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 :
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 :
`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
Text Solution
AI Generated Solution
The correct Answer is:
To determine whether the given reaction is supported by enthalpy, entropy, both, or neither, we can analyze the provided thermodynamic data:
1. **Given Data:**
- Reaction: \( \text{CH}_2=\text{CH}_2(g) + \text{Cl}_2(g) \rightarrow \text{ClCH}_2\text{CH}_2\text{Cl}(g) \)
- \( \Delta_r H^\circ = -217.5 \, \text{kJ/mol} \)
- \( \Delta_r S^\circ = -233.9 \, \text{J/(K·mol)} \)
2. **Understanding Spontaneity:**
- A reaction is spontaneous if the Gibbs free energy change (\( \Delta G \)) is negative.
- The relationship between Gibbs free energy, enthalpy, and entropy is given by:
\[
\Delta G = \Delta H - T \Delta S
\]
- For spontaneity, we need \( \Delta G < 0 \).
3. **Analyzing Enthalpy (\( \Delta H \)):**
- The value of \( \Delta H \) is negative (\( -217.5 \, \text{kJ/mol} \)), indicating that the reaction is exothermic. This contributes favorably to spontaneity.
4. **Analyzing Entropy (\( \Delta S \)):**
- The value of \( \Delta S \) is negative (\( -233.9 \, \text{J/(K·mol)} \)). A negative entropy change suggests that the disorder of the system decreases, which does not favor spontaneity.
5. **Determining Gibbs Free Energy (\( \Delta G \)):**
- To assess whether \( \Delta G \) is negative, we can substitute the values into the Gibbs free energy equation:
\[
\Delta G = -217.5 \times 10^3 \, \text{J/mol} - T \times (-233.9) \, \text{J/(K·mol)}
\]
- Rearranging gives:
\[
\Delta G = -217500 + 233.9T
\]
- The sign of \( \Delta G \) will depend on the temperature \( T \). At sufficiently low temperatures, the negative term \( -217500 \) will dominate, making \( \Delta G < 0 \).
6. **Conclusion:**
- Since \( \Delta H \) is negative (favorable) and \( \Delta S \) is negative (unfavorable), the reaction is supported by enthalpy but not by entropy. Therefore, the correct answer is that the reaction is supported by enthalpy.
### Final Answer:
The reaction is supported by enthalpy.
To determine whether the given reaction is supported by enthalpy, entropy, both, or neither, we can analyze the provided thermodynamic data:
1. **Given Data:**
- Reaction: \( \text{CH}_2=\text{CH}_2(g) + \text{Cl}_2(g) \rightarrow \text{ClCH}_2\text{CH}_2\text{Cl}(g) \)
- \( \Delta_r H^\circ = -217.5 \, \text{kJ/mol} \)
- \( \Delta_r S^\circ = -233.9 \, \text{J/(K·mol)} \)
2. **Understanding Spontaneity:**
...
Topper's Solved these Questions
Similar Questions
Explore conceptually related problems
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
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 )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 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 :
Calculate the equilibrium constant, K for the following reaction at 400K? 2NOCl_((g))iff2NO_((g))+Cl_(2(g)) Given that Delta_(r)H^(0)=80.0KJmol^(-1) and Delta_(r)S^(0)=120JK^(-1)mol^(-1) at 400 K.