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Consider the following reaction at tempe...

Consider the following reaction at temperature T :
`CH_(2)=CH_(2)(g) +Cl_(2)(g)rarrClCH_(2)CH_(2)Cl(g)`
`Delta_(r ) H^(@)=-217.5kJ//"mol, " Delta_(r )S^(@)=-233.9J//K-"mol"`
Reaction is supported by :

A

entropy enthalpy

B

enthalpy

C

both (a) & (b)

D

neither

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The correct Answer is:
To determine the driving force behind the reaction \( \text{CH}_2=\text{CH}_2(g) + \text{Cl}_2(g) \rightarrow \text{ClCH}_2\text{CH}_2\text{Cl}(g) \) with given values of \( \Delta_r H^\circ = -217.5 \, \text{kJ/mol} \) and \( \Delta_r S^\circ = -233.9 \, \text{J/K} \cdot \text{mol} \), we can analyze the spontaneity of the reaction using Gibbs free energy (\( \Delta G \)). ### Step-by-Step Solution: 1. **Identify the Gibbs Free Energy Equation**: The Gibbs free energy change (\( \Delta G \)) for a reaction is given by the equation: \[ \Delta G = \Delta H - T \Delta S \] 2. **Determine the Sign of \( \Delta H \)**: From the given data, \( \Delta_r H^\circ = -217.5 \, \text{kJ/mol} \). A negative \( \Delta H \) indicates that the reaction is exothermic, which favors spontaneity. 3. **Determine the Sign of \( \Delta S \)**: The given value for entropy change is \( \Delta_r S^\circ = -233.9 \, \text{J/K} \cdot \text{mol} \). A negative \( \Delta S \) suggests that the disorder of the system decreases, which does not favor spontaneity. 4. **Analyze the Conditions for Spontaneity**: For the reaction to be spontaneous, \( \Delta G \) must be negative. Since \( \Delta H \) is negative (favorable) and \( \Delta S \) is negative (unfavorable), we need to consider the temperature \( T \): - If \( T \Delta S \) is sufficiently large and positive, it can make \( \Delta G \) positive, thus making the reaction non-spontaneous at high temperatures. - Conversely, at low temperatures, the negative \( \Delta H \) can dominate, making \( \Delta G \) negative and the reaction spontaneous. 5. **Conclusion**: Since the reaction has a negative enthalpy change and a negative entropy change, it is supported by enthalpy. Therefore, the reaction is spontaneous at lower temperatures where the enthalpy effect outweighs the entropy effect. ### Final Answer: The reaction is supported by **enthalpy**.

To determine the driving force behind the reaction \( \text{CH}_2=\text{CH}_2(g) + \text{Cl}_2(g) \rightarrow \text{ClCH}_2\text{CH}_2\text{Cl}(g) \) with given values of \( \Delta_r H^\circ = -217.5 \, \text{kJ/mol} \) and \( \Delta_r S^\circ = -233.9 \, \text{J/K} \cdot \text{mol} \), we can analyze the spontaneity of the reaction using Gibbs free energy (\( \Delta G \)). ### Step-by-Step Solution: 1. **Identify the Gibbs Free Energy Equation**: The Gibbs free energy change (\( \Delta G \)) for a reaction is given by the equation: \[ \Delta G = \Delta H - T \Delta S ...
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Determine the enthalpy of formation of B_(2)H_(6) (g) in kJ/mol of the following reaction : B_(2)H_(6)(g)+3O_(2)(g)rarrB_(2)O_(3)(s)+3H_(2)O(g) , Given : Delta_(r )H^(@)=-1941 " kJ"//"mol", " "DeltaH_(f)^(@)(B_(2)O_(3),s)=-1273" kJ"//"mol," DeltaH_(f)^(@)(H_(2)O,g)=-241.8 " kJ"//"mol"

Calculate Delta_(r)S_("sys")^(@) for the following reaction at 373 K: CO(g) + H_(2)O(g) to CO_(2)(g) + H_(2)(g) Delta_(r)H^(@) = -4.1 xx 10^(4) J, Delta_(r)S^(@)("unv") = 56 J//K

Consider the following reaction : CO(g)+2H_(2)(g)iffCH_(3)OH(g) Given : Delta_(f)H^(@)(CH_(3)OH,g)=-201 " kJ"//"mol", " "Delta_(f)H^(@)(CO,g)=-114" kJ"//"mol" S^(@)(CH_(3)OH,g)=240" J"//"K-mol, "S^(@)(H_(2),g)=29" JK"^(-1)" mol"^(-1) S^(@)(CO,g)=198 " J"//"mol-K, "C_(p,m)^(@)(H_(2))=28.8 " J"//"mol-K" C_(p,m)^(@)(CO)=29.4 " J"//"mol-K, "C_(p,m)^(@)(CH_(3)OH)=44 " J"//"mol-K" and " "ln ((320)/(300))=0.06 , all data at 300 K Delta_(r )G^(@) at 320 K is :

Standard Gibb's energy of reaction (Delta_(r )G^(@)) at a certain temperature can be computed Delta_(r )G^(@)=Delta_(r)H^(@)-T.Delta_(r )S^(@) and the change in the value of Delta_(r)H^(@) and Delta_(r)S^(@) for a reaction with temperature can be computed as follows : Delta_(r )H_(T_(2))^(@)-Delta_(r )H_(T_(1))^(@)=Delta_(r )C_(p)^(@)(T_(2)-T_(1)) Delta_(r )S_(T_(2))^(@)-Delta_(r )S_(T_(1))^(@)=Delta_(r )C_(p)^(@)ln.(T_(2)/T_(1)) " "Delta_(r )G^(@)=Delta_(r)H^(@)-T.Delta_(r)S^(@) and " by "Delta_(r )G^(@)=-"RT " ln K_(eq) . Consider the following reaction : CO(g)+2H_(2)(g)iffCH_(3)OH(g) Given : Delta_(f)H^(@)(CH_(3)OH,g)=-201 " kJ"//"mol", " "Delta_(f)H^(@)(CO,g)=-114" kJ"//"mol" S^(@)(CH_(3)OH,g)=240" J"//"K-mol, "S^(@)(H_(2),g)=29" JK"^(-1)" mol"^(-1) S^(@)(CO,g)=198 " J"//"mol-K, "C_(p,m)^(@)(H_(2))=28.8 " J"//"mol-K" C_(p,m)^(@)(CO)=29.4 " J"//"mol-K, "C_(p,m)^(@)(CH_(3)OH)=44 " J"//"mol-K" and " "ln ((320)/(300))=0.06 , all data at 300 K Delta_(r )S^(@) at 300 K for the reaction is :

Standard Gibb's energy of reaction (Delta_(r )G^(@)) at a certain temperature can be computed Delta_(r )G^(@)=Delta_(r)H^(@)-T.Delta_(r )S^(@) and the change in the value of Delta_(r)H^(@) and Delta_(r)S^(@) for a reaction with temperature can be computed as follows : Delta_(r )H_(T_(2))^(@)-Delta_(r )H_(T_(1))^(@)=Delta_(r )C_(p)^(@)(T_(2)-T_(1)) Delta_(r )S_(T_(2))^(@)-Delta_(r )S_(T_(1))^(@)=Delta_(r )C_(p)^(@)ln.(T_(2)/T_(1)) " "Delta_(r )G^(@)=Delta_(r)H^(@)-T.Delta_(r)S^(@) and " by "Delta_(r )G^(@)=-"RT " ln K_(eq) . Consider the following reaction : CO(g)+2H_(2)(g)iffCH_(3)OH(g) Given : Delta_(f)H^(@)(CH_(3)OH,g)=-201 " kJ"//"mol", " "Delta_(f)H^(@)(CO,g)=-114" kJ"//"mol" S^(@)(CH_(3)OH,g)=240" J"//"K-mol, "S^(@)(H_(2),g)=29" JK"^(-1)" mol"^(-1) S^(@)(CO,g)=198 " J"//"mol-K, "C_(p,m)^(@)(H_(2))=28.8 " J"//"mol-K" C_(p,m)^(@)(CO)=29.4 " J"//"mol-K, "C_(p,m)^(@)(CH_(3)OH)=44 " J"//"mol-K" and " "ln ((320)/(300))=0.06 , all data at 300 K Delta_(r )H^(@) at 300 K for the reaction is :

Standard Gibb's energy of reaction (Delta_(r )G^(@)) at a certain temperature can be computed Delta_(r )G^(@)=Delta_(r)H^(@)-T.Delta_(r )S^(@) and the change in the value of Delta_(r)H^(@) and Delta_(r)S^(@) for a reaction with temperature can be computed as follows : Delta_(r )H_(T_(2))^(@)-Delta_(r )H_(T_(1))^(@)=Delta_(r )C_(p)^(@)(T_(2)-T_(1)) Delta_(r )S_(T_(2))^(@)-Delta_(r )S_(T_(1))^(@)=Delta_(r )C_(p)^(@)ln.(T_(2)/T_(1)) " "Delta_(r )G^(@)=Delta_(r)H^(@)-T.Delta_(r)S^(@) and " by "Delta_(r )G^(@)=-"RT " ln K_(eq) . Consider the following reaction : CO(g)+2H_(2)(g)iffCH_(3)OH(g) Given : Delta_(f)H^(@)(CH_(3)OH,g)=-201 " kJ"//"mol", " "Delta_(f)H^(@)(CO,g)=-114" kJ"//"mol" S^(@)(CH_(3)OH,g)=240" J"//"K-mol, "S^(@)(H_(2),g)=29" JK"^(-1)" mol"^(-1) S^(@)(CO,g)=198 " J"//"mol-K, "C_(p,m)^(@)(H_(2))=28.8 " J"//"mol-K" C_(p,m)^(@)(CO)=29.4 " J"//"mol-K, "C_(p,m)^(@)(CH_(3)OH)=44 " J"//"mol-K" and " "ln ((320)/(300))=0.06 , all data at 300 K Delta_(r )S^(@) at 320 K is :

Standard Gibb's energy of reaction (Delta_(r )G^(@)) at a certain temperature can be computed Delta_(r )G^(@)=Delta_(r)H^(@)-T.Delta_(r )S^(@) and the change in the value of Delta_(r)H^(@) and Delta_(r)S^(@) for a reaction with temperature can be computed as follows : Delta_(r )H_(T_(2))^(@)-Delta_(r )H_(T_(1))^(@)=Delta_(r )C_(p)^(@)(T_(2)-T_(1)) Delta_(r )S_(T_(2))^(@)-Delta_(r )S_(T_(1))^(@)=Delta_(r )C_(p)^(@)ln.(T_(2)/T_(1)) " "Delta_(r )G^(@)=Delta_(r)H^(@)-T.Delta_(r)S^(@) and " by "Delta_(r )G^(@)=-"RT " ln K_(eq) . Consider the following reaction : CO(g)+2H_(2)(g)iffCH_(3)OH(g) Given : Delta_(f)H^(@)(CH_(3)OH,g)=-201 " kJ"//"mol", " "Delta_(f)H^(@)(CO,g)=-114" kJ"//"mol" S^(@)(CH_(3)OH,g)=240" J"//"K-mol, "S^(@)(H_(2),g)=29" JK"^(-1)" mol"^(-1) S^(@)(CO,g)=198 " J"//"mol-K, "C_(p,m)^(@)(H_(2))=28.8 " J"//"mol-K" C_(p,m)^(@)(CO)=29.4 " J"//"mol-K, "C_(p,m)^(@)(CH_(3)OH)=44 " J"//"mol-K" and " "ln ((320)/(300))=0.06 , all data at 300 K Delta_(r )H^(@) at 320 K is :

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NARENDRA AWASTHI ENGLISH-THERMODYNAMICS-Level 3
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  7. If the boundary of system moves by an infinitesimal amount, the work i...

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  8. Standard Gibb's energy of reaction (Delta(r )G^(@)) at a certain temp...

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  9. Standard Gibb's energy of reaction (Delta(r )G^(@)) at a certain temp...

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  10. Standard Gibb's energy of reaction (Delta(r )G^(@)) at a certain temp...

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  11. Standard Gibb's energy of reaction (Delta(r )G^(@)) at a certain temp...

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  12. Consider the following reaction : CO(g)+2H(2)(g)iffCH(3)OH(g) Give...

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  13. Enthalpy of neutralization is defined as the enthalpy change when 1 mo...

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  14. Enthalpy of neutralzation is defined as the enthalpy change when 1 mol...

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  15. Enthalpy of neutralzation is defined as the enthalpy change when 1 mol...

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  16. Gibbs Helmholtz equation relates the enthalpy, entropy and free energy...

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  17. Gibbs Helmholtz equation relates the enthalpy, entropy and free energy...

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  18. Gibbs Helmholtz equation relates the enthalpy, entropy and free energy...

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  20. Identify the extensive quantities from the following :

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  21. Identify the state functions from the following :

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