25 Mn = [Ar] 3d 5 4s 2 Mn +3 = [Ar] 3d 4 CN – is a strong field ligand thus, it causes pairing of electrons in 3d-orbital.
As, coordination number of Mn = 6, so it will form an octahedral complex.
25 Mn = [Ar] 3d 5 4s 2 Mn +3 = [Ar] 3d 4 CN – is a strong field ligand thus, it causes pairing of electrons in 3d-orbital.
As, coordination number of Mn = 6, so it will form an octahedral complex.
The intensity of the trans-effect as measured by the increase in rate of substitution of the trans ligand) follows the sequence : CN > C 6 H 5 > Br > NH 3
Jahn-Teller distortion is generally significant for asymmetrically occupied e g orbitals as they are directed towards the ligands and the energy gain is more.
On the other hand in unevenly occupied t 2g orbitals, the John-Teller distortion is very weak.
Since the t 2g orbitals does not point directly at the ligand and thus energy gain is less.
[Fe(CO) 4 ] 2 has the lowest C—O bond order means the longest bond length.
Since metal atom is carrying maximum –ve charge therefore it would show maximum synergic bonding as a resultant C—O bond length would be maximum.
Total possible isomers = 3
[M (en) 2 (C 2 O 4 )]Cl x + 0 – 2 – 2 – 1 = 0 x = + 2 + 1 x = + 3 We know that coordination number is defined as the total number of binding sites attached to the metal.
Coordination number = 6 Sum of oxidation number and coordination number = 3 + 6 = 9
Electronic configuration of Ni 2+ : 3d 8 4s 0 Pairing of electrons in d-orbital takes place due to the presence of strong field ligand (CN - ).
[Fe(CN) 6 ] 3– x – 6 = –3 x = +6 – 3 x = +3 Hexa cyanido ferrate (III) ion.
[Co(CN) 6 ] 3 oxidation no. of Co = +3 Co +3 = [Ar] 3d 6 4s 0 CN – is a strong field ligand and as it approaches the metal ion the electrons must pair up.
[Co(CN) 6] 3– has no unpaired electrons and will be in a low spin configuration.
As For octahedral complexes, coordination number is 6.
CoCl 3 .
3NH 3 or [Co(NH 3 ) 3 Cl 3 ] will not give test for chloride ions with silver nitrate due to absence of ionisable chloride atoms.