Reason-Based Questions – Inorganic Chemistry-
bond break easily due to its weak nature and readily brings about the
reactions.
apparatus.
to the low solubility of He, as compared to N2 in blood, helium is used
in diving apparatus along with a mixture of oxygen.
behaviour in its group.
anomalous behaviour of fluorine is due to
- Small size
- Highest electro
negativity - Low F – F bond dissociation energy
- Non-availability of
d-orbitals in its valence shell.
4. Fluorine exhibits only – 1
oxidation state whereas other halogens exhibit higher positive oxidation states
also.
being the most electronegative atom has the tendency to accept one electron to
acquire stable electronic configuration of the nearest noble gas. Therefore
unlike other halogens, it exhibits only – 1 oxidation state. But other halogens
being less electronegative can share their respective electron with more
electronegative elements and can show a positive oxidation state. Further,
fluorine cannot expand its valence shell due to the absence of vacant d-orbitals
but other halogens have vacant d-orbitals and can expand their octets by
exciting their electrons to nd orbitals.
chlorine is HOCl < HClO2 < HClO3 < HClO4
is because of the increase in the oxidation number of the halogen atom. It increases
from HClO to HClO4. Again, the stability of the conjugate bases of
oxoacids of chlorine increases from ClO– to ClO-4
as the dispersal of negative charge increases from ClO– to ClO–4
because of the number of oxygen atom increase from ClO– to ClO–4.
and XeF5.
atom has all the filled orbitals with paired electrons and the promotion of
one, two or three electrons from 5p filled orbitals to 5d vacant orbitals will
give rise to two, four and six half-filled orbital’s i.e., only even number of
fluorine atoms can combine with Xe.
chemical compounds.
has least ionization energy except Radon which is radioactive, in its group.
Therefore it is only able to form chemical compounds.
signals.
lights are visible from long distances even in mist and fog. This is why they
are used as warning signs.
points.
gases are monoatomic and they are held together by weak Vander Waal’s forces.
Therefore, they have low boiling points.
oxoacid, HOF.
to high electronegativity and small size of fluorine atom, it cannot behave as the central atom in higher oxoacids like HOFO, HOFO2 and HOFO3
in which the oxidation state of F would be +3, +5 and +7 respectively.
molecules of halogens absorb the light in the visible region and excite their
electron to higher energy levels while the remaining light is transmitted and
its colour is actually the colour of the transmitted light. The intensity of
colour depends upon the size of the atom.
ions but fluorine does not form F–3 ions.
of the presence of vacant d-orbital’s in iodine, it readily accepts electrons
from I– to form I–3 ions but due to the absence of
d-orbital’s in fluorine, it does not accept electrons from F– ions
to form F–3 ions.
chlorine is higher than that of fluorine.
is due to the small size of the fluorine atom. Its atomic size is comparatively
smaller than chlorine atom. Therefore it experiences strong electron
repulsions. On further addition of an electron to it, it has fewer tendencies to
accept the electron in comparison to the chlorine atom. Hence it releases less
energy during the process
(g).
of H – I (295KJ mol-1). Therefore H- F behaves as the weakest acid
because it requires a maximum amount of energy to get dissociated in the aqueous
solution. It is because of the greater atomic size of iodine than fluorine.
oxidation states diminish from sulphur to polonium.
to inert pair effect, the stability of the +6 oxidation state decreases down the
group. Thus, the +6 oxidation state is most stable in case of sulphur and least
stable in case of polonium.
whilst sulphur is S8.
of high electronegativity and small size, oxygen atoms form pπ – pπ double bond with other oxygen
atom to form O =
O molecule but sulphur does not form pπ
– pπ
multiple bonds due to its larger size and prefers to form single bonds having
S8 structure.
oxidizing as well as reducing agent but SO3 can act only as
oxidizing agent.
SO2, sulphur atom exhibits +4 oxidation state which is less stable
than the oxidation state of +6. Therefore it acts as both oxidizing and reducing
agent whereas in SO3, sulphur atom exhibits +6 oxidation state.
Being more stable, it can only behave as an oxidizing agent.
XeF6 with fluorine or XeOF2 with oxygen and fluorine.
and oxygen is the most electronegative elements and are very reactive.
Therefore they form compounds with noble gases, especially with xenon.
compounds but SH6 is not.
being the most electronegative element can easily cause the promotion of
electrons from the filled to the vacant 3d orbital’s in sulphur atom but
hydrogen being less electronegative than sulphur cannot cause the promotion of
electrons. Therefore SF6 is known but SH6 is not known.
reactive than halogens.
is due to weaker bond and lesser bond energy of X–X’ bond in interhalogens than
that of halogen (X– X).
acid than sulphuric acid.
acid is +6. Due to higher oxidation state and higher electronegativity of Cl,
ClO3 part of HClO4 pulls the electrons of O-H bond more
strongly towards itself making the O-H bond weaker than SO2 part in
H2SO4. Therefore, perchloric acid is a stronger acid than
sulphuric acid
is less than that of Cl2.
to the smaller size, the lone pairs of electron on the fluorine atom repel the bond
pair of the F- F bond but due to the bigger size of electrons, the repulsion
between bond pair and lone pair is comparatively less in chlorine atom. Hence the bond energy of F2 is less than that of Cl2.
does not.
has vacant d-orbital but F has no d-orbital. Again because of the bigger size of
chlorine, it can accommodate three F atoms but due to the smaller size of fluorine,
it cannot accommodate large-sized Cl atoms around it.
positive oxidation state like other group members? Also, report the compound
where oxygen shows a positive oxidation state.
does not positive oxidation state because it does not have vacant d – orbital.
So, there is no place to accommodate the excited electrons. Therefore, no
sharing of the electron is possible.
is the most electronegative element next to fluorine. It shows a positive oxidation
state only in compounds with fluorine, e.g., it has a positive oxidation state in
OF2.
oxidation state decreases from sulphur to polonium in group 16. Why?
elements of group 16 have the ground state valence shell electronic
configuration is ns2 np4 and tends to attain noble gas
configuration by gaining or sharing two electrons. Oxygen with its high electronegative value tends to complete its octet by gaining two electrons and
exhibits -2 oxidation state. The electronegativity of other element is very
less and hence, there is a low probability for them to form divalent negative
ions. The decreasing electronegativity value of the elements in this family
with increasing atomic number suggests that the tendency to show -2 oxidation
state decreases from sulphur onward to polonium.
not known?
configuration of oxygen is 1s2 2s2 2p2. Since
it does not have any 2d orbital’s in its valence shell, so it cannot expand its
octet due to non-availability of d orbitals. Hence, oxygen atom cannot exhibit
higher positive oxidation state, and hence, OF6 compound is not
known.
oxidizing agent. Give reasons.
in SO2 has oxidation state +4. It lies in between the minimum
oxidation state (-2) and maximum oxidation state (+6) of S. Thus, S in SO2
can show an increase in its oxidation number (i.e., can act as reductant) or
can show a decrease in its oxidation number (i.e., can act as an oxidant). On the
other hand, in H2S, S is in -2 oxidation state and can only increase
its oxidation state to act as reductant.
powerful reducing agent in an alkaline medium than in acidic medium. Why?
Ans. The
reducing property may be represented as SO2 + 2OH– → SO42- + 2e–
of acid favours the reverse reaction whereas addition of OH– favours
the forward reaction.
through a fluorine solution, no reaction takes place. Explain.
to the small size and high electronegativity, fluorine is a stronger oxidizing
agent than chlorine. Hence, chlorine cannot displace or oxidize fluorine ions
to fluorine. Chlorine shows different oxidation states in its compounds.
from KI but the same metal ion does not liberate Cl2 from KCl?
is because I– is a stronger reducing agent as compared to Cl–
and thus, KI reduces the metal ion to liberate I2. For example KI on
reaction with Cu2+ liberates I2 and Cu2+ get
reduced to Cu1+.
4KI
+ 2Cu2+ → I2
+ Cu2I2 + 4K+
oxidizing powers of fluorine and chlorine.
of low bond dissociation energy of fluorine, it is a stronger oxidizing agent.
oxoacids like other halogens?
shows only -1 oxidation state due to the highest electronegativity whereas, in
oxoacids, the element involved should have positive oxidation state. Thus,
fluorine does not form oxoacids.
metallic nature.
possesses metallic lustre, forms ionic compounds such as IPO4, I(CH3COO)3
having a +3 oxidation state.
acquires a brown colour after some time. Why?
is a strong reducing agent and on keeping, it gets slowly oxidized to brown coloured
iodine by oxygen.
4HI
+ O2 → 2I2 + 2H2O
Why?
electron affinity of halogen is maximum among all groups. Higher is the
electron affinity more is the tendency to gain an electron and thus more is the
tendency to get itself reduced and more is oxidizing power.
X +
e– → X– ∆ H = -E
(higher values)
than other halogens?
is more reactive than other halogens due to the following reasons:
dissociation energy due to repulsion between its non-bonding electrons.
Fluorine cannot form multiple
bonds because of the absence of d orbitals.
Fluorine has a small size and
high electronegativity, and due to this it has a greater tendency to accept an
electron to form a more stable fluoride ion.
The extent of hydration in F–
is maximum.
fluorine existing only the -1 and zero oxidation states whereas iodine exists
in +1, 0 and -1 oxidation states?
being the most electronegative element combines with other elements by ionic
or polar covalent bonds in which it is negatively polarized. Thus, its
oxidation state is -1. But when fluorine atoms combine with each other to form
F2 oxidation state of fluorine is zero.
character of the halogen varies as we move down the group.
to their high electron affinities, halogens act as strong oxidizing agents. But
their oxidizing power goes on decreasing on moving down the group from the
fluorine to iodine due to the increase in the size of the atoms. The decreasing
trend in oxidizing power is quite evident from their respective standard reduction
potential which is maximum for fluorine and minimum for iodine.
krypton other noble gas elements do not form compounds. Explain.
xenon has lower ionization energy as compared to other noble gas elements.
solubility of noble gases in the water?
increase in solubility of noble gases down the group is due to the increase in
polarization with the increase in sizes. The basic cause of solubility of noble
gases in water is due to dipole induced dipole attraction between water
molecules and noble gases.
form compounds with highly electronegative fluorine and oxygen?
and neon do not form compounds with highly electronegative fluorine and oxygen
because these noble gases have high ionization energy and they do not have d
orbitals in their valence shells.
of noble gases increases down the group?
of noble gases depends upon the atomic size. Vander Waal’s forces increase down
the group, and therefore, the tendency of liquefaction also increases down the
group.
larger radii in their periods.
the noble gases, we can measure only Wander Waal’s radii which are larger than
covalent radii.
aeroplane tyres and to fill the weather balloons through its lifting power is
only 90% of hydrogen?
is because hydrogen gas is highly inflammable; therefore, it may catch fire
with an explosion. On the other hand, helium gas is non-inflammable, so there is
no danger of fire or explosion.
18 known as noble gas?
elements of group 18 have their valence shell orbitals completely filled. As a
result, they are fairly non-reactive and hence are called noble gases. However,
Xe reacts with highly electronegative elements such as oxygen and fluorine
under certain conditions to form oxides, fluorides and ox fluorides.
of the transition metals are high.
metals have strong metallic bonds between the atoms of these elements.
Therefore a high amount of heat is required to break the metal lattice to give
free atoms.
generally form coloured compounds.
transition metals have in complete d-subshell or have unpaired electrons in
their d-subshell due to which d-d transition takes place and they become
coloured.
of their compounds show paramagnetic behaviour.
transition metals have unpaired electrons in (n – 1) d-orbital. Therefore
their ions and compounds are paramagnetic.
stable in aqueous solution.
Ans. Cu+2
is much more stable than Cu+ (aq). It is because although second
ionization enthalpy of copper is large but enthalpy of hydration (Δhy H)
for Cu+ (aq) is much more negative than that for Cu+2
(aq) and hence it more than compensates for the second ionization enthalpy of
copper and they readily undergo disproportionately in aqueous solution. 2Cu+ → Cu+2 + Cu
greater from element to element than Lanthanoid concentration.
is due to poor shielding by 5f electrons in the actinoids than that by 4f
electrons in the lanthanoids.
metal is basic, the highest is acidic.
the low oxidation state of the metal, some of the valence electrons of the
metal atom are not involved in bonding. Hence it can donate electrons and
behave as a base but in higher oxidation state, valence electrons are involved in
bonding and are not available. Therefore it can accept electrons and hence
behave as acid.
transition metal.
copper in the oxidation state of +2, it has electronic configuration of 4so3d9,
i.e., incompletely filled d-subshell.
ions yet it is regarded as a transition element.
in the ground, the state has one electron in the 3d-subshell. Therefore it is
regarded as transition element but in +3 oxidation state, it has no electron in
3d subshell (3do). Hence it does not form coloured ions.
enthalpies of hydration.
of transition, elements have a small atomic size and high nuclear charge. Both the
properties change as we move from left to right along the transition series.
variable oxidation states.
the transition elements, the energies of (n – 1) d orbitals and ns orbitals are
very close or there is little difference in them. Hence electrons from both can
take part in bonding.
irregularities in their electronic configuration.
to the very small difference in the energy of (n – 1)d-subshell and ns subshell,
the incoming electron may enter into ns or (n – 1) d subshell. Therefore, they
show irregularities in their electronic configuration.
3d transition series elements increase up to Mn and then decreases.
moving from Sc to Mn, the numbers of unpaired electrons increases and hence
paramagnetic character increases. But after Mn, the pairing of electrons in the
d-subshell starts and the number of unpaired electrons decreases and hence
paramagnetic character decreases.
white, white Cu+2 salts are blue.
has completely filled d-orbital’s (3d10) causing no d-d transition
but due to the presence of unpaired electrons or incompletely filled d-orbital’s
(3d9) the d-d transition takes place and Cu+2 salts are blue.
of Zn, Cd and Hg are low.
Zn, Cd and Hg have completely filled d-subshell i.e. all the electrons in
d-subshell are paired. Hence the metallic bonds present in them are weak.
Therefore they have low melting and boiling points.
is difficult.
to lanthanide contraction, the change in the atomic or ionic radii of these
elements is very small. Hence their chemical properties are similar which makes
their separation difficult.
lanthanoids is not known with certainty.
the lanthanoids, 4f and 5d subshell are very close in energy. The outer most 6s
orbital remains filled with 2 electrons (6s2). The electron can
easily jump from 4f to 5d or vice-versa. Therefore their electronic configuration
is not known with certainty.
and third transition series elements show a similar size.
to lanthanide concentration, the size of an atom of the third transition
series is almost the same as that of the element present just above in the
second transition series. Hence there is similarity in their properties.
same atomic radii.
Mn and Fe have nearly the same effective nuclear charge. Hence they have almost the same atomic radii.
white.
salts are white because it has completely filled d-orbitals (d10) and
there is no possibility of d-d transition.
covalency between manganese and oxygen.
permanganate ion (MnO–4) ion, manganese is in its highest
oxidation state i.e. + 7 and in its high oxidation state, transition metals
form covalent bonds.
more stable than Fe+2 towards oxidation to their +3 state.
configuration of Mn+2 shows that it has half-filled (3d5)
sub-shell, exhibiting extra stability. Therefore third ionization enthalpy is
very high and it cannot lose the third electron easily. In the case of Fe+2, an electronic configuration is 3d6 and it can lose the third electron
easily to give stable configuration 3d5.
extraction of silver from its ore.
cyanide on reaction with the ore of silver forms sodium Argento cyanide. It is
a soluble complex from which the silver can be precipitated easily by adding
more electropositive metal like zinc to it.
Lu(OH)3, the former one is more basic
the size of the lanthanoid decreases from La+3 to Lu+3
the covalent character of the hydroxides increases. Hence the basic strength
decreases from La(OH)3 to Lu(OH)3.
but Mn+3 is oxidizing when both have d4 configuration.
have d4 configuration and easily changes to Cr+3 because
d3 has half-filled t2g orbital and hence more stable.
Therefore it is reducing. On the other hand, Mn+2 is more stable due
to half-filled d5 configuration and Mn+3 can easily be
changed to Mn+2 and therefore it is oxidizing.
reducing agent than H2O.
H-S bond is weaker than H-O because of the lesser tendency of S for overlapping due
to lower electronegativity and larger size of the anion S2-. Thus,
H2S having weaker bond acts as a better reducing agent.
oxygen is a gas at room temperature.
forms a stable diatomic molecule. In oxygen molecules, two atoms of oxygen have
joined together through a double bond (pπ
– pπ bonding) as O=O. The multiple bonding in oxygen
is possible due to the small size of oxygen atoms. Thus, oxygen is a gas and no
more atoms of oxygen can join.
molecules like oxygen or chlorine?
no unpaired electron is present in its electronic configuration (1s2
2s2 2p6 3s2 3p6) and it has very
high ionization energy.
is less than the bond dissociation energy of chlorine.
is due to strong inter-electronic repulsion between nonbonding electrons in small
size 2p orbitals of fluorine as compared to big sizes 3p orbitals of chlorine
and this makes the bond dissociation energy of F2 less than that of
Cl2.
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