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The element which exists in liquid state for a wide range of temperature and can be used for measuring high temperature is
(c) The melting point of gallium is \(30^{\circ} \mathrm{C}\) and boiling point is \(2240^{\circ} \mathrm{C}\). Thus, the element exists in liquid state for a wide range of temperature.
Which of the following is a Lewis acid?
(a) \(\mathrm{AlCl}_3\) is electron-deficient and hence acts as a Lewis acid.
The geometry of a complex species can be understood from the knowledge of type of hybridisation of orbitals of central atom. The hybridisation of orbitals of central atom in \(\left[\mathrm{Be}(\mathrm{OH})_4\right]^{-}\)and the geometry of the complex are respectively
(a) Boron has die electronic configuration:
\(
1 s^2 2 s^2 2 p_x^1 2 p_y^0 2 p_z^0
\)
In the excited state, 2 s -orbital electrons are impaired and one electron is shifted to a p-orbital. Now, hybridisation occurs between one \(s\)-and three p -orbitals to give \(s {p}^3\) hybridisation and tetrahedral geometry.
\(
1 s^2 \underbrace{2 s^1 2 p_x^1 2 p_y^1 2 p_z^0}_{\text {sp }{ }^3 \text {-hybridisation }}
\)
Which of the following oxides is acidic in nature?
(a) \(\mathrm{B}_2 \mathrm{O}_3\) is acidic in nature. It reacts with basic oxides to form metal borates. Acidic nature decreases on moving down the group.
\(
\underbrace{\mathrm{B}_2 \mathrm{O}_3}_{\begin{array}{c}
\text { More acicic } \\
\text { less basic }
\end{array}}, \underbrace{\mathrm{Al}_2 \mathrm{O}_3 \text { and } \mathrm{Ga}_2 \mathrm{O}_3}_{\text {Amphoteric }}, \underbrace{\mathrm{In}_2 \mathrm{O}_3 \text { and } \mathrm{Tl}_2 \mathrm{O}_3}_{\text {Basic }}
\)
The exhibition of highest co-ordination number depends on the availability of vacant orbitals in the central atom. Which of the following elements is not likely to act as central atom in \(\mathrm{MF}_6^{3-}\) ?
(a) The lowest atomic number among the given is boron. Boron has atomic number 5 and do not have vacant \(d\)-orbital. The element \(M\) in the complex ion \(M F_6^{3-}\) has a coordination number of six. Boron can show maximum coordination number of 4 . Thus, B can not form complex of the type \(M F_6^{3-}\).
Catenation i.e., linking of similar atoms depends on size and electronic configuration of atoms. The tendency of catenation in Group 14 elements follows the order:
(b) The tendency to form long open or closed atom chains by combination of some atoms in themselves is known as catenation. The catenation is maximum in carbon and decreases down the group.
\(
\mathrm{C} \gg \mathrm{Si}>\mathrm{Ge} \approx \mathrm{Sn}>\mathrm{Pb}
\)
This is due to high bond energy of \(\mathrm{C}-\mathrm{C}\) bonds. Down the group, size increases and electronegativity decreases, thereby, tendency to show catenation decreases.
Ionisation enthalpy \(\left(\Delta_i \mathrm{H}_1 \mathrm{~kJ} \mathrm{~mol}^{-1}\right)\) for the elements of Group 13 follows the order.
(d) On moving down the group from B to Tl , a regular decreasing trend in the ionisation energy values is not observed.
\(
\begin{array}{cccccc}
\mathrm{B} & \mathrm{Al} & \mathrm{Ga} & \mathrm{In} & \mathrm{Tl} \\
801 & 577 & 579 & 558 & 589 & \mathrm{~kJ} \mathrm{~mol}^{-1}
\end{array}
\)
In Ga , there are ten d-electrons in the penultimate shell which screen the nuclear charge less effectively and thus, outer electron is held firmly. As a result, the ionisation energy of both Al and Ga is nearly the same. The increase in ionisation energy from In to Tl is due to poor screening effect of 14 4-f electrons present in the inner shell ( order of shielding effect \(s>p>d>f\) ) and so effective nuclear charge increases, consequently ionisation enthalpies increase.
Quartz is extensively used as a piezoelectric material, it contains ____.
(b) Quartz, cristobalite and tridymite are some of the crystalline forms of silica and they are interconvertable at suitable temperature. Quartz is extensively used as a piezoelectric material.
The most commonly used reducing agent is
(d) Reducing agents are those substances which reduces other substances and it self oxidises.
\(+4\) oxidation state of \(\mathrm{Sn}\) is more stable than +2 oxidation state. Therefore, \(\mathrm{Sn}^{2+}\) can be easily oxidised to \(\mathrm{Sn}^{4+}\) and hence \(\mathrm{SnCl}_2\) acts a reducing agent.
\(
\mathrm{SnCl}_2+2 \mathrm{Cl} \rightarrow \mathrm{SnCl}_4+2 \mathrm{e}^{-}
\)
Dry ice is
(c) Carbon dioxide can be obtained as a solid in the form of dry ice allowing the liquified \(\mathrm{CO}_2\) to expand rapidly.
Note Dry ice is also called cardice. It is obtained when \(\mathrm{CO}_2\) is cooled under pressure (50-60 atm). Dry ice is used for making cold baths in the laboratory by mixing it with volatile organic solvents. It is also used as a coolant for preserving perishable articles in food industry, curing local burns and in hospitals for surgical operation of sores.
The reason for small radius of Ga compared to Al is ____.
(a, b) The additional 10 d-electrons offer poor screening effect for the outer electrons from the increased nuclear charge in Gallium. Hence, atomic radius of Gallium is less than that of aluminium.
The linear shape of \(\mathrm{CO}_2\) is due to _____.
(b, c) The linear shape of \(\mathrm{CO}_2\) is due to \(p \pi-p \pi\) bonding between carbon and oxygen and sp hybridisation of carbon.
Identify the correct resonance structures of carbon dioxide from the ones given below:
(b, d)
\(
\text { The answer is the option (ii) } \mathrm{O}=\mathrm{C}=\mathrm{O} \text { and (iv) }{ }^{-} \mathrm{O}-\mathrm{C} \equiv \mathrm{O}^{+}
\)
Match the species given in Column I with the properties mentioned in Column II.
\(
\begin{array}{|l|l|}
\hline \text { Column I } & \text { Column II } \\
\hline \text { (i) } \mathrm{BF}_4^{-} & \text {(a) Oxidation state of central atom is }+4 \\
\hline \text { (ii) } \mathrm{A1Cl}_3 & \text { (b) Strong oxidising agent } \\
\hline \text { (iii) } \mathrm{SnO} & \text { (c) Lewis acid } \\
\hline \text { (iv) } \mathrm{PbO}_2 & \text { (d) Can be further oxidised } \\
\hline & \text { (e) Tetrahedral shape } \\
\hline
\end{array}
\)
(a) (i) \(\rightarrow\) (e) (ii) \(\rightarrow\) (c) (iii) \(\rightarrow\) (d) (iv) \(\rightarrow\) (a), (b)
(i) \(\mathrm{BF}_4^{-}\): Tetrahedral shape, \(\mathrm{sp}^3\) hybridisation, regular geometry.
(ii) \(\mathrm{AlCl}_3\) : Octet of Al not complete, acts as Lewis acid.
(iii) \(\mathrm{SnO}: \mathrm{Sn}^{2+}\) can show +4 oxidation state.
(iv) \(\mathrm{PbO}_2\) : Oxidation.state of Pb in \(\mathrm{PbO}_2\) is +4 . Due to inert pair effect, \(\mathrm{Pb}^{4+}\) is less stable than \(\mathrm{Pb}^{2+}\) and hence acts as strong oxidising agent.
Match the species given in Column I with properties given in Column II.
\(
\begin{array}{|l|l|}
\hline \text { Column I} & \text { Column II } \\
\hline \text { (i) Diborane } & \text { (a) Used as a flux for soldering metals } \\
\hline \text { (ii) Gallium } & \text { (b) Crystalline form of silica } \\
\hline \text { (iii) Borax } & \text { (c) Banana bonds } \\
\hline \text { (iv) Aluminosilicate } & \begin{array}{l}
\text { (d) Low melting, high boiling, useful for measuring high } \\
\text { temperatures }
\end{array} \\
\hline \text { (v) Quartz } & \text { (e) Used as catalyst in petrochemical industries } \\
\hline
\end{array}
\)
(b) (i) \(\rightarrow\) (c) (ii) \(\rightarrow\) (d) (iii) \(\rightarrow\) (a) (iv) \(\rightarrow\) (e) (v) \(\rightarrow\) (b)
– \(\mathrm{BH}_3\) is unstable, forms diborane \(\mathrm{B}_2 \mathrm{H}_6\) by 3 centre -2 electron bonds, shows banana bonds.
– Gallium with low melting point and high boiling point makes it useful to measure high temperatures.
– Borax is used as a flux for soldering metals.
– Aluminosilicate is used as catalyst in petrochemical industries.
– Quartz, is a crystalline form of silica.
Match the species given in Column I with the hybridisation given in Column II.
\(
\begin{array}{|l|l|}
\hline \text { Column I } & \text { Column II } \\
\hline \text { (i) Boron in }\left[\mathrm{B}(\mathrm{OH})_4\right]^\pi & \text { (a) } \mathrm{sp}^2 \\
\hline \text { (ii) Aluminium in }\left[\mathrm{A1}\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{3+} & \text { (b) } \mathrm{sp}^3 \\
\hline \text { (iii) Boron in } \mathrm{B}_2 \mathrm{H}_6 & \text { (c) } \mathrm{sp}^3 \mathrm{~d}^2 \\
\hline \text { (iv) Carbon in Buckminsterfullerene } & \\
\hline \text { (v) Silicon in } \mathrm{SiO}_4^{4-} & \\
\hline \text { (vi) Germanium in }\left[\mathrm{GeCl}_6\right]^{2-} & \\
\hline
\end{array}
\)
(c) (i) \(\rightarrow\) (b), (ii) \(\rightarrow\) (c), (iii) \(\rightarrow\) (b), (iv) \(\rightarrow\) (a), (v) \(\rightarrow\) (b), \((\mathrm{vi}) \rightarrow\) (c)
Boron in \(\left[\mathrm{B}(\mathrm{OH})_4\right]^{-}\)is \(\mathrm{sp}^3\) hybridised.
Aluminium in \(\left[\mathrm{A} 1\left(\mathrm{H}_2 \mathrm{O}\right)_6\right]^{3+}\) is \(\mathrm{sp}^3 \mathrm{~d}^2\) hybridised.
Boron in \(\mathrm{B}_2 \mathrm{H}_6\) is \(\mathrm{sp}^3\) hybridised.
Carbon in Buckminsterfullerene \(\mathrm{sp}^2\) is hybridised.
Silicon in \(\mathrm{SiO}_4{ }^{4-}\) is \(\mathrm{sp}^3\) hybridised.
Germanium in \(\left[\mathrm{GeCl}_6\right]^{2-}\) is \(\mathrm{sp}^3 \mathrm{~d}^2\) hybridised.
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