Match List - I with List - II:
List - I:
(A) \([ \text{MnBr}_4]^{2-}\)
(B) \([ \text{FeF}_6]^{3-}\)
(C) \([ \text{Co(C}_2\text{O}_4)_3]^{3-}\)
(D) \([ \text{Ni(CO)}_4]\)
List - II:
(I) d²sp³ diamagnetic
(II) sp²d² paramagnetic
(III) sp³ diamagnetic
(IV) sp³ paramagnetic
To solve the problem of matching List-I with List-II, we need to determine the hybridization of each complex and their magnetic properties:
Thus, the correct matches are:
List-I | List-II |
---|---|
(A) \([ \text{MnBr}_4]^{2-}\) | (III) sp³ diamagnetic |
(B) \([ \text{FeF}_6]^{3-}\) | (II) sp²d² paramagnetic |
(C) \([ \text{Co(C}_2\text{O}_4)_3]^{3-}\) | (I) d²sp³ diamagnetic |
(D) \([ \text{Ni(CO)}_4]\) | (IV) sp³ paramagnetic |
The correct answer is:
(A)-(III),(B)-(II),(C)-(I),(D)-(IV)
Werner’s coordination theory in 1893 was the first attempt to explain the bonding in coordination complexes. It must be remembered that this theory was put forward before the electron had been discovered by J.J. Thomson in 1897, and before the electronic theory of valency. Werner did not have any of the modern instrumental techniques and all his studies were made using simple experimental techniques. Werner was able to explain the nature of bonding in complexes and he concluded that in complexes, the metal shows two different sorts of valency: primary and secondary. Primary valences are normally ionisable whereas secondary valences are non-ionisable.
The largest $ n \in \mathbb{N} $ such that $ 3^n $ divides 50! is:
The term independent of $ x $ in the expansion of $$ \left( \frac{x + 1}{x^{3/2} + 1 - \sqrt{x}} \cdot \frac{x + 1}{x - \sqrt{x}} \right)^{10} $$ for $ x>1 $ is: