Actinides and Lanthanides Chemistry Questions
Actinides and Lanthanides Chemistry Questions
(i) Cobalt (l1) is very stable in aqueous solutions but Atomic number
gets easily oxidised in the presence of strong Explain the reason why Cr has highest melting
ligands.
(ii) Actinoids exhibit a greater range of oxidation point and manganese (Mn) a lower melting p
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states than lanthanoids. All India 2014C
32. (i) Name twO OXometal anions of the 3d-sseriesofth
29. Compare the chemistry of the actinoids with that of transition metals in which the exhibits
lanthanoids with reference to the following: metal
Oxidation state equal to its group number.
() Electronic configuration (i) Oxidation states solutiot
(ii) What is the effect of
(iii) Chemical reactivity Delhi 2011C, 2010C of K,Cr,0,? increasing pH ona
153
BlockEElements
exhibits only
WhyisCu not stable in aqueous solution ?
(a) Transition metal of 3d-series that
37. (i)
Namea member of Lanthanoid series which is one oxidation state
as a
well- knownito exhibit +4 oxidation state of 3d-series that acts
(b) Transition metal +2 oxidation states
in
in
Nametwo elements of 3d-series
which
p)anomalous electronic configuration.
show strong reducing agent
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the following equation:
()4
Atransition element Xhas electronic (1) Complete and balance
Fe2+
configuration(Ar}4s3d3 Predict its likely (a) Cr,0% +14H* +6
Heat
Oxidation states.
(b) KMnO4 CBSE 2023
Complete the reaction mentioning allthe Write its one use.
()products formed. (111) What is Misch metal ? aqueous
ore (A) is fused with an
38. (1) When a chromite carbonate in free excess of air,
2KMnO, solution of sodium
compound (B) is obtained.
(m)
Account for the following. a yellow solution of acidified with
(a) Inthe 3d-transition series, zinc has the lowest This solution is filteredand Compound
enthalpy of atomisation. sulphuric acid to form compound (C).
KClgives orange
(C) on treatment with solution of chemical
the
h) Cu ion is unstable in aqueous solution. crystals of compound (D). Write
(c) Actinoids show more number of oxidation formulae of compounds A to D.
states than lanthanoids. following variations with
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(ii) Describe the cause of the actinoids:
. Write the number of unpaired electrons in Cr3+ respect to lanthanoids and
states of actinoids as
(Atomic number ofCr= 24) (a) Greater range of oxidation
compared to lanthanoids.
(i) Complete the reaction mentioning all the to
produces formed (b) Greater actinoid contraction as compared
lanthanoid contraction.
Cr,0% +3H,S+8H* (c) Lower ionisation enthalpy of early actinoids as
(iü) Account for the following compared to the early lanthanoids. CBSE SQP 2020
(a) Mn is more stable than Fe towards 39, (i) What happens, when
oxidation to +3 state. (a) manganate ions (Mn0 ) undergoes
disproportionation reaction in acidic
b) Copper hâs exceptionally positiveE o medium?
value.
(c) Eu with electronic configuration (b) lanthanum is heated with sulphur?
[Xe]4f'5d' 6s is a strong reducting agent. (ii) Explain the following trends in the properties
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elements.
35. () Account for the following. (a) EyM) value for copper is positive
/ Mn couple is much (+0.34 V) in contrast to the other members of
(a) E° value for Mn
/Cr2+ the series.
more positive than that for Cr
coloured in (b) Cr* is reducing while Mn is oxidising,
(b) Sc* is colourless whereas Ti* is
an aqueous solution. though both have d configuration.
oxidation states.
(c) Actinoids show wide range of (c) The oxidising power in the series increases
)Write the chemical equations for the preparation
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in the order: VO; <Cr,0 <Mn0,
of KMnO4 from MnO,. CBSE SQP 2020
K, (0) Account for the following. 40. (i) Account for the following.
(a) Transition metals form alloys. (a) Transition metals show variable oxidation
b)Cet+ IS a strong oxidising
agent. states.
(i) Wite One similarity and one difference chemistry (b) Zn, Cd and Hg are soft metals.
of lanthanoids andactinoids. (c) E value for the Mn/Mn* couple is highly
Complete the following ionic equation. positive (+ 1.57V) as compared to Cr*/Cr*.
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Cr,0 +2OH
Question Bank :
154
Chapterwise CBSE
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prepare
Howdo you
(i) Wnite one similarity and one difference between
43. (i)
Mn0,fromMnO,?
K,
the chemistrv of lanthanotd and actinoid
(a)
Na,Cr,0, from Na,CrO,?
elements.
AllIndio 2017 (b) following:
forthe
(i) Account morestable
than Fe
towards
41. () (a) How is the variability in oxidation states o (a) Mn is +3state.
transition metals different from that of the oxidation to
atomisation is
p-block elements?
(b) Out of Cu and Cu . which ion is unstable
(b) The enthalpy of
of the trans1tion
lowest
elemente for
in 3d-series
in aqueous solution and why? elements show wide range of
(c) Actinoid
(c) Orange colour ofCr,0: ion changes to Oxidation states. Delhi 2
yellow when treated with an alkali. Why? element of 3d-transition series
(ü) Chemistry of actinoids is complicated as compared
Delhi 2017
44. (i) Namethe
maximumnumber
of. oxidation
states. which
to lanthanoids. Give two reasons. shows
showso?
Why does it
42. (i) With reference to structural variability, chemical Whichtransition metal of33d-series has positive
reactivity, write the differences between (ü) Value andwhy?
lanthanoids and actinoids. Ey
(ii) Name a member of the lanthanoid series which is and Mn3+ which is a stronger
(iüi) Out of Cr why?
well known to exhibit + 4 oxidation state. oxidisingagentand
(ii) Complete the following equation. member ofthe lanthanoid series which is
(iv) Name a +2 Oxidation state
MnO; -8H´ + 5e wellknown to exhibit
following equation,
(iv) Out of Mn and Cr*, which is more (v) Complete the All India 2014
paramagnetic and why? MnO, +8H +5e
Explanations
is not the 6. The wide range of oxidation states of actinoids is
1. (b) Both (A)and (R)are correct but (R) attributed tothe fact that the 5 f,6d and 7s energy
moment is
corect explanation of (A). The magnetic levels are of comparable energies. Therefore, all
less
less as the 5f-electrons of actinoides are these three subshells can participate in bonding.
effectively shielded which result inquenching of But the most common oxidation state of actinoids is
orbital contribution. They are strongly paramagnetic also +3.
due to presence of unpaired electrons.
mixture 7. +2 and +4 oxidation states are also obtained due to
2. Lanthanoides are difficult to separate from high stabilities of f, f' and f configuration.
because of similarity in their physical and their
chemical properties. 8. Actinoids have lower ionisation energy and lesS
oxidation effective nuclear charge, hence more number of valen
3. Europium has half-filled f-orbital in +2
state. Thus, in lanthanoidseries, it exhibit +2 clectrons can take part in bond formation. It is due to
Oxidation state.
the fact that 5f,6d and 7s-levels are of comparable
energies. Therefore, actinojds exhibit +3,+4,+5,+0
4. Most common oxidation state of lanthanoid is +3. and +7 oxidation states due to the
5f,6d and 7s electrons in bond participat1on o
However. Ce shows +4, Eu and Yb show +2 oxidation
state because they acquire stable configuration.
actinoids exhibit greater range formation. Hence: that
of oxidation states
5. Due to lanthanoide contraction, the atomic radii of 4d lanthanoids.
and 5d-transition series elements are almost same. 9. Metallic radii of third (5d ) series of transition metals
That's why, Zr Z =40) and HÍ(Z=72 )have almost
identical radii. are virtually same as
because of the those of second (4d) series
lanthanoid contraction. Thls
d-ondf-Block Elements 155
Ce is (Xe ]4f'5d'. Since, Eu has half-filled 4f 23. (i) The electronic configuration of Co* and Cr* are
configuration, therefore, it is more stable than Ce* in [Ar]3d' and [Ar]3d respectively, since, they
which neither 4f nor Sd-subshell are half-filled or contain unpaired electrons and hence are coloured.
Completely filled. On the other hand,Se* having configuration
17. Refer to solution 10. [Ar]3d" does not contain any unpaired electrons
Consequences of lanthanoid contraction are and thus colourless in aqueous solution. (1)
1) With increase in atomic number, the basic strength (ii) Ea /Cu is positive, i.e. +034V because the sum
ofoxides and hydroxides of lanthanoids decreases. of enthalpies of sublimation and ionisation is not
(i) Elements of second and third d-series exhibit balanced by hydration enthalphy. (1)
Similar radii (e g. Zr-160 pm, Hf-159 pm) and have (ii) Due to lanthanoid contraction, the size of
very similar physical and chemical properties. (1) lanthanoid ion decreases regularly with increase in
. Comparison of lanthanods and actinoids atomic SIZe.
Therefore, the covalent nature of Ln-OH bond
Similarities increases from La to Lu. Hence, the basic
)Both have mainlyan oxidation state of +3
character of hydroxides decreases from La(OH), to
) Both show magnetic andspcctral properties Lu(OH),. Thus, La(OH), is more basic than
Lu(OH);: (1)
QUestion Bank:
156 Chapterwise CBSE
isOxidation
most common In
lanthanoids. +3
statesalongwith
CHEoxidatMioISnTR
+2 and + 4. While in
24. (i) Refer to (ii)
(ii) E°value solution
S6 (i) actinoids, there is a grcater range of oxidation
for (Mn2/ Mn)(Topic
1). (1)
aro
7s levels
is negative, 5/, 6d and show
(Cu*/Cu) is positive because whereas o states because They
in case of copper. comparable energies. and + 7 oxidation
the enthalpy of atomisation is very high 4, + 5,
+6 states.
actinoids is
hydration enthalpy is very low. The highwhile its +3, +
+2, oxidation state in +3.
energy to Common reactivity Lanthanoids are less reactive
(iii) Chemical
transform Cu(s) to Cu (ag) is not balanced by its
hydration enthalpy. (1) than actinoids.
Actually, earlier members of lanthanoids are
(11) Thcgeneral electronicconfiguration of actinoids
is Sfl-1640- [Link] reactive similar to calcium but with
iregularities in the quite
increasing atomic number, they behave
more like
clectronic configuration of actinoids is due to the
stabilities of f, f' and 4stable configuration of aluminium.
Lanthanoids react with dilute acids to liberate H.
5f-orbitals. (1) gas, while actinoids react with boiling water and
25. (1) Atoms of transition metal can easily take place in mixture of oxide and hydrogen gas.
gives a
the crystal lattice of another metal in the molten
Among the given options, Ti and Cu2+ ha
state andare miscible with cach other and thus 30. (i) 1 unpaired electron. Thus. their magnetic m
momen:
form alloys. (1)
(ii) With increase in the oxidation state of agiven is 1.73 or V3. sacrificial metals. As, it is
transition metal (i.e. Mn), the covalent character of (ii) Zinc can be used as
more reactive than iron and lose their electrons in
its compound increases and thus acidic character preference to iron. This prevent iron from losing iy
also increases. Therefore, Mn ,0, (oxidation state
oxidised.
= +3) is basic while Mn ,0, (oxidation state = +7) is electrons and becoming (u2
acidic. (1) Mn = 3d5 4,
(iii) Electronic configuration of
(ii) Eu 2* having electronic configuration [Xe14f is a Electronic configuration ofCr*
-3d5
strong reducing agent because in the aqueous As Cr has stable half-filled electronic
solution, it reverts back to the most stable +3
(1) configuration thus, it required more ionisation
oxidation state.
26. (i) Refer to solution 90 (i) (a) (Topic 1). energy to remove electron from stable
configuration. Whereas, Mn has l electron in 4
(ii) Refer tosolution 27 (Topic 1). and which can easily be removed. Thus, its
(iii) Refer to solution 8. (1x3)
have ionisation energy is less.
27. (i) (a) In actinoids, 5f-orbitals are filled which (iv) Sc in its common oxidation, i.e. (+2) state has no
more poor shielding effect than 4f-orbitals in
lanthanoids. Thus, the effective nuclear charge electron in 3d-orbitaland Zn has no unpaired
electron in its 3d-orbital.
experienced by electrons in valence shells in
case of actinoids is much more than that Thus, both Sc and Zn form colourless compound
experienced by lanthanoids. Hence, the size and are diamagnetic in nature.
contraction in actinoids is greater as compared (v) The radiiof trivalent and quadrivalent ions of
to that of lanthanoids. (1)
actinoids contract slightly with increasing atomt
(b) Refer to solution 31 (Topic 1). (1) number. This contraction is known as actinoid
(1) Refer to solution 6l (ii)(Topic 1). (1) contraction. This result from poor shielding
28, (i) Refer to solution 27 (Topic ). experienced by 5f-electrons.
(11) Refer to solution 52 (ii) (Topic 1). (vi) The oxidation state in chromate ion [Cr,0; Jand
(ii) Refer to solution 8.
dichromate ion [Cr,0; Jis +3 and t6 respectively
(|x3)
(10
29.(i) Electronic configuration (vii) 2Mn0, +101 +6H* ’2Mn * + 8H,0 +Sl; (13
Lanthanoids = |Xe]4/ 014 5 40 6s'
31. (i) Refer to (!
Actinoids =(Rn]5f 01 640 7s' (1) solution 11.
(ii) 3Mn0; +4H ’2MnO, + MnO, +2H,0
d-ond.f-Block Elements 157
K, MnO,+MnO, +0,
(a) 4FeCr,0, +8Na,C0, +70,
(i) 2KMnO, (4) 8Na,CrO4 + 2Fe,0, +8CO,
(Potasiun (Potassium
manganate) (1) (B)
permanganate)
(b) 2Na,CrO, +2H ’ Na,Cr,0, +2Na"
(üi) (a) Refer to solution 53(i) (Topic-1). (C) + H,0
(b) Refer to solution 34 (Topic-1). (c) Na,Cr,0, + 2KCI’K,Cr,0, + NaCI
(c) Refer tosolution 8. (3) (D)
corect answer out of the Mendeleev recognised that certain properties the
CHEMISTRY
basis of the above passagefollowing choices on the of some of of
CBSE Question Bank
(a) Both (A) and (R) are correct and (R) is
the correct
in Group VIIIare related to those
elements in Group VIl and those at the start of
elementa
the nex
explanation of (A). row Group I.
(b) Both (A) and (R) are correct but (R) is In that sense, these elements might be described as
not the correct
explanation of (A). transitional from one row of t
possessing properties the
(c) (A) is corTect and (R) is incorrect. table to the next.
(d) (A) is incorrect and (R) is correct. (1) Group 12 elements are not considered as transition
()) Assertion (A) Cations of transition elements occur in element because
various valence states (a) they have incomplete d-shell in ground state.
Reason (R) Large number of oxides of transition (b) they do not have incomplete d-shell in ground
elements are possible. state.
(ii) Assertion (A) Crystal structure of oxides of transition (c) they do not have complete d-shell excited state
metals often show defects. d-shell in excited sto
(d) they have incomplete
Reason (R) Ligand field effect cause distortions in elements in periodi
(ii) What is the place of d-block
crystal structures. table ?
(iii) Assertion (A) Transition metals form protective oxide (a) Group 3-12 (b) Group 4-13
films. (c) Group 3-13 (d) Group 3-11
periodic table
Reason (R) Oxides of transition metals are always (ii) Group VIIelements of Mendeleev
stoichiometric. belongs to
(iv) Assertion (A) CrO crystallises in a hexagonal (a) carbon family (b) transition elements
close-packed array of oxide ions with two out of every (c) boron family (d) halogen family
three octahedral holes occupied by chromium ions. (iv) Which is the correct electronic configuration of nickal
Reason (R)Transition metal oxide may be hexagonal (a) [Ar],g3d'4s? (b) [Ar];s 3d 462
close-packed lattice of oxide ions with metal ions (d) [Ar])g 3d° 452
filling the octahedral voids. (c) [Ar] 3dl° 4s!
Or
2. Readthe passage given below and answer the How many elements are present in d-block?
following questions. (a) 40 (b) 41 (c) 42 (d) 43
The d-block elements are the 40elements contained in
the four rows of ten columns (3-12) in the periodic 3. Read the passage given below and answer the following
table. As all the d block elements are metallic, the term questions.
d-block metals is synonymous. This set of d-block Transition metals combine with oxygen at high
elements is also often identified as the transition temperature to give metallic oxides. Except Sc, all the
metals, but somnetimes the group 12 elements (zinc, metals upto Mn form monoxide (MO), which are ionic
cadmium, mercury) are excluded from the transition in nature.
metals as the transition elements are defined as those As oxidation number increases, covalent nature and
with partly filled d orfshells in their compounds.
acidic character increases. In general, the oxides in
Inclusion of the elements zinc, cadmium and mercury lower oxidation states of metal are basic and in ther
is necessary as some properties of the group 12 higher oxidation states, they are acidic whereas in the
elements are appropriate logically to include with a intermediate oxidation state, the oxides are amphotet.
discussion of transition metal chemistry. The term
transition element or transition metal appeared to Behaviour of oxides of manganese
derive from early studies of periodicity such as the +2 + 8/3 +3 +4
Mendeleev periodic table of the elements. MnO Mn 0, Mn ,0, MnO,
Basic Mn ,0,
His horizontal table of the elements was an attempt to Acidic
Anphoteric (Covalent green oi)
group the elements together so that the chemistry of
elements might be explained and predicted. In this Basic oxides
table there are eight groups labelled I-VIIlwith each Sc ,O,. Tio, Ti,0,, VO, V,0,, MnO,
subdivided into A and B subgroups.
FeO, CuCO, CoO, Nio, Cu,0, CrO
O-ondf-Block Elements 161
(ü) (a) Ligand field effect cause distortions in crystal Cr,0 +14H* + 6e 2Cr* +7H,0
structures. The actual oxides structures, however, Ionic equations
generally show departures from regular lattice due (i) Reaction of K,Cr,0, with I
distortions caused by packing of ions of different
size. So, crystal structure of oxides of transition
Cr,0 + l4H* +6I’2Cr** +31, +7H,o
metals often show defects. (i) Reaction of K,Cr,0, with H,S
(ii) (c) When transition metals exposed to oxygen at Cr,0% + 8H* + 3H,S 20r* +3S +7H,0
low and intermediate temperatures form thin, Or
metals
protective oxide films. Oxides of transition (i) 2MnO, + 5C,0 + 16H*
deviate
range from metallic to semiconducting and
by both large and small degrees from stoichiometry.
2Mn* + 8H,0 + 10CO,
(iv) (d) The crystal structure of oxides in transition (i) Cr,0 (aq) +6Fe* (aq) +14H (aq)
metals are classified by considering a cubic or 2C,3+
+6Fe* +7H,0
ions
hexagonal closed packed lattice of one set of