Due to stable electronic configuration of Cr+1 ion (3d5)
d and f Block Elements
NOTE : The main reason for exhibiting larger number of oxidation states by actinoids as compared to lanthanoids is lesser energy difference between
and
orbitals as compared to that between
and
orbitals.
Lower oxidation state of an element forms more basic oxide and hydroxide, while the higher oxidation state will form more acidic oxide/hydroxide.
For example,
Most of the
compounds except
and
are coloured due to the presence of
-electrons.
The number stable oxidation states of lanthanides is
.
Colour of Fe2+ is observed green and Fe3+ is yellow.
charge transfer spectra.
is colored because it absorbs light in the visible range of electromagnetic radiation.
The permanganate ion is the source of color, as a ligand to metal,
charge transfer takes place between oxygen's
orbitals and the empty
-orbitals on the metal.
This charge transfer takes place when a photon of light is absorbed, which leads to the purple color of the compound.
On addition of impurities to the colourless gemstones, brilliant colours are produced.
On addition of chromium to colourless corundum (Al2O3), a red ruby is formed.
Red colour ruby is obtained when Cr3+ ions replace Al3+ ions in the octahedral sites of corundum.
A green emerald emerges when chromium is added to colourless beryl (Be3Al2(SiO3)6).
Green colour emerald is obtained when Cr3+ ions replace Al3+ in the octahedral site of beryl.
Out of all the four given metallic oxides
is attracted by magnetic field very strongly. The effect persists even when the magnetic field is removed. Thus
is metallic and ferromagnetic in nature.
Cu2+ and Ni2+ ions belong to Group II and Group IV respectively.
Group II sulphides precipitated out even under low concentration of sulphides, while Group IV sulphides require higher concentration of sulphides.
To fulfill this reaction condition, dil.
HCl is chosen in Group II reagents and NH4OH is chosen in Group IV reagents.