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The Crystal Field Stabilization Energy (...

The Crystal Field Stabilization Energy (CFSE) of `[CoF_(3)(H_(2)O)_(3)](Delta_(0)lt P)` is :

A

`-0.8 Delta_(0)+2P`

B

`-0.8Delta_(0)`

C

`-0.4Delta_(0)`

D

`-0.4Delta_(0)+P`

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Knowledge Check

  • The crystal field stabilization energy (CFSE) in [Co(SCN)_(6)]^(3-) is :

    A
    `-2.4Delta_0`
    B
    `-1.8Delta_0`
    C
    `-4Delta_0`
    D
    `0Delta_0`

  • The crystal field stabilization energy (CFSE) is the highest for

    A
    `[CoF_4]^(2-)`
    B
    `Co(NCS)_4]^(2-)`
    C
    `[Co(NH_3)_6]^(3+)`
    D
    `[CoCl_4]^(2-)`

  • The crystal field stabilization energy (CFSE) is the highest for

    A
    `[CoF_(4)]^(2-)`
    B
    `[Co(NCS)_(4)]^(2-)`
    C
    `[Co(NH_(3))_(6)]^(3+)`
    D
    `[CoCl_(4)]^(2-)`

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    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 total crystal field stabilization energy (CFSE) for the complexes [Co(H_(2)O)_(6)]^(3+) and [CoF_(6)]^(3-) are respectively : (P is the pairing energy)

    The total crystal field stabilization energy (CFSE) for the complexes [Co(H_(2)O)_(6)]^(3+) and [CoF_(6)]^(3-) are respectively : (P is the pairing energy)

    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+) .

    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+) .

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