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Thermodynamics Test - 32

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Thermodynamics Test - 32
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  • Question 1
    1 / -0
    A spontaneous process may be defined as :
  • Question 2
    1 / -0
    Ideal gas is contained in a thermally insulated and rigid container and it is heated through a resistance $$100\Omega $$ by passing a current of $$1A$$ for five minutes, then change in internal energy of the gas is
    Solution
    $$\Delta W=0$$
    $$\therefore \Delta Q=\Delta U$$
    $$\Delta Q=\Delta U={ I }^{ 2 }R\Delta t={ 1 }^{ 2 }(100)(5\times 60)=30kJ$$
  • Question 3
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    Directions For Questions

    The electrochemical cell shown below is a concentration cell.
    $$M | M^{2+} \left (\text {Saturated solution of sparingly soluble salt}, MX_{2}\right ) | | M^{2+}(0.001\ mol\ dm^{-3})|M$$
    The emf of the cell depends on the difference in concentrations of $$M^{2+}$$ ions at the two electrodes. The emf of the cell at $$298\ K$$ is $$0.059\ V$$.

    ...view full instructions

    The value of $$\triangle G (kJ\ mol^{-1})$$ for the given cell is: (take $$1F = 96500\ C\ mol^{-1})$$
    Solution
    $$\triangle G = -nFE$$
    $$= -2\times 96500\times 0.059$$
    $$= -11.4\ kJ/mol$$.
  • Question 4
    1 / -0
    A piece of ice kept at room temperature melts of its own. This reaction is governed by which law?
    Solution
    When ice changes into water spontaneously at room temperature, the randomness increases, so entropy increases, which is in accordance with the second law of thermodynamics.
  • Question 5
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    Which of the following pairs of a chemical reaction is certain to result in a spontaneous reaction?
    Solution
    A chemical reaction which is exothermic and has an increasing disorder is certain to result in a spontaneous reaction.
    Since the reaction is exothermic, $$ \displaystyle \Delta H $$ is negative. Since, the disorder increases, $$ \displaystyle \Delta S $$ is positve.

    $$ \displaystyle \Delta G  =\Delta H - T\Delta S = -ve  -  ( +ve \times +ve) =-ve$$

    Negative value of $$ \displaystyle \Delta G$$ corresponds to spontaneous process.
  • Question 6
    1 / -0
    Match the List-II ans List-II and List III:
    List-IList-IIList-III
    A. $$\Delta \, G>0$$X. $$\Delta \, S>0$$1. Non-spontaneous
    B. $$\Delta \, G<0$$Y. $$\Delta \, S<0$$2. Spontaneous
    C. $$\Delta \, G=0$$Z. $$\Delta \, S=0$$3. Equilibrium
    select the correct answering from the following codes:
    Solution
    According to the third law, the entropy change of a spontaneous process is always greater than zero.
    For spontaneous process $$\Longrightarrow \quad \Delta G<0\quad and\quad \Delta S>0$$
    For non-spontaneous process  $$\Longrightarrow \quad \Delta G>0\quad and\quad \Delta S<0$$
    For equilibrium process  $$\Longrightarrow \quad \Delta G=0\quad and\quad \Delta S=0$$
  • Question 7
    1 / -0
    If $$\triangle H_{vaporisation}$$ of substance $$X(l)$$ (molar mass: $$30\ g/mol)$$ is $$300\ J/g$$ at it's boiling point $$300\ K$$, then molar entropy change for reversible condensation process is____________.
    Solution
    Solution:- (A) $$30 \; {J}/{mol-K}$$
    Given:-
    $${\Delta{H}}_{vap.} = 300 \; {J}/{g}$$
    Molar mass of $$X = 30 \; {g}/{mol}$$
    $$\therefore {\Delta{H}}_{molar} = 300 \times 30 = 9000 \; {J}/{mol}$$
    Boiling point of substance $$X, \; \left( T \right) = 300 K$$
    As we know that,
    Molar entropy change, $${\Delta{S}}_{molar} = \cfrac{{\Delta{H}}_{molar}}{T} = \cfrac{9000}{300} = 30 \; {J}/{mol-K}$$
    Hence the molar entropy change for the given process will be $$30 \; {J}/{mol-K}$$.
  • Question 8
    1 / -0
    Heat of combustion $$\Delta H^o$$ for $$C(s), H_2(g)$$ and $$CH_4(g)$$ are $$-94,-68$$ and $$-213 kcal/mol$$ respectively. Then $$\Delta H^o$$  for $$C(s) + 2H_2(g) \rightarrow CH_4$$ is:
    Solution
    For reaction,
    $$C(s)+2H_2(g)\rightarrow CH_4(g), \Delta H^o=?$$

    $$\Delta H^o$$= $$- $$[($$\Delta H^o$$ of combustion of $$CH_4$$) - ($$\Delta H^o$$ of combustion of  $$C$$)+ (2 $$\times \Delta H^o $$ of combustion of $$H_2$$)]

    $$C + O_2 \rightarrow CO_2; \Delta H^o = - 94\, kcal$$ ... (i)


    $$2H_2+O_2 \rightarrow 2H_2O; \Delta H^o = - 68\times 2\, kcal$$ ... (ii)

                       $$=-[(-213)-(-94+2\times -68)]\, kcal/mol$$

                       $$=-[-213+230]=-17\,kcal/mol$$
  • Question 9
    1 / -0
     $$H_{2(g)} + \dfrac{1}{2} O_{2(g)} \rightarrow H_2O_{(g)}$$$$\Delta H = 241.8 kJ$$ $$CO_{(g)} + \dfrac{1}{2} O_{2(g)} \rightarrow CO_{2(g)}$$ $$\Delta H = 283 kJ$$ 
    The heat evolved during the combustion of $$112$$ litre of water gas (mixture of equal volume of $${H}_{2}$$ and $$CO$$) is:
    Solution
    Solution:- (C) $$1312 \; KJ$$
    Molecular formula of water gas $$= {H}_{2} + CO$$
    Combustion of $${H}_{2}$$-
    $${H}_{2} + \cfrac{1}{2} {O}_{2} \longrightarrow {H}_{2}O; \; \Delta{H} = 241.3 \; KJ$$
    Combustion of $$CO$$-
    $$CO + \cfrac{1}{2} {O}_{2} \longrightarrow C{O}_{2}; \; \Delta{H} = 283 \; KJ$$
    $$1$$ mole of $${H}_{2}$$ and $$CO$$ each gives,
    $$\Delta{H} = 283 + \left( 241.8 \right) = 524.8 \; KJ$$
    $$1$$ mole of $${H}_{2} = 22.4 \; L$$
    Similarly,
    $$1$$ mole of $$CO = 22.4 \; L$$
    $$\therefore$$ Total volume $$= 22.4 + 22.4 = 44.8 \; L$$
    Therefore,
    Heat evolved during combustion of $$44.8 \; L$$ of water gas $$= 524.8 \; KJ$$
    Heat evolved during combustion of $$112 \; L$$ of water gas $$= \cfrac{524.8 \times 112}{44.8} = 1312 \; KJ$$
    Hence the heat evolved during the combustion of $$112$$ litre of water gas at STP is $$1312 \; KJ$$.
  • Question 10
    1 / -0
    One mole of a real gas is subjected to a process from $$(2\ bar, 30\ lit, 300\ K)$$ to $$(2\ bar, 50\ lit, 400\ K)$$
    Given: $$C_{V} = 40\ J/mol\ K$$,
    $$C_{P} = 50\ J/mol/ K$$
    Calculate $$\Delta U$$.
    Solution
    Change in internal energy is written as:
    $$\Delta U = nC_v \Delta T$$
    $$\Delta U = 1\times 40\times (400-300)$$
    $$\Delta U = 4000J$$
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