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Chemistry Test - 34
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  • Question 1
    1 / -0

    Match the hybrid bond orbitals  of list I with the species of the list II and pick out the correct ?

          List I                            List II

    (A) sp3                          1. [Ni(CN)4]2

    (B) dsp2                        2. Ni(CO)4

    (C) sp3d                        3. BrF-4

    (D) sp3d2                       4. ClF3

    Solution
    \(\mathrm{Ni}(\mathrm{CO})_{4}-\mathrm{sp}^{3}\)
    \(\left[\mathrm{Ni}(\mathrm{CN})_{4}\right]^{2-}-\mathrm{d} \mathrm{sp}^{2}\)
    \(B r F_{4}^{-}-s p^{3} d^{2} \quad(4 \mathrm{bp}+2 \mathrm{lp})\)
    \(C l F_{3}-s p^{3} d \quad(3 \mathrm{b} \mathrm{p}+2 \mathrm{lp})\)
    HENCE OPTION 4 IS THE CORRECT ANSWER.
    Hence, the correct option is (D)
  • Question 2
    1 / -0

    Which of the above compounds are enantiomers?

    Solution

    (i),(ii),(iv) have plane of symmetry, so they'll be meso compound. So its mirror image is identical.

    Non-Mirror image to each other so III and V are enantiomers.
    Hence, the correct option is (C)

  • Question 3
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    Give the IUPAC name of :

    Solution

    There are two skills you have to develop in this area:
    You need to be able to translate the name of an organic compound into its structural formula.
    You need to be able to name a compound from its given formula.

    The first of these is more important (and also easier!) than the second. In an exam, if you can't write a formula for a given compound, you aren't going to know what the examiner is talking about and could lose lots of marks. However, you might only be asked to write a name for a given formula once in a whole exam - in which case you only risk 1 mark.

    So, we're going to look mainly at how you decode names and turn them into formulae. In the process you will also pick up tips about how to produce names yourself.

    In the early stages of an organic chemistry course people frequently get confused and daunted by the names because they try to do too much at once. Don't try to read all these pages in one go. Just go as far as the compounds you are interested in at the moment and ignore the rest. Come back to them as they arise during the natural flow of your course.

    Hence, the correct option is (C)

  • Question 4
    1 / -0

    First and second ionization energies of Magnesium are 7.646 and 15.035 eV respectively. The amount of energy in KJ needed to convert all the atoms of Magnesium into Mg2+ ions present in 12 mg of Magnesium vapours is :
    [ Given : 1 eV = 96.5 kJ mol-1 ]

    Solution

    \(\frac{12 \mathrm{mg}}{24 \mathrm{g}}=0.5 \times 10^{-3} \mathrm{moles}\)

    Energy per atom \(=7.646+15.035=22.68 \mathrm{eV}\)

    \(22.68 \times 96.48=21.88 \times 10^{2} \mathrm{KJ} / \mathrm{mole}\)

    E(needed) \(21.88 \times 10^{2} \times 0.5 \times 10^{-3}\)

    \(10.94 \times 10^{-1}=1.094 \mathrm{KJ}\)

    The ionization potential is the minimum amount of energy required to remove one electron from each atom in a mole of atoms in the gaseous state. The first ionization energy is the energy required to remove two, the ionization energy is the energy required to remove the atom's nth electron, after the (n −1) electrons before it have been removed. Trend-wise, ionization energy tends to increase while one progresses across a period because the greater number of protons (higher nuclear charge) attract the orbiting electrons more strongly, thereby increasing the energy required to remove one of the electrons. Ionization energy and ionization potentials are completely different. The potential is an intensive property and it is measured by "volt" ; whereas the energy is an extensive property expressed by "eV" or "kJ/mole".

    As one progresses down a group on the periodic table, the ionization energy will likely decrease since the valence electrons are farther away from the nucleus and experience a weaker attraction to the nucleus's positive charge. There will be an increase of ionization energy from left to right of a given period and a decrease from top to bottom. As a rule, it requires far less energy to remove an outer-shell electron than an inner-shell electron. As a result, the ionization energies for a given element will increase steadily within a given shell, and when starting on the next shell down will show a drastic jump in ionization energy. Simply put, the lower the principal quantum number, the higher the ionization energy for the electrons within that shell. The exceptions are the elements in the boron and oxygen family, which require slightly less energy than the general trend. Helium has the highest ionization energy while Francium has the lowest.

    Factor Influencing Ionization energy

    Variation in ionization energies in a period and group may or may not be regular and can be influenced by the following factor.

    (A)Size of the Atom :ionization energy decreases with increase in atomic size.

    As the distance between the outer most electrons and the nucleus increases, the force of attraction between the valence shell electrons and the nucleus decreases. As a result, outer most electrons are held less firmly and a lesser amount of energy is required to knock them out.

    For example, ionization energy decreases in a group from top to bottom with an increase in atomic size.

    (B)Magnitude of Nuclear Charge:ionization energy increases with an increase in nuclear charge. This is due to the fact that with an increase in nuclear charge, the electrons of the outer most shell are more firmly held by the nucleus and thus greater amount of energy is required to pull out an electron from the atom.

    For example, ionization energy increases as we move from left to right along a period due to the increase in nuclear charge.

    (C)Shielding or screening effect :

    The inner electronic shells act as a screen between the nucleus and the outer shell. This reduces the inward pull of the outer shell towards the nucleus. In other words, the electrons that lie between the nucleus and the valence (i.e. outermost) shell have a shielding or screening effect on the electrons of valence (i.e. outermost) shell. This is called the shielding effect. The larger the number of electrons in the inner shells, the greater will be the screening effect and lesser will be the nuclear attraction of the outermost electrons. Thus increase in the number of inner electrons will tend to decrease ionization energy. It should be carefully noted that electrons in the same or similar type of orbital do not shield each other. Thus the electrons in s-orbital will not shield each other. Similaly, electrons in px, py and pz orbital of the same subshell do not shield each other. It has also been found that the screening effect of

    s-electrons is more than that of p-electron shoes effect is in turn more than that of a d-electron and so on.

    (D)Penetration effect of the electron :

    The ionization energy also depends on the type of electron which is removed. s, p, d and f electrons have orbitals with different shapes. An s electron penetrates close to the nucleus, and is therefore more tightly held than a p electron. Similarly a p-orbital electron is more tightly held than a d-orbital electron and a d-orbital electron is more tightly held than an f-orbital electron. All other factors being equal, ionization energies are in the order s>p>d>f .

    For example, the ionization energy of aluminium is comparatively less than magnesium because the outer most electron is to be removed from a 3p-orbital (having lesser penetration effect) in aluminium where as in magnesium it will be removed from a 3s-orbital (having larger penetration effect) of the same energy level.

    (E)Electronic Configuration :

    If an atom has exactly half-filled or completely filled orbitals, then such an arrangement has extra stability.

    The removal of an electron from such an atom requires more energy then expected. For example, the first ionization energy of beryllium is greater than boron because beryllium has an extra stable completely filled outer most 2s orbital while boron has a partially filled less stable outer most 2p-orbital.

    Be \((Z=4) 1 s^{2}, 2 s^{2}\)

    \(\mathbf{B}(\mathbf{Z}=5) 1 \mathbf{s}^{2}, 2 \mathbf{s}^{2}, 2 \mathbf{p}^{1}\)
    Hence, the correct option is (A)

  • Question 5
    1 / -0

    When H2O2 is added to ice cold solution of acidified potassium dichromate in ether and the contents are shaken and allowed to stand :

    Solution

    When H2O2 is added acidified potassium dichromate in ether solution, potassium dichromate is oxidised to blue peroxide of chromium (CrO5) which is soluble in ether and produces blue coloured solution.

    K2Cr2O7 + H2SO4 + 4H2O2 2CrO5 + K2SO4 + 5H2O
    Hence, the correct option is (B)

  • Question 6
    1 / -0

    The electrochemical cell shown below is a concentration cell.
     

    \(\mathrm{M} \mid \mathrm{M}^{2}\left(\right.\) saturatedsolutionofasparinglysolublesalt,MX \(\left._{2}\right) \mathrm{M}^{2}\left(0.001 \mathrm{moldm}^{-3}\right) \mid \mathrm{M}\)
    The emf of the cell depends on the difference in concentrations of \(\mathrm{M}^{2+}\) ions at the two electrodes. The emf of the cell at \(298 \mathrm{K}\) is \(0.059 \mathrm{V}\).
    The value of \(\Delta \mathrm{G}\left(\mathrm{kJmol}^{-1}\right)\) for the given cell is \(\left(\right.\) Take \(\left.1 \mathrm{F}=96500 \mathrm{Cmol}^{-1}\right)\)
    Solution
    At anode : \(M(s) \quad+2 X^{-}(a q) \rightarrow M^{2+} X_{2}+2 e^{-}\)
    At cathode : \(M^{+2}(a q)+2 e^{-} \rightarrow M(s)\)
    n-factor of the cell reaction is 2
    \(\Delta \mathrm{G}=-\mathrm{nFE}_{\text {cell }}=-2 \times 96500 \times 0.0591=-11406.3 / \mathrm{mole}\)
    \(=-11.4 \mathrm{KJ} / \mathrm{mole}\)
    Hence, the correct option is (D)
  • Question 7
    1 / -0

    The standard e.m.f. of a cell, involving one electron change is found to be 0.591V at 25o C.The equilibrium constant of the reaction is-

    \(F=96500 \mathrm{C} \mathrm{mol}^{-1}, \mathrm{R}=8.314 \mathrm{JK}^{-1} \mathrm{mol}^{-1}\)
    Solution
    \(\Delta G=\Delta G^{\circ}-\frac{0.591}{n} \log Q\)
    at equilibirium \(\Delta G=0, \quad \mathrm{Q}=\mathrm{K}_{\mathrm{C}}, \Delta G^{\circ}=n R E\)
    \(\mathrm{E}_{\text {cell }}=\mathrm{E}_{\text {cell }}^{\mathrm{o}}-\frac{0.0591}{\mathrm{n}} \log \mathrm{K}_{\mathrm{c}}\)
    \(0=0.591-\frac{0.0591}{1} \log \mathrm{K}_{\mathrm{c}}\)
    \(\Rightarrow-0.591=-0.0591 \log \mathrm{K}_{\mathrm{c}}\)
    \(\Rightarrow \quad \log \mathrm{K}_{\mathrm{c}}=\frac{0.599}{0.0591}=10\)
    \(\therefore \quad \mathrm{K}_{\mathrm{c}}=\) antilog \(10=1 \times 10^{10}\)
    Hence, the correct option is (C)
  • Question 8
    1 / -0

    The enthalpy change of the reaction

    \(\mathrm{H}_{(a q)}^{+}+\mathrm{OH}_{(a q)}^{-} \longrightarrow \mathrm{H}_{2} \mathrm{O}_{(l)}\) is \(-57.3 \mathrm{kJ} \mathrm{mol}^{-1}\). If the enthalpies of Formation of \(\mathrm{H}_{(a q)}^{+}\) and \(\mathrm{H}_{2} \mathrm{O}_{(l)}\) are zero and
    \(-285.84 \mathrm{kJ} \mathrm{mol}^{-1}\) respectively, then the enthalpy of formation of \(\mathrm{OH}_{(a q)}^{-}\) is
    Solution
    \(\mathrm{H}^{+}(\mathrm{aq})+\mathrm{OH}^{-}(\mathrm{aq}) \rightarrow \mathrm{H}_{2} \mathrm{O} ; ; \Delta \mathrm{H}=-57 \cdot 3 \mathrm{kJ} \mathrm{mol}^{-1}\)
    \(\Delta \mathrm{H}=\Sigma \Delta \mathrm{H}_{\mathrm{f}}(\) Products \()-\Sigma \Delta \mathrm{H}_{\mathrm{f}}(\) Reactants \()\)
    \(\Delta \mathrm{H}_{\mathrm{r}}=\Delta \mathrm{H}_{\mathrm{f}}\left(\mathrm{H}_{2} \mathrm{O}\right)-\left(\Delta \mathrm{H}\left(\mathrm{H}^{+}\right)+\Delta \mathrm{H}\left(\mathrm{OH}^{-}\right)\right)\)
    \(\Delta \mathrm{H}_{\mathrm{f}}\left(\mathrm{OH}^{-}\right)=-285 \cdot 84-(-57 \cdot 3)=-228 \cdot 54 \mathrm{kJ} \mathrm{mol}^{-1}\)
    Hence, the correct option is (A)
  • Question 9
    1 / -0

    Identify the final product (Z) in the following sequence of reactions :

    \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH} \frac{1 . \mathrm{LiAH}_{4}}{2 . \mathrm{PBr}_{3}}(\mathrm{X}) \stackrel{\mathrm{KCN}}{\longrightarrow}(\mathrm{Y}) \stackrel{\mathrm{LiAlH}_{4}}{\longrightarrow}(\mathrm{Z})\)
    Solution
    \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COOH} \underset{\text { Reduction }}{\mathrm{LAlH}_{4}} \underset{\text { Benzyl alcohol }}{\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{OH}} \stackrel{\mathrm{PBr}_{3}}{\longrightarrow} \mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{Br} \stackrel{\mathrm{KCN}}{\mathrm{X}} \mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{CN}\)
    \(\frac{\text { LAIH }_{4}}{\text { Reduction }} \mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{NH}_{2}\)
    Hence, the correct option is (B)
  • Question 10
    1 / -0

    Amongst the halides

    (1)  BCl3           (2)  AlCl3

    (3)  GaCl3        (4)  InCl3

    The order of decreasing Lewis acid character is

    Solution

    Lewis acid strength of group 13 halides follow the order :BCl3 > AlCl3 > GaCl3 > InCl3.

    As we move down the group, the size of atom increases, and as a result, the tendency to attract electrons decreases. This leads to a decrease in Lewis acid nature down the group

    Chemical properties of elements boron family group (IIIA)Some properties of the boron group elements

      Boron Aluminum  
    Atomic number 5 13  
    Atomic weight 10.81 26.982  
    Colour of element Brown Silver-white  
    Meltting point (oC) 2,075 660.32  
    Boiling point (oC) 4,000 2,519  
    Decsity      
    Solid (grams per cubic centimetre at 20oC) 2.34 2.699  
    Liquid (grams per millilitre) 2.37 2.375  
    Valence 3 3  
    Mass number of most common isotopes (terrestrial abundance, percent) 10 (19.92), 11 (80.12) 27 (100)  
    Radioactive isotopes (mass numbers) 7-9, 12-19 21-26, 28-41  
    Colour imparted to flame Green Colourless  
    Colour of ions in solution      
    +3 - Colourless  
    +1 - -  
    Heat of fusion (calories per mole/kilojoules per mole) 12,000 (50) 2,560 (10.7)  
    Specific heat (joules per gram kelvin) 1.026 0.897  
    Electrical resistivity at 20-25oC (microhmcentimetres) >1012 2.7  
    Hardness (Moh's scale) 9.3 2.75  
    Crystal structure at 20oC Alpha-rhombohedral, betarhombohedral, tetragonal Face-centred cubic  
    Radius      
    Atomic (angstroms) 0.87 1.18  
    Ionic (angstroms) 0.41 0.68  
    Ionization energy (electron volts)      
    First 800.6 577.5  
    Second 2,427.10 1,816.70  
    Third 3,659.70 2,744.80  
    Fourth 25,025.80 11,577  
    Oxidation potential for oxidation from the 0 to +3 oxidation state at 25oC (volts) - 1.68  
    Electronegativity (pauling) 2.04 1.61  
      Gallium Indium Thallium
    Atomic number 31 49 81
    Atomic weight 69.723 114.818 204.383
    Colour of element Gray-blue Silver-white Blue-white
    Meltting point (oC) 26.76 156.6 304
    Boiling point (oC) 2,204 2,072 1,473
    Density      
    Solid (grams per cubic centimetre at 20oC) 5.904 7.31 11.85
    Liquid (grams per millilitre) 6.095 7.02 11.22
    Valence 3 3,1 3,1
    Mass number of most common isotopes (terrestrial abundance, percent) 69 (60.108), 71 (39.892) 113 (4.29), 115 (95.71) 203 (29.52), 205 (70.48)
    Radioactive isotopes (mass numbers) 60-68, 70, 72-86 97-112, 114-135 176-202, 204, 206-212
    Colour imparted to flame Violet Blue Green
    Colour of ions in solution      
    +3 Colourless Colourless Colourless
    +1 - - Colourless
    Heat of fusion (calories per mole/kilojoules per mole) 1,340 (5.59) 779 (3.26) 1,000 (42)
    Specific heat (joules per gram kelvin) 0.373 0.233 0.129
    Electrical resistivity at 20-25oC (microhmcentimetres) 14 8 15
    Hardness (Moh's scale) 1.5 1.2 1.2
    Crystal structure at 20oC Orthorhombic Face-centred tetragonal Hexagonal close-packed
    Radius      
    Atomic (angstroms) 1.36 1.56 1.56
    Ionic (angstroms) 0.76 0.94 1.03
    Ionization energy (electron volts)      
    First 578.8 558.3 589.4
    Second 1,979.30 1,820.70 1,971
    Third 2,963 2,704 2,878
    Fourth 6,180 5,210 -
    Oxidation potential for oxidation from the 0 to +3 oxidation state at 25oC (volrs) 0.53 0.34 -1.25
    Electronegativity (pauling) 1.81 1.78 1.62
    Density at 25oC      

    Hence, the correct option is (A)

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