- A$- 1.8 \Delta _o$
- B$- 1.6 \Delta _o + P$
- C$- 1.2 \Delta _o$
- ✓$- 0.6 \Delta _o$
electrons of lower energy d-orbitals would be higher than that required to place the electrons in the higher d-orbital.
Thus, pairing does not occur.
For high spin $d^{4}$ octahedral complex Crystal fleld stabilisation energy
$=(-3 \times 0.4+1 \times 0.6) \Delta_{0}$
$=(-1.2+0.6) \Delta_{0}=-0.6 \Delta_{0}$
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$A_{(g)} \longrightarrow B_{(g)} + C_{(g)}$
The initial pressure of the system before deomposition of $A$ was $P_i$. After time $'t'$ total pressure of the system increased by $x\, units$ and become $'P_t'$. The rate constant $k$ for reaction is given as
| List$-I$ | List$-II$ | ||
| $(P)$ | $[Cr(NH_3)_4Cl_2]Cl$ | $(1)$ | Paramagnetic and exhibits ionisation isomerism |
| $(Q)$ | $[Ti(H_2O)_5Cl](NO_3)_2$ | $(2)$ | Diamagnetic and exhibits cis-trans isomerism |
| $(R)$ | $[Pt(en)(NH_3)Cl]NO_3$ | $(3)$ | Paramagnetic and exhibits cis-trans isomerism |
| $(S)$ | $[Co(NH_3)_4(NO_3)_2]NO_3$ | $(4)$ | Diamagnetic and exhibits ionisation isomerism |
$(I)$ cis $- [Co(NH_3)_2(en)_2]^{3+}$ $(II)$ trans $-[IrCl_2(C_2O_4)_2]^{3-}$
$(III)\, [Rh(en)_3]^{3+}$ $(IV)$ cis $-[Ir(H_2O)_3Cl_3$
