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1 | 4305-4308 | 10 Table 4 10: Some Properties of Actinium and Actinoids
Electronic conifigurations*
Radii/pm
Atomic
Name
Symbol
M
M
3+
M
4+
M
3+
M
4+
Number
89
Actinium
Ac
6d
17s
2
5f
0
111
90
Thorium
Th
6d
27s
2
5f
1
5f
0
99
91
Protactinium
Pa
5f
26d
17s
2
5f
2
5f
1
96
92
Uranium
U
5f
36d
17s
2
5f
3
5f
2
103
93
93
Neptunium
Np
5f
46d
17s
2
5f
4
5f
3
101
92
94
Plutonium
Pu
5f
67s
2
5f
5
5f
4
100
90
95
Americium
Am
5f
77s
2
5f
6
5f
5
99
89
96
Curium
Cm
5f
76d
17s
2
5f
7
5f
6
99
88
97
Berkelium
Bk
5f
97s
2
5f
8
5f
7
98
87
98
Californium
Cf
5f
107s
2
5f
9
5f
8
98
86
99
Einstenium
Es
5f
117s
2
5f
10
5f
9
–
–
100
Fermium
Fm
5f
127s
2
5f
11
5f
10
–
–
101
Mendelevium
Md
5f
137s
2
5f
12
5f
11
–
–
102
Nobelium
No
5f
147s
2
5f
13
5f
12
–
–
103
Lawrencium
Lr
5f
146d
17s
2
5f
14
5f
13
–
–
Fig 4 7: Chemical reactions of the lanthanoids |
1 | 4306-4309 | Table 4 10: Some Properties of Actinium and Actinoids
Electronic conifigurations*
Radii/pm
Atomic
Name
Symbol
M
M
3+
M
4+
M
3+
M
4+
Number
89
Actinium
Ac
6d
17s
2
5f
0
111
90
Thorium
Th
6d
27s
2
5f
1
5f
0
99
91
Protactinium
Pa
5f
26d
17s
2
5f
2
5f
1
96
92
Uranium
U
5f
36d
17s
2
5f
3
5f
2
103
93
93
Neptunium
Np
5f
46d
17s
2
5f
4
5f
3
101
92
94
Plutonium
Pu
5f
67s
2
5f
5
5f
4
100
90
95
Americium
Am
5f
77s
2
5f
6
5f
5
99
89
96
Curium
Cm
5f
76d
17s
2
5f
7
5f
6
99
88
97
Berkelium
Bk
5f
97s
2
5f
8
5f
7
98
87
98
Californium
Cf
5f
107s
2
5f
9
5f
8
98
86
99
Einstenium
Es
5f
117s
2
5f
10
5f
9
–
–
100
Fermium
Fm
5f
127s
2
5f
11
5f
10
–
–
101
Mendelevium
Md
5f
137s
2
5f
12
5f
11
–
–
102
Nobelium
No
5f
147s
2
5f
13
5f
12
–
–
103
Lawrencium
Lr
5f
146d
17s
2
5f
14
5f
13
–
–
Fig 4 7: Chemical reactions of the lanthanoids Rationalised 2023-24
112
Chemistry
The actinoids are radioactive elements and the earlier members have
relatively long half-lives, the latter ones have half-life values ranging from
a day to 3 minutes for lawrencium (Z =103) |
1 | 4307-4310 | 10: Some Properties of Actinium and Actinoids
Electronic conifigurations*
Radii/pm
Atomic
Name
Symbol
M
M
3+
M
4+
M
3+
M
4+
Number
89
Actinium
Ac
6d
17s
2
5f
0
111
90
Thorium
Th
6d
27s
2
5f
1
5f
0
99
91
Protactinium
Pa
5f
26d
17s
2
5f
2
5f
1
96
92
Uranium
U
5f
36d
17s
2
5f
3
5f
2
103
93
93
Neptunium
Np
5f
46d
17s
2
5f
4
5f
3
101
92
94
Plutonium
Pu
5f
67s
2
5f
5
5f
4
100
90
95
Americium
Am
5f
77s
2
5f
6
5f
5
99
89
96
Curium
Cm
5f
76d
17s
2
5f
7
5f
6
99
88
97
Berkelium
Bk
5f
97s
2
5f
8
5f
7
98
87
98
Californium
Cf
5f
107s
2
5f
9
5f
8
98
86
99
Einstenium
Es
5f
117s
2
5f
10
5f
9
–
–
100
Fermium
Fm
5f
127s
2
5f
11
5f
10
–
–
101
Mendelevium
Md
5f
137s
2
5f
12
5f
11
–
–
102
Nobelium
No
5f
147s
2
5f
13
5f
12
–
–
103
Lawrencium
Lr
5f
146d
17s
2
5f
14
5f
13
–
–
Fig 4 7: Chemical reactions of the lanthanoids Rationalised 2023-24
112
Chemistry
The actinoids are radioactive elements and the earlier members have
relatively long half-lives, the latter ones have half-life values ranging from
a day to 3 minutes for lawrencium (Z =103) The latter members could be
prepared only in nanogram quantities |
1 | 4308-4311 | 7: Chemical reactions of the lanthanoids Rationalised 2023-24
112
Chemistry
The actinoids are radioactive elements and the earlier members have
relatively long half-lives, the latter ones have half-life values ranging from
a day to 3 minutes for lawrencium (Z =103) The latter members could be
prepared only in nanogram quantities These facts render their study
more difficult |
1 | 4309-4312 | Rationalised 2023-24
112
Chemistry
The actinoids are radioactive elements and the earlier members have
relatively long half-lives, the latter ones have half-life values ranging from
a day to 3 minutes for lawrencium (Z =103) The latter members could be
prepared only in nanogram quantities These facts render their study
more difficult All the actinoids are believed to have the electronic configuration of 7s
2
and variable occupancy of the 5f and 6d subshells |
1 | 4310-4313 | The latter members could be
prepared only in nanogram quantities These facts render their study
more difficult All the actinoids are believed to have the electronic configuration of 7s
2
and variable occupancy of the 5f and 6d subshells The fourteen electrons
are formally added to 5f, though not in thorium (Z = 90) but from Pa
onwards the 5f orbitals are complete at element 103 |
1 | 4311-4314 | These facts render their study
more difficult All the actinoids are believed to have the electronic configuration of 7s
2
and variable occupancy of the 5f and 6d subshells The fourteen electrons
are formally added to 5f, though not in thorium (Z = 90) but from Pa
onwards the 5f orbitals are complete at element 103 The irregularities in
the electronic configurations of the actinoids, like those in the lanthanoids
are related to the stabilities of the f
0, f
7 and f
14 occupancies of the 5f
orbitals |
1 | 4312-4315 | All the actinoids are believed to have the electronic configuration of 7s
2
and variable occupancy of the 5f and 6d subshells The fourteen electrons
are formally added to 5f, though not in thorium (Z = 90) but from Pa
onwards the 5f orbitals are complete at element 103 The irregularities in
the electronic configurations of the actinoids, like those in the lanthanoids
are related to the stabilities of the f
0, f
7 and f
14 occupancies of the 5f
orbitals Thus, the configurations of Am and Cm are [Rn] 5f
77s
2 and
[Rn] 5f
76d
17s
2 |
1 | 4313-4316 | The fourteen electrons
are formally added to 5f, though not in thorium (Z = 90) but from Pa
onwards the 5f orbitals are complete at element 103 The irregularities in
the electronic configurations of the actinoids, like those in the lanthanoids
are related to the stabilities of the f
0, f
7 and f
14 occupancies of the 5f
orbitals Thus, the configurations of Am and Cm are [Rn] 5f
77s
2 and
[Rn] 5f
76d
17s
2 Although the 5f orbitals resemble the 4f orbitals in their
angular part of the wave-function, they are not as buried as 4f orbitals
and hence 5f electrons can participate in bonding to a far greater extent |
1 | 4314-4317 | The irregularities in
the electronic configurations of the actinoids, like those in the lanthanoids
are related to the stabilities of the f
0, f
7 and f
14 occupancies of the 5f
orbitals Thus, the configurations of Am and Cm are [Rn] 5f
77s
2 and
[Rn] 5f
76d
17s
2 Although the 5f orbitals resemble the 4f orbitals in their
angular part of the wave-function, they are not as buried as 4f orbitals
and hence 5f electrons can participate in bonding to a far greater extent The general trend in lanthanoids is observable in the actinoids as well |
1 | 4315-4318 | Thus, the configurations of Am and Cm are [Rn] 5f
77s
2 and
[Rn] 5f
76d
17s
2 Although the 5f orbitals resemble the 4f orbitals in their
angular part of the wave-function, they are not as buried as 4f orbitals
and hence 5f electrons can participate in bonding to a far greater extent The general trend in lanthanoids is observable in the actinoids as well There is a gradual decrease in the size of atoms or M
3+ ions across the
series |
1 | 4316-4319 | Although the 5f orbitals resemble the 4f orbitals in their
angular part of the wave-function, they are not as buried as 4f orbitals
and hence 5f electrons can participate in bonding to a far greater extent The general trend in lanthanoids is observable in the actinoids as well There is a gradual decrease in the size of atoms or M
3+ ions across the
series This may be referred to as the actinoid contraction (like lanthanoid
contraction) |
1 | 4317-4320 | The general trend in lanthanoids is observable in the actinoids as well There is a gradual decrease in the size of atoms or M
3+ ions across the
series This may be referred to as the actinoid contraction (like lanthanoid
contraction) The contraction is, however, greater from element to element
in this series resulting from poor shielding by 5f electrons |
1 | 4318-4321 | There is a gradual decrease in the size of atoms or M
3+ ions across the
series This may be referred to as the actinoid contraction (like lanthanoid
contraction) The contraction is, however, greater from element to element
in this series resulting from poor shielding by 5f electrons There is a greater range of oxidation states, which is in part attributed to
the fact that the 5f, 6d and 7s levels are of comparable energies |
1 | 4319-4322 | This may be referred to as the actinoid contraction (like lanthanoid
contraction) The contraction is, however, greater from element to element
in this series resulting from poor shielding by 5f electrons There is a greater range of oxidation states, which is in part attributed to
the fact that the 5f, 6d and 7s levels are of comparable energies The
known oxidation states of actinoids are listed in Table 4 |
1 | 4320-4323 | The contraction is, however, greater from element to element
in this series resulting from poor shielding by 5f electrons There is a greater range of oxidation states, which is in part attributed to
the fact that the 5f, 6d and 7s levels are of comparable energies The
known oxidation states of actinoids are listed in Table 4 11 |
1 | 4321-4324 | There is a greater range of oxidation states, which is in part attributed to
the fact that the 5f, 6d and 7s levels are of comparable energies The
known oxidation states of actinoids are listed in Table 4 11 The actinoids show in general +3 oxidation state |
1 | 4322-4325 | The
known oxidation states of actinoids are listed in Table 4 11 The actinoids show in general +3 oxidation state The elements, in the
first half of the series frequently exhibit higher oxidation states |
1 | 4323-4326 | 11 The actinoids show in general +3 oxidation state The elements, in the
first half of the series frequently exhibit higher oxidation states For example,
the maximum oxidation state increases from +4 in Th to +5, +6 and +7
respectively in Pa, U and Np but decreases in succeeding elements (Table
4 |
1 | 4324-4327 | The actinoids show in general +3 oxidation state The elements, in the
first half of the series frequently exhibit higher oxidation states For example,
the maximum oxidation state increases from +4 in Th to +5, +6 and +7
respectively in Pa, U and Np but decreases in succeeding elements (Table
4 11) |
1 | 4325-4328 | The elements, in the
first half of the series frequently exhibit higher oxidation states For example,
the maximum oxidation state increases from +4 in Th to +5, +6 and +7
respectively in Pa, U and Np but decreases in succeeding elements (Table
4 11) The actinoids resemble the lanthanoids in having more compounds
in +3 state than in the +4 state |
1 | 4326-4329 | For example,
the maximum oxidation state increases from +4 in Th to +5, +6 and +7
respectively in Pa, U and Np but decreases in succeeding elements (Table
4 11) The actinoids resemble the lanthanoids in having more compounds
in +3 state than in the +4 state However, +3 and +4 ions tend to hydrolyse |
1 | 4327-4330 | 11) The actinoids resemble the lanthanoids in having more compounds
in +3 state than in the +4 state However, +3 and +4 ions tend to hydrolyse Because the distribution of oxidation states among the actinoids is so
uneven and so different for the former and later elements, it is unsatisfactory
to review their chemistry in terms of oxidation states |
1 | 4328-4331 | The actinoids resemble the lanthanoids in having more compounds
in +3 state than in the +4 state However, +3 and +4 ions tend to hydrolyse Because the distribution of oxidation states among the actinoids is so
uneven and so different for the former and later elements, it is unsatisfactory
to review their chemistry in terms of oxidation states 4 |
1 | 4329-4332 | However, +3 and +4 ions tend to hydrolyse Because the distribution of oxidation states among the actinoids is so
uneven and so different for the former and later elements, it is unsatisfactory
to review their chemistry in terms of oxidation states 4 6 |
1 | 4330-4333 | Because the distribution of oxidation states among the actinoids is so
uneven and so different for the former and later elements, it is unsatisfactory
to review their chemistry in terms of oxidation states 4 6 1 Electronic
Configurations
4 |
1 | 4331-4334 | 4 6 1 Electronic
Configurations
4 6 |
1 | 4332-4335 | 6 1 Electronic
Configurations
4 6 2 Ionic Sizes
4 |
1 | 4333-4336 | 1 Electronic
Configurations
4 6 2 Ionic Sizes
4 6 |
1 | 4334-4337 | 6 2 Ionic Sizes
4 6 3 Oxidation
States
The actinoid metals are all silvery in appearance but display
a variety of structures |
1 | 4335-4338 | 2 Ionic Sizes
4 6 3 Oxidation
States
The actinoid metals are all silvery in appearance but display
a variety of structures The structural variability is obtained
due to irregularities in metallic radii which are far greater
than in lanthanoids |
1 | 4336-4339 | 6 3 Oxidation
States
The actinoid metals are all silvery in appearance but display
a variety of structures The structural variability is obtained
due to irregularities in metallic radii which are far greater
than in lanthanoids 4 |
1 | 4337-4340 | 3 Oxidation
States
The actinoid metals are all silvery in appearance but display
a variety of structures The structural variability is obtained
due to irregularities in metallic radii which are far greater
than in lanthanoids 4 6 |
1 | 4338-4341 | The structural variability is obtained
due to irregularities in metallic radii which are far greater
than in lanthanoids 4 6 4 General
Characteristics
and Comparison
with Lanthanoids
Ac
Th
Pa
U
Np
Pu
Am
Cm
Bk
Cf
Es
Fm
Md
No
Lr
3
3
3
3
3
3
3
3
3
3
3
3
3
3
4
4
4
4
4
4
4
4
5
5
5
5
5
6
6
6
6
7
7
Table 4 |
1 | 4339-4342 | 4 6 4 General
Characteristics
and Comparison
with Lanthanoids
Ac
Th
Pa
U
Np
Pu
Am
Cm
Bk
Cf
Es
Fm
Md
No
Lr
3
3
3
3
3
3
3
3
3
3
3
3
3
3
4
4
4
4
4
4
4
4
5
5
5
5
5
6
6
6
6
7
7
Table 4 11: Oxidation States of Actinium and Actinoids
Rationalised 2023-24
113
The d- and f- Block Elements
The actinoids are highly reactive metals, especially when finely divided |
1 | 4340-4343 | 6 4 General
Characteristics
and Comparison
with Lanthanoids
Ac
Th
Pa
U
Np
Pu
Am
Cm
Bk
Cf
Es
Fm
Md
No
Lr
3
3
3
3
3
3
3
3
3
3
3
3
3
3
4
4
4
4
4
4
4
4
5
5
5
5
5
6
6
6
6
7
7
Table 4 11: Oxidation States of Actinium and Actinoids
Rationalised 2023-24
113
The d- and f- Block Elements
The actinoids are highly reactive metals, especially when finely divided The action of boiling water on them, for example, gives a mixture of oxide
and hydride and combination with most non metals takes place at
moderate temperatures |
1 | 4341-4344 | 4 General
Characteristics
and Comparison
with Lanthanoids
Ac
Th
Pa
U
Np
Pu
Am
Cm
Bk
Cf
Es
Fm
Md
No
Lr
3
3
3
3
3
3
3
3
3
3
3
3
3
3
4
4
4
4
4
4
4
4
5
5
5
5
5
6
6
6
6
7
7
Table 4 11: Oxidation States of Actinium and Actinoids
Rationalised 2023-24
113
The d- and f- Block Elements
The actinoids are highly reactive metals, especially when finely divided The action of boiling water on them, for example, gives a mixture of oxide
and hydride and combination with most non metals takes place at
moderate temperatures Hydrochloric acid attacks all metals but most are
slightly affected by nitric acid owing to the formation of protective oxide
layers; alkalies have no action |
1 | 4342-4345 | 11: Oxidation States of Actinium and Actinoids
Rationalised 2023-24
113
The d- and f- Block Elements
The actinoids are highly reactive metals, especially when finely divided The action of boiling water on them, for example, gives a mixture of oxide
and hydride and combination with most non metals takes place at
moderate temperatures Hydrochloric acid attacks all metals but most are
slightly affected by nitric acid owing to the formation of protective oxide
layers; alkalies have no action The magnetic properties of the actinoids are more complex than those
of the lanthanoids |
1 | 4343-4346 | The action of boiling water on them, for example, gives a mixture of oxide
and hydride and combination with most non metals takes place at
moderate temperatures Hydrochloric acid attacks all metals but most are
slightly affected by nitric acid owing to the formation of protective oxide
layers; alkalies have no action The magnetic properties of the actinoids are more complex than those
of the lanthanoids Although the variation in the magnetic susceptibility
of the actinoids with the number of unpaired 5 f electrons is roughly
parallel to the corresponding results for the lanthanoids, the latter have
higher values |
1 | 4344-4347 | Hydrochloric acid attacks all metals but most are
slightly affected by nitric acid owing to the formation of protective oxide
layers; alkalies have no action The magnetic properties of the actinoids are more complex than those
of the lanthanoids Although the variation in the magnetic susceptibility
of the actinoids with the number of unpaired 5 f electrons is roughly
parallel to the corresponding results for the lanthanoids, the latter have
higher values It is evident from the behaviour of the actinoids that the ionisation
enthalpies of the early actinoids, though not accurately known, but are
lower than for the early lanthanoids |
1 | 4345-4348 | The magnetic properties of the actinoids are more complex than those
of the lanthanoids Although the variation in the magnetic susceptibility
of the actinoids with the number of unpaired 5 f electrons is roughly
parallel to the corresponding results for the lanthanoids, the latter have
higher values It is evident from the behaviour of the actinoids that the ionisation
enthalpies of the early actinoids, though not accurately known, but are
lower than for the early lanthanoids This is quite reasonable since it is to
be expected that when 5f orbitals are beginning to be occupied, they will
penetrate less into the inner core of electrons |
1 | 4346-4349 | Although the variation in the magnetic susceptibility
of the actinoids with the number of unpaired 5 f electrons is roughly
parallel to the corresponding results for the lanthanoids, the latter have
higher values It is evident from the behaviour of the actinoids that the ionisation
enthalpies of the early actinoids, though not accurately known, but are
lower than for the early lanthanoids This is quite reasonable since it is to
be expected that when 5f orbitals are beginning to be occupied, they will
penetrate less into the inner core of electrons The 5f electrons, will therefore,
be more effectively shielded from the nuclear charge than the 4f electrons
of the corresponding lanthanoids |
1 | 4347-4350 | It is evident from the behaviour of the actinoids that the ionisation
enthalpies of the early actinoids, though not accurately known, but are
lower than for the early lanthanoids This is quite reasonable since it is to
be expected that when 5f orbitals are beginning to be occupied, they will
penetrate less into the inner core of electrons The 5f electrons, will therefore,
be more effectively shielded from the nuclear charge than the 4f electrons
of the corresponding lanthanoids Because the outer electrons are less
firmly held, they are available for bonding in the actinoids |
1 | 4348-4351 | This is quite reasonable since it is to
be expected that when 5f orbitals are beginning to be occupied, they will
penetrate less into the inner core of electrons The 5f electrons, will therefore,
be more effectively shielded from the nuclear charge than the 4f electrons
of the corresponding lanthanoids Because the outer electrons are less
firmly held, they are available for bonding in the actinoids A comparison of the actinoids with the lanthanoids, with respect to
different characteristics as discussed above, reveals that behaviour similar
to that of the lanthanoids is not evident until the second half of the
actinoid series |
1 | 4349-4352 | The 5f electrons, will therefore,
be more effectively shielded from the nuclear charge than the 4f electrons
of the corresponding lanthanoids Because the outer electrons are less
firmly held, they are available for bonding in the actinoids A comparison of the actinoids with the lanthanoids, with respect to
different characteristics as discussed above, reveals that behaviour similar
to that of the lanthanoids is not evident until the second half of the
actinoid series However, even the early actinoids resemble the lanthanoids
in showing close similarities with each other and in gradual variation in
properties which do not entail change in oxidation state |
1 | 4350-4353 | Because the outer electrons are less
firmly held, they are available for bonding in the actinoids A comparison of the actinoids with the lanthanoids, with respect to
different characteristics as discussed above, reveals that behaviour similar
to that of the lanthanoids is not evident until the second half of the
actinoid series However, even the early actinoids resemble the lanthanoids
in showing close similarities with each other and in gradual variation in
properties which do not entail change in oxidation state The lanthanoid
and actinoid contractions, have extended effects on the sizes, and
therefore, the properties of the elements succeeding them in their
respective periods |
1 | 4351-4354 | A comparison of the actinoids with the lanthanoids, with respect to
different characteristics as discussed above, reveals that behaviour similar
to that of the lanthanoids is not evident until the second half of the
actinoid series However, even the early actinoids resemble the lanthanoids
in showing close similarities with each other and in gradual variation in
properties which do not entail change in oxidation state The lanthanoid
and actinoid contractions, have extended effects on the sizes, and
therefore, the properties of the elements succeeding them in their
respective periods The lanthanoid contraction is more important because
the chemistry of elements succeeding the actinoids are much less known
at the present time |
1 | 4352-4355 | However, even the early actinoids resemble the lanthanoids
in showing close similarities with each other and in gradual variation in
properties which do not entail change in oxidation state The lanthanoid
and actinoid contractions, have extended effects on the sizes, and
therefore, the properties of the elements succeeding them in their
respective periods The lanthanoid contraction is more important because
the chemistry of elements succeeding the actinoids are much less known
at the present time 4 |
1 | 4353-4356 | The lanthanoid
and actinoid contractions, have extended effects on the sizes, and
therefore, the properties of the elements succeeding them in their
respective periods The lanthanoid contraction is more important because
the chemistry of elements succeeding the actinoids are much less known
at the present time 4 7
4 |
1 | 4354-4357 | The lanthanoid contraction is more important because
the chemistry of elements succeeding the actinoids are much less known
at the present time 4 7
4 7
4 |
1 | 4355-4358 | 4 7
4 7
4 7
4 |
1 | 4356-4359 | 7
4 7
4 7
4 7
4 |
1 | 4357-4360 | 7
4 7
4 7
4 7 Some
Some
Some
Some
Some
Applications
Applications
Applications
Applications
Applications
of d- and
of d- and
of d- and
of d- and
of d- and
f-Block
f-Block
f-Block
f-Block
f-Block
Elements
Elements
Elements
Elements
Elements
Iron and steels are the most important construction materials |
1 | 4358-4361 | 7
4 7
4 7 Some
Some
Some
Some
Some
Applications
Applications
Applications
Applications
Applications
of d- and
of d- and
of d- and
of d- and
of d- and
f-Block
f-Block
f-Block
f-Block
f-Block
Elements
Elements
Elements
Elements
Elements
Iron and steels are the most important construction materials Their
production is based on the reduction of iron oxides, the removal of
impurities and the addition of carbon and alloying metals such as Cr, Mn
and Ni |
1 | 4359-4362 | 7
4 7 Some
Some
Some
Some
Some
Applications
Applications
Applications
Applications
Applications
of d- and
of d- and
of d- and
of d- and
of d- and
f-Block
f-Block
f-Block
f-Block
f-Block
Elements
Elements
Elements
Elements
Elements
Iron and steels are the most important construction materials Their
production is based on the reduction of iron oxides, the removal of
impurities and the addition of carbon and alloying metals such as Cr, Mn
and Ni Some compounds are manufactured for special purposes such as
TiO for the pigment industry and MnO2 for use in dry battery cells |
1 | 4360-4363 | 7 Some
Some
Some
Some
Some
Applications
Applications
Applications
Applications
Applications
of d- and
of d- and
of d- and
of d- and
of d- and
f-Block
f-Block
f-Block
f-Block
f-Block
Elements
Elements
Elements
Elements
Elements
Iron and steels are the most important construction materials Their
production is based on the reduction of iron oxides, the removal of
impurities and the addition of carbon and alloying metals such as Cr, Mn
and Ni Some compounds are manufactured for special purposes such as
TiO for the pigment industry and MnO2 for use in dry battery cells The
battery industry also requires Zn and Ni/Cd |
1 | 4361-4364 | Their
production is based on the reduction of iron oxides, the removal of
impurities and the addition of carbon and alloying metals such as Cr, Mn
and Ni Some compounds are manufactured for special purposes such as
TiO for the pigment industry and MnO2 for use in dry battery cells The
battery industry also requires Zn and Ni/Cd The elements of Group 11
are still worthy of being called the coinage metals, although Ag and Au
Name a member of the lanthanoid series which is well known
to exhibit +4 oxidation state |
1 | 4362-4365 | Some compounds are manufactured for special purposes such as
TiO for the pigment industry and MnO2 for use in dry battery cells The
battery industry also requires Zn and Ni/Cd The elements of Group 11
are still worthy of being called the coinage metals, although Ag and Au
Name a member of the lanthanoid series which is well known
to exhibit +4 oxidation state Cerium (Z = 58)
Example 4 |
1 | 4363-4366 | The
battery industry also requires Zn and Ni/Cd The elements of Group 11
are still worthy of being called the coinage metals, although Ag and Au
Name a member of the lanthanoid series which is well known
to exhibit +4 oxidation state Cerium (Z = 58)
Example 4 10
Example 4 |
1 | 4364-4367 | The elements of Group 11
are still worthy of being called the coinage metals, although Ag and Au
Name a member of the lanthanoid series which is well known
to exhibit +4 oxidation state Cerium (Z = 58)
Example 4 10
Example 4 10
Example 4 |
1 | 4365-4368 | Cerium (Z = 58)
Example 4 10
Example 4 10
Example 4 10
Example 4 |
1 | 4366-4369 | 10
Example 4 10
Example 4 10
Example 4 10
Example 4 |
1 | 4367-4370 | 10
Example 4 10
Example 4 10
Example 4 10
Solution
Solution
Solution
Solution
Solution
Intext Question
Intext Question
Intext Question
Intext Question
Intext Question
4 |
1 | 4368-4371 | 10
Example 4 10
Example 4 10
Solution
Solution
Solution
Solution
Solution
Intext Question
Intext Question
Intext Question
Intext Question
Intext Question
4 10
Actinoid contraction is greater from element to element than
lanthanoid contraction |
1 | 4369-4372 | 10
Example 4 10
Solution
Solution
Solution
Solution
Solution
Intext Question
Intext Question
Intext Question
Intext Question
Intext Question
4 10
Actinoid contraction is greater from element to element than
lanthanoid contraction Why |
1 | 4370-4373 | 10
Solution
Solution
Solution
Solution
Solution
Intext Question
Intext Question
Intext Question
Intext Question
Intext Question
4 10
Actinoid contraction is greater from element to element than
lanthanoid contraction Why Rationalised 2023-24
114
Chemistry
are restricted to collection items and the contemporary UK ‘copper’ coins
are copper-coated steel |
1 | 4371-4374 | 10
Actinoid contraction is greater from element to element than
lanthanoid contraction Why Rationalised 2023-24
114
Chemistry
are restricted to collection items and the contemporary UK ‘copper’ coins
are copper-coated steel The ‘silver’ UK coins are a Cu/Ni alloy |
1 | 4372-4375 | Why Rationalised 2023-24
114
Chemistry
are restricted to collection items and the contemporary UK ‘copper’ coins
are copper-coated steel The ‘silver’ UK coins are a Cu/Ni alloy Many of
the metals and/or their compounds are essential catalysts in the chemical
industry |
1 | 4373-4376 | Rationalised 2023-24
114
Chemistry
are restricted to collection items and the contemporary UK ‘copper’ coins
are copper-coated steel The ‘silver’ UK coins are a Cu/Ni alloy Many of
the metals and/or their compounds are essential catalysts in the chemical
industry V2O5 catalyses the oxidation of SO2 in the manufacture of
sulphuric acid |
1 | 4374-4377 | The ‘silver’ UK coins are a Cu/Ni alloy Many of
the metals and/or their compounds are essential catalysts in the chemical
industry V2O5 catalyses the oxidation of SO2 in the manufacture of
sulphuric acid TiCl4 with A1(CH3)3 forms the basis of the Ziegler catalysts
used to manufacture polyethylene (polythene) |
1 | 4375-4378 | Many of
the metals and/or their compounds are essential catalysts in the chemical
industry V2O5 catalyses the oxidation of SO2 in the manufacture of
sulphuric acid TiCl4 with A1(CH3)3 forms the basis of the Ziegler catalysts
used to manufacture polyethylene (polythene) Iron catalysts are used in
the Haber process for the production of ammonia from N2/H2 mixtures |
1 | 4376-4379 | V2O5 catalyses the oxidation of SO2 in the manufacture of
sulphuric acid TiCl4 with A1(CH3)3 forms the basis of the Ziegler catalysts
used to manufacture polyethylene (polythene) Iron catalysts are used in
the Haber process for the production of ammonia from N2/H2 mixtures Nickel catalysts enable the hydrogenation of fats to proceed |
1 | 4377-4380 | TiCl4 with A1(CH3)3 forms the basis of the Ziegler catalysts
used to manufacture polyethylene (polythene) Iron catalysts are used in
the Haber process for the production of ammonia from N2/H2 mixtures Nickel catalysts enable the hydrogenation of fats to proceed In the Wacker
process the oxidation of ethyne to ethanal is catalysed by PdCl2 |
1 | 4378-4381 | Iron catalysts are used in
the Haber process for the production of ammonia from N2/H2 mixtures Nickel catalysts enable the hydrogenation of fats to proceed In the Wacker
process the oxidation of ethyne to ethanal is catalysed by PdCl2 Nickel
complexes are useful in the polymerisation of alkynes and other organic
compounds such as benzene |
1 | 4379-4382 | Nickel catalysts enable the hydrogenation of fats to proceed In the Wacker
process the oxidation of ethyne to ethanal is catalysed by PdCl2 Nickel
complexes are useful in the polymerisation of alkynes and other organic
compounds such as benzene The photographic industry relies on the
special light-sensitive properties of AgBr |
1 | 4380-4383 | In the Wacker
process the oxidation of ethyne to ethanal is catalysed by PdCl2 Nickel
complexes are useful in the polymerisation of alkynes and other organic
compounds such as benzene The photographic industry relies on the
special light-sensitive properties of AgBr The d-block consisting of Groups 3-12 occupies the large middle section of the periodic
table |
1 | 4381-4384 | Nickel
complexes are useful in the polymerisation of alkynes and other organic
compounds such as benzene The photographic industry relies on the
special light-sensitive properties of AgBr The d-block consisting of Groups 3-12 occupies the large middle section of the periodic
table In these elements the inner d orbitals are progressively filled |
1 | 4382-4385 | The photographic industry relies on the
special light-sensitive properties of AgBr The d-block consisting of Groups 3-12 occupies the large middle section of the periodic
table In these elements the inner d orbitals are progressively filled The f-block is placed
outside at the bottom of the periodic table and in the elements of this block, 4f and
5f orbitals are progressively filled |
1 | 4383-4386 | The d-block consisting of Groups 3-12 occupies the large middle section of the periodic
table In these elements the inner d orbitals are progressively filled The f-block is placed
outside at the bottom of the periodic table and in the elements of this block, 4f and
5f orbitals are progressively filled Corresponding to the filling of 3d, 4d and 5d orbitals, three series of transition
elements are well recognised |
1 | 4384-4387 | In these elements the inner d orbitals are progressively filled The f-block is placed
outside at the bottom of the periodic table and in the elements of this block, 4f and
5f orbitals are progressively filled Corresponding to the filling of 3d, 4d and 5d orbitals, three series of transition
elements are well recognised All the transition elements exhibit typical metallic properties
such as –high tensile strength, ductility, malleability, thermal and electrical conductivity
and metallic character |
1 | 4385-4388 | The f-block is placed
outside at the bottom of the periodic table and in the elements of this block, 4f and
5f orbitals are progressively filled Corresponding to the filling of 3d, 4d and 5d orbitals, three series of transition
elements are well recognised All the transition elements exhibit typical metallic properties
such as –high tensile strength, ductility, malleability, thermal and electrical conductivity
and metallic character Their melting and boiling points are high which are attributed
to the involvement of (n –1) d electrons resulting into strong interatomic bonding |
1 | 4386-4389 | Corresponding to the filling of 3d, 4d and 5d orbitals, three series of transition
elements are well recognised All the transition elements exhibit typical metallic properties
such as –high tensile strength, ductility, malleability, thermal and electrical conductivity
and metallic character Their melting and boiling points are high which are attributed
to the involvement of (n –1) d electrons resulting into strong interatomic bonding In
many of these properties, the maxima occur at about the middle of each series which
indicates that one unpaired electron per d orbital is particularly a favourable configuration
for strong interatomic interaction |
1 | 4387-4390 | All the transition elements exhibit typical metallic properties
such as –high tensile strength, ductility, malleability, thermal and electrical conductivity
and metallic character Their melting and boiling points are high which are attributed
to the involvement of (n –1) d electrons resulting into strong interatomic bonding In
many of these properties, the maxima occur at about the middle of each series which
indicates that one unpaired electron per d orbital is particularly a favourable configuration
for strong interatomic interaction Successive ionisation enthalpies do not increase as steeply as in the main group
elements with increasing atomic number |
1 | 4388-4391 | Their melting and boiling points are high which are attributed
to the involvement of (n –1) d electrons resulting into strong interatomic bonding In
many of these properties, the maxima occur at about the middle of each series which
indicates that one unpaired electron per d orbital is particularly a favourable configuration
for strong interatomic interaction Successive ionisation enthalpies do not increase as steeply as in the main group
elements with increasing atomic number Hence, the loss of variable number of electrons
from (n –1) d orbitals is not energetically unfavourable |
1 | 4389-4392 | In
many of these properties, the maxima occur at about the middle of each series which
indicates that one unpaired electron per d orbital is particularly a favourable configuration
for strong interatomic interaction Successive ionisation enthalpies do not increase as steeply as in the main group
elements with increasing atomic number Hence, the loss of variable number of electrons
from (n –1) d orbitals is not energetically unfavourable The involvement of (n–1) d electrons
in the behaviour of transition elements impart certain distinct characteristics to these
elements |
1 | 4390-4393 | Successive ionisation enthalpies do not increase as steeply as in the main group
elements with increasing atomic number Hence, the loss of variable number of electrons
from (n –1) d orbitals is not energetically unfavourable The involvement of (n–1) d electrons
in the behaviour of transition elements impart certain distinct characteristics to these
elements Thus, in addition to variable oxidation states, they exhibit paramagnetic
behaviour, catalytic properties and tendency for the formation of coloured ions, interstitial
compounds and complexes |
1 | 4391-4394 | Hence, the loss of variable number of electrons
from (n –1) d orbitals is not energetically unfavourable The involvement of (n–1) d electrons
in the behaviour of transition elements impart certain distinct characteristics to these
elements Thus, in addition to variable oxidation states, they exhibit paramagnetic
behaviour, catalytic properties and tendency for the formation of coloured ions, interstitial
compounds and complexes The transition elements vary widely in their chemical behaviour |
1 | 4392-4395 | The involvement of (n–1) d electrons
in the behaviour of transition elements impart certain distinct characteristics to these
elements Thus, in addition to variable oxidation states, they exhibit paramagnetic
behaviour, catalytic properties and tendency for the formation of coloured ions, interstitial
compounds and complexes The transition elements vary widely in their chemical behaviour Many of them are
sufficiently electropositive to dissolve in mineral acids, although a few are ‘noble’ |
1 | 4393-4396 | Thus, in addition to variable oxidation states, they exhibit paramagnetic
behaviour, catalytic properties and tendency for the formation of coloured ions, interstitial
compounds and complexes The transition elements vary widely in their chemical behaviour Many of them are
sufficiently electropositive to dissolve in mineral acids, although a few are ‘noble’ Of the
first series, with the exception of copper, all the metals are relatively reactive |
1 | 4394-4397 | The transition elements vary widely in their chemical behaviour Many of them are
sufficiently electropositive to dissolve in mineral acids, although a few are ‘noble’ Of the
first series, with the exception of copper, all the metals are relatively reactive The transition metals react with a number of non-metals like oxygen, nitrogen,
sulphur and halogens to form binary compounds |
1 | 4395-4398 | Many of them are
sufficiently electropositive to dissolve in mineral acids, although a few are ‘noble’ Of the
first series, with the exception of copper, all the metals are relatively reactive The transition metals react with a number of non-metals like oxygen, nitrogen,
sulphur and halogens to form binary compounds The first series transition metal oxides
are generally formed from the reaction of metals with oxygen at high temperatures |
1 | 4396-4399 | Of the
first series, with the exception of copper, all the metals are relatively reactive The transition metals react with a number of non-metals like oxygen, nitrogen,
sulphur and halogens to form binary compounds The first series transition metal oxides
are generally formed from the reaction of metals with oxygen at high temperatures These
oxides dissolve in acids and bases to form oxometallic salts |
1 | 4397-4400 | The transition metals react with a number of non-metals like oxygen, nitrogen,
sulphur and halogens to form binary compounds The first series transition metal oxides
are generally formed from the reaction of metals with oxygen at high temperatures These
oxides dissolve in acids and bases to form oxometallic salts Potassium dichromate and
potassium permanganate are common examples |
1 | 4398-4401 | The first series transition metal oxides
are generally formed from the reaction of metals with oxygen at high temperatures These
oxides dissolve in acids and bases to form oxometallic salts Potassium dichromate and
potassium permanganate are common examples Potassium dichromate is prepared from
the chromite ore by fusion with alkali in presence of air and acidifying the extract |
1 | 4399-4402 | These
oxides dissolve in acids and bases to form oxometallic salts Potassium dichromate and
potassium permanganate are common examples Potassium dichromate is prepared from
the chromite ore by fusion with alkali in presence of air and acidifying the extract Pyrolusite ore (MnO2) is used for the preparation of potassium permanganate |
1 | 4400-4403 | Potassium dichromate and
potassium permanganate are common examples Potassium dichromate is prepared from
the chromite ore by fusion with alkali in presence of air and acidifying the extract Pyrolusite ore (MnO2) is used for the preparation of potassium permanganate Both the
dichromate and the permanganate ions are strong oxidising agents |
1 | 4401-4404 | Potassium dichromate is prepared from
the chromite ore by fusion with alkali in presence of air and acidifying the extract Pyrolusite ore (MnO2) is used for the preparation of potassium permanganate Both the
dichromate and the permanganate ions are strong oxidising agents The two series of inner transition elements, lanthanoids and actinoids constitute
the f-block of the periodic table |
1 | 4402-4405 | Pyrolusite ore (MnO2) is used for the preparation of potassium permanganate Both the
dichromate and the permanganate ions are strong oxidising agents The two series of inner transition elements, lanthanoids and actinoids constitute
the f-block of the periodic table With the successive filling of the inner orbitals, 4f, there
is a gradual decrease in the atomic and ionic sizes of these metals along the series
(lanthanoid contraction) |
1 | 4403-4406 | Both the
dichromate and the permanganate ions are strong oxidising agents The two series of inner transition elements, lanthanoids and actinoids constitute
the f-block of the periodic table With the successive filling of the inner orbitals, 4f, there
is a gradual decrease in the atomic and ionic sizes of these metals along the series
(lanthanoid contraction) This has far reaching consequences in the chemistry of the
elements succeeding them |
1 | 4404-4407 | The two series of inner transition elements, lanthanoids and actinoids constitute
the f-block of the periodic table With the successive filling of the inner orbitals, 4f, there
is a gradual decrease in the atomic and ionic sizes of these metals along the series
(lanthanoid contraction) This has far reaching consequences in the chemistry of the
elements succeeding them Lanthanum and all the lanthanoids are rather soft white
metals |
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