6)]^(3+) lt [Rh(NH_(3))_(6)]^(3+)`

The crystal field stabilisation energy of [Co(NH_(3))_(6)]Cl_(3) is:

The crystal field stabilisation energy of [Co(NH_(3))_(6)]Cl_(3) is:

Statement-1: The value of Delta_(0) for M^(3+) complexes are always much higher than value for M^(2+) complexes (for the same set of ligands) Statement-2: The crystal field stabilization energy of [Co(NH_(3))_(6)]^(3+)lt[Rh(NH_(3))_(6)]^(3+) .

Arrange the following complex ions in increasing order of crystal field splitting energy (Delta_(0):[Cr(Cl)_(6)]^(3-), [Cr(CN)_(6)]^(3-),[Cr(NH_(3))_(6)]^(3+)) .

Arrange the following complex ions in the increasing order of srystal field splitting energy (Delta_(0)),[Cr(CN)_(6)]^(3-),[Cr(CN)_(6)]^(3-),[Cr(NH_(3))_(6)]^(3+) .

Arrange following complex ions in increasing order of crystal field splitting energy (Delta_0) : [Cr(Cl_6]^(3-) , [Cr(CN)_6]^(3-) , [Cr(NH_3)_6]^(3+) .