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3 Explain the relatively small changes in atomic radii, ionic radii and ionization energies across the period.
Transition elements are elements found in the d-block which form one or more single ions with an incomplete d electron sub-shell. First row transition elements are the ones circled in red:
Although Scandium and Zinc are block elements, they are not transition elements. Scandium forms only one ion Sc3+ , with no electrons in its d subshell. Zinc forms only one ion, Zn2+ and has a complete 3d sub-shell. The electronic configuration for Copper (and Chromium) do not follow pattern when filling the sub-shell. For copper(Cu), the arrangement of a d sub-shell with paired electrons in each orbital, [Ar]3d104s1, gives greater stability than having one of the d orbitals with only a single electron in it.
The electronic configuration of transition metals is special in the sense that they can be found in numerous oxidation states. Although the elements can display many different oxidation states, they usually exhibit a common oxidation state depending on what makes that element most stable. In the first row of the transition metals, the ten elements that can be found are Titanium (Ti), Vanadium (V), Chromium (Cr), Manganese (Mn), Iron (Fe), Cobalt (Co), Nickel (Ni) and Copper (Cu).
Oxidation States
Element Symbol
Ti V Cr
Atomic Number
22 23 24
+1
+2
+3
+4
+5
+6
+7
No
Rare
No No Common
No No No
Mn
25
Common
Common (purple)
Fe
Co
26
27
Common (ferric)
Common
Rare
Rare
Rare
Rare
Rare
Rare
No
No
Ni
Cu
28
29
Rare Common
Rare Common (blue/green )
Rare
No
Rare
No
No
No
No
No
No
No
The decrease in atomic radii from left to right across the first row of the d-block is small and irregular. The decrease is much less than that seen on moving across a short period such as sodium to argon. In the first row of the d block, as the nuclear charge increases across the period, each additional electron enters the penultimate 3d orbital which increases the shielding experienced by the 4s electrons. This results in a relatively small difference in the effective nuclear charge as the shielding effect nullifies, to a large extent, the increase in nuclear charge.
The ionic radii, like the atomic radii tend to increase along the series but only slightly as compared with the large differences in the s an p block elements. The increased attractive effect of the nucleus on the outer electrons from one transition element to the next is almost cancelled by the increased repulsive forces caused by the extra repulsion of the 3d electrons.
The first ionisation energy increases from left to right across the first row of the d block. However the increase is relatively small compared to that of the short period sodium to argon. In the first row of the d block, as the nuclear charge increases each additional electron enters the penultimate 3d orbitals. These 3d electrons efficiently shields the 4s electrons from the nucleus. Thus the increased nuclear attraction for the outer 4s electrons is minimal across the period. This results in relatively small changes in the energy required to remove an outer 4s electron.
Ti 0.132
V 648
Cr 653
Mn 716
Fe 762
Co 757
Ni 736
Cu 745
0.090
0.090
0.085
0.080
0.076
0.078
0.078
0.069
661
648
653
716
762
757
736
745