1 . Describe the chemistry of the group 14 elements with
reference to (i) decreasing
catenation, (ii) increased metallic behaviour on descending the
group and (iii) the relative
stability of the +2 and +4 oxidation states.
2. Discuss with relevant examples how the stability of the +2
oxidation state varies across
the 1st row transition metals. Describe with relevant examples the
general types of
ligands that can stabilise higher oxidation states in metal
complexes.
3. Discuss in detail the spectroscopic techniques used to
examine toxic metal concentration
in the human body and how these techniques are applied.
please answer all
Group 14 elements are C Si Ge Sn Pb.
1. catenation is the property of element to bond itself through covalent bond
The order of catenation property is:
C >> Si > Ge >> Sn > Pb.
Catenation is the property of non-metal having small size. As we move down group, size increases. Due to this bond trength decreases. hence bonding property of element decreases as a result catenation decreases
2. Metallic character is due to the fotrmation iof metal cation by loosing electrons, Metals has property to lose electrons in chemical reactions.
As we move down the group, there is less shielding of electrons by the nucleus or weaker nucleus attraction hence the tendency to remove electron increases.Thererfore metallic charcter increases.
3. Oxidation means loss of electrons .
Oxidation state +2 and +4
General electronic configuration of 14 the group is ns2np2 . That means 4 valence electrons.
by loosing 2 electrons the element is left with filled ns2 orbitals. We know half filled and fully filled orbitals provide extra stability. Thus +2 is stable oxidation state. (innert pair effect also work)
By loosing 4 electrons the element has lost all of its valence elctrons and achived stable noble gas configuration. This provide extra stability to the element in +4 oxidation state. Thus +4 is stable oxidation state.
1 . Describe the chemistry of the group 14 elements with reference to (i) decreasing catenation,...
1 (i) Discuss how the nature of the ligand, position of the metal in the d-block elements and metal oxidation state influence the magnitude of the d orbital splitting in metal complexes, (as applied in crystal field theory). Outline the principal differences between the 1st row and 2nd/3rd row transition metal complexes. (ii) Describe with relevant examples and diagrams the several types of isomerism which are commonly encountered in transition metal complexes.