D F Block Elements

d & f block elements
d -Block elements:
The elements lying in the middle of periodic table belonging to
groups 3 to 12 are known as d – block elements.
Their general electronic configuration is (n – 1)d1-10 ns1-2 where (n
– 1) stands for penultimate (last but one) shell.
Transition element:
A transition element is defined as the one which has
incompletely filled d orbitals in its ground state or in any one of
its oxidation states.
Zinc, cadmium, mercury are not regarded as transition metals
due to completely filled d – orbital.
f-Block elements:
The elements constituting the f -block are those in which the 4 f
and 5 f orbitals are progressively filled in the latter two long
Four transition series
a. 3d – transition series.
The transition elements with atomic number 21(Sc) to 30(Zn) and having
incomplete 3d orbitals is called the first transition series.
b. 4d – transition series.
It consists of elements with atomic number 39(Y) to 48 (Cd) and having
incomplete 4d orbitals. It is called second transition series.
c. 5d – transition series.
It consists of elements with atomic number 57(La), 72(Hf) to 80(Hg) having
incomplete 5d orbitals. It is called third transition series.
d. 6d – transition series.
It consists of elements with atomic number 89(Ac), 104(Rf) to 112(Uub)
having incomplete 6d orbitals. It is called fourth transition series
General Characteristics of transition
elements
• a. Metallic character:
All transition elements are metallic in nature, i.e. they have
strong metallic bonds. This is because of presence of unpaired
electrons. This gives rise to properties like high density, high
enthalpies of atomization, and high melting and boiling points.
• b. Atomic radii:
The atomic radii decrease from Sc to Cr because the effective
nuclear charge increases. The atomic size of Fe, Co, Ni is almost
same because the attraction due to increase in nuclear charge is
cancelled by the repulsion because of increase in shielding effect.
Cu and Zn have bigger size because the shielding effect increases
and electron electron repulsions repulsion increases
Melting point and boiling point
c. Ionisation enthalpy: There is slight and irregular
variation in ionization energies of transition metals
due to irregular variation of atomic size. The I.E. of
5d transition series is higher than 3d and 4d
transition series because of Lanthanoid Contraction
VARIATION IN IONISATION ENTHALPY
• With the filling of (n - 1) d orbitals effective nuclear charge

increases
resulting in the increase in first ionisation enthalpy.
There are some irregular variations.
• The first ionisation enthalpy of chromium is lower because
the removal of one electron produces extra stable d5
configuration and that of zinc is higher because the removal
of electron takes place from fully filled 4s orbital.
• Second ionization enthalpy of Zn is lower than second
ionization enthalpy of Cu (1958 kj/mol). This is because
removal of second electron in Zn produces stable d10
configuration while the removal of second electron in Cu
disrupts the d10 configuration with a considerable loss in
exchange energy to from less stable d9 configuration.
Cr = 3d5 4s1
Zn = 3d10 4s2; Zn2+ = 3d10
Cu = 3d10 4s1; Cu2+ = 3d9
• Oxidation state: Transition metals show variable
oxidation states due to tendency of (n-1) d as well
as ns electrons to take part in bond formation.
• Magnetic properties:
Most of transition metals are paramagnetic in
nature due to presence of unpaired electrons. It
increase s from Sc to Cr and then decreases because
number of unpaired and then decrease because
number of unpaired electrons increases from Sc to
Cr and then decreases.
Catalytic properties
Most of transition metals are used as catalyst
because of
(i) presence of incomplete or empty d –
orbitals,
(ii) large surface area,
(iii) variable oxidation states
(iv) ability to form complexes, e.g., Fe, Ni, V2O3,
Pt, Mo, Co and used as catalyst.
• Formation of coloured compounds:
They form coloured ions due to presence of
incompletely filled d – orbitals and unpaired
electrons, they can undergo d – d transition by
absorbing colour from visible region and radiating
complementary colour.
• Formation of complexes:
Transition metals form complexes due to
(i) presence of vacant d – orbitals of suitable energy
(ii) smaller size
(iii) higher charge on cations.
Interstitial compounds:
Transition metals have voids or interstitials in which
C, H, N, B etc. can fit into resulting in formation of
interstitial compounds. They are non – stoichiometric,
i.e., their composition is not fixed, e.g., steel. They are
harder and less malleable and ductile.
Alloys formation:
They form alloys due to similar ionic size. Metals can
replace each other in crystal lattice, e.g., brass,
bronze, steel etc
PREPARATION AND PROPERTIES OF K2Cr2O7
• It is prepared by fusion of chromate ore (FeCr2O4) with sodium

carbonate in excess of air.
4FeCr2O4 + 8Na2CO3 + 7O2 8Na2CrO4 + 2Fe2O3 + 8CO2
2Na2CrO4 + H2SO4 Na2Cr2O7 + H2O + Na2SO4
Na2Cr2O7 + 2KCl K2Cr2O7 + 2NaCl

Structures of Chromates and dichromates
Reactions of Potassium dichromate
Acidified K2Cr2O7 oxidises iodides to iodine,
sulphides to sulphur, tin (ll) to tin (IV).
Preparation of Potassium permanganate
• Potassium permanganate is prepared by fusion of MnO4

with alkali metal hydroxide (KOH) in presence of O2 or
oxidising agent like KNO3. It produces dark green
K2MnO4 which undergoes oxidation as well as reduction
in neutral or acidic solution to give permanganate.
Or
• Commercially it is prepared by the alkaline oxidative
fusion of MnO2 followed by the electrolytic oxidation of
manganate (Vl)
LANTHANOID CONTRACTION AND ITS CONSEQUENCE
• The 4f orbitals screen the nuclear charge less effectively

because they are large and diffused. The filling of 4f
orbitals before 5d orbitals results in the gradual increase
in effective nuclear charge resulting in a regular decrease
in atomic and ionic radii. This phenomenon is called
lanthanoid contraction.
• The corresponding members of second and third
transition series have similar radii because the normal
size increase down the group of d-block elements almost
exactly balanced by the lanthanoid contraction.
Properties of KMnO4
• KMnO4acts as strong oxidising agent.
In the presence of dilute H2SO4, KMnO4 is reduced
to manganous salt.
• Acidic KMnO4 solution oxidises oxalates to CO2,
iron(II) to iron (lll), nitrites to nitrates and iodides
to iodine. The half-reactions of reductants are
In alkaline medium, KMnO4 is reduced to
insoluble MnO2.
Baeyer’s reagent structures
Oxidation States of Lanthanoids and Actinoids
• The most common and most stable oxidation state of

lanthanoids is +3. They also show oxidation states of +2, and
+4 .
The corresponding lanthanoid ions have extra stable 4f 0, 4f7
and 4f14 configuration.
Ce4+ + e– Ce3+, + 3 more stable O.S. than + 4
Tb2+ + e– Tb3+, + 3 more stable O.S. than + 4
Hence Ce4+ and Tb4+ are strong oxidants.
Eu2+ Eu3+ + e–, +3 more stable O.S. than +2
Yb2+ Yb3+ + e–, + 3 more stable O.S. than + 3
Hence, Eu2+ and Yb2+ are strong reducing agents.
Properties of Lanthanoids and Actinoids
Lanthanoids Actinoids
+3 oxidation state is most
common along with +2 and +4 Actiniods also show higher
oxidation states such as +4, +5,
Except Promethium, they are
+6 and +7. They are more
non-radioactive.
reactive
The magnetic properties of
They are radioactive
lanthanoids are less complex
than actinoids.
The magnetic properties of the
actinoids are more complex than
those of the lanthanoids

D F Block Elements

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d & f block elements

• With the filling of (n - 1) d orbitals effective nuclear charge

• It is prepared by fusion of chromate ore (FeCr2O4) with sodium

4FeCr2O4 + 8Na2CO3 + 7O2 8Na2CrO4 + 2Fe2O3 + 8CO2

2Na2CrO4 + H2SO4 Na2Cr2O7 + H2O + Na2SO4

Na2Cr2O7 + 2KCl K2Cr2O7 + 2NaCl

• Potassium permanganate is prepared by fusion of MnO4

• The 4f orbitals screen the nuclear charge less effectively

• The most common and most stable oxidation state of

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