The catalytic activity of transitional metals is due to their variable oxidation states.
d and f Block Elements
Zinc is on the top position of hydrogen in electrochemical series.
So Zn displaces H 2 from dilute H 2 SO 4 and HCl with liberation of H 2 .
Zn + H 2 SO 4 ZnSO 4 + H 2 On the other hand HNO 3 is an oxidising agent.
Hydrogen obtained in this reaction is converted into H 2 O.
Zn + 2HNO 3 Zn(NO 3 ) 2 + 2H 2HNO 3 H 2 O + 2NO 2 + O 2H + O H 2 O.
Given electronic configuration of atom 1s 2 2s 2 2p 6 3s 2 3p 6 3d 3 4s 2 .
In the configuration, the last electron of the atom is filled in d sub-shell as 3d 3 .
Thus this element belongs to d-block of the periodic table with group no.
V.
Mn : [Ar] 3d 5 4s 2 Shows +2, +3, +4, +5, +6 & +7 oxidation states
General electronic configuration of lanthanides is
.
The most convenient method to protect the bottom of the ship made of iron is white tin plating preventing the build up of barnacles.
In lanthanides the basic character of hydroxides decreases as the ionic radius decreases.
La 3+ ions are larger than Li 3+ so it easily gives OH – ion thus La(OH) 3 is more basic than Li(OH) 3 .
Mn : [Ar] 3d 5 4s 2 Shows +2, +3, +4, +5, +6 & +7 oxidation states.
If the transition metal ion has unpaired electron then it shows colour.
Sc 3+ : [Ar] 18 3d 0 4s 0 Ti 3+ : [Ar] 18 3d 1 4s 0 Cr 4+ : [Ar] 18 3d 2 4s 0 V 3+ : [Ar] 18 3d 2 4s 0 Hence, Sc 3+ do not contain unpaired electron and hence it will not undergo d – d transition and do not show colour.
Option B: "A is correct but R is incorrect" is the right answer.
Here is the reasoning: Assertion A is correct.
In the complex
, if we assume the oxidation state of Ni to be x, we can set up the equation: From which we find that (x = 0).
Similarly, in
, if we let the oxidation state of Fe be y, the equation becomes: Solving this gives (y = 0).
Therefore, the oxidation states of both Ni and Fe are zero in their respective complexes, verifying that Assertion A is true.
Regarding Reason R, it is incorrect.
The low oxidation states in these complexes are stabilized through synergic bonding, which involves the ligand being a -acceptor, not a -donor.
The CO ligand in these complexes accepts electron density from the metal into its antibonding molecular orbitals, characterizing a -acid ligand, and not a -donor ligand as stated.
Consequently, Reason R does not hold true.