Wilkinsion catalyst is [(Ph3P)3RhCl]
d and f Block Elements
To identify the incorrect statement, let's analyze each option : Option A : "In manganate and permanganate ions, the π-bonding takes place by overlap of p-orbitals of oxygen and d-orbitals of manganese." This statement is true.
In both manganate and permanganate ions, the manganese atom is in a high oxidation state (+6 and +7, respectively) and forms bonds with oxygen atoms involving the overlap of p-orbitals of oxygen and d-orbitals of manganese.
Option B : "Manganate ion is green in colour and permanganate ion in purple in colour." This statement is true.
Manganate ions are indeed green and permanganate ions are purple in aqueous solution.
Option C : "Manganate and permanganate ions are paramagnetic." This statement is incorrect.
Both manganate and permanganate ions are diamagnetic, not paramagnetic.
In these ions, manganese is in +6 and +7 oxidation states, respectively, and has no unpaired electrons.
Manganate(
O4 2–) , Mn(25) = [Ar]3d64s2 Mn+6(25) = [Ar]3d1 Paramagnetic Permanganate (
O4-) Mn(25) = [Ar]3d64s2 Mn+7(25) = [Ar]3d0 Diamagnetic Option D : "Manganate and permanganate ions are tetrahedral." This statement is true.
Both manganate and permanganate ions have a tetrahedral geometry, with the manganese atom at the center and the four oxygen atoms surrounding it.
Therefore, the incorrect statement is option C.
In presence of luminous flame, blue cupric metaborate is reduced to colourless cuprous metaborate.
If non-luminous flame is present in reaction, cupric metaborate is obtained by heating boric anhydride with copper sulphate.
So, both statements are false.
Red colour of ruby is due to presence of (chromium ions), not (cobalt ions). in Al2O3.
Chromium is the trace element that causes ruby’s red colour, which ranges from an orange red to a publish red.
The strength of ruby’s red depends on how much chromium is present.
The +3 oxidation state of lanthanide is most stable and therefore lanthanide in +4 oxidation state has strong tendence to gain e– and converted into +3 and therefore act as strong oxidizing agent. eg Ce+4 And therefore CeO2 is used to oxidized alcohol aldehyde and ketones.
Lanthanide in +2 oxidation state has strong tendency to loss e– and converted into +3 oxidation state therefore act as strong reducing agent.
EuSO4 act as a strong reducing agent.
Cr+ [Ar]3d5 Mn2+ [Ar]3d5
Nd (60) = 4f4 6s2 Pr (59) = 4f3 6s2 Dy (66) = 4f10 6s2 Yb (70) = 4f14 6s2 Yb+2 has fully-filled 4f orbital, it will require very large amount of energy to reach +4 oxidation state.
Size of Bk3+ is 98 pm Size of Np3+ is 101 pm So size of Np3+ is more than Bk3+ ion. there is a gradual decrease in the size of M3+ ions across the series.
This may be referred to as the actinoid contraction.
FeI3 does not exist as I– reduces Fe3+ to Fe2+. 2Fe3+ + 2I – 2Fe2+ + I2.
(A)
In complex
There is no unpaired electron, so, m = 0 BM (B)
In complex,
There are 8 unpaired electrons.
(C)
In complex
contain six unpaired electrons. So,
Hence, order of spin only magnetic moment
.