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Gibbs Helmholtz equation relates the ent...

Gibbs Helmholtz equation relates the enthalpy, entropy and free energy change of the process at constant pressure and temperature as
`DeltaG=DeltaH-TDeltaS " (at constant P, T)"`
In General the magnitude of `DeltaH` does not change much with the change in temperature but the terms `TDeltaS` changes appreciably. Hence in some process spontaneity is very much dependent on temperature and such processes are generally known as entropy driven process.
When `CaCO_(3)` is heated to a high temperature it decomposes into CaO and `CO_(2)`, however it is quite stable at room temperature. It can be explained by the fact that

A

`Delta_(r )H` dominates the term `TDeltaS` at high temperature

B

the term `TDeltaS` dominates the `Delta_(r )H` at high temperature

C

at high temperature both `Delta_(r )S` and `Delta_(r )H` becomes negative

D

thermodynamics can not say anything about spontaneity

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To explain why calcium carbonate (CaCO₃) is stable at room temperature but decomposes into calcium oxide (CaO) and carbon dioxide (CO₂) when heated, we can analyze the situation using the Gibbs-Helmholtz equation: ### Step-by-Step Solution: 1. **Understanding the Gibbs-Helmholtz Equation**: The Gibbs-Helmholtz equation is given by: \[ \Delta G = \Delta H - T\Delta S \] where: - \(\Delta G\) = change in Gibbs free energy - \(\Delta H\) = change in enthalpy - \(T\) = absolute temperature - \(\Delta S\) = change in entropy 2. **Analyzing Stability at Room Temperature**: At room temperature, the decomposition of CaCO₃ into CaO and CO₂ is not spontaneous. This means that: \[ \Delta G > 0 \] This indicates that the reaction does not proceed under these conditions. 3. **Considering the Changes in Enthalpy and Entropy**: - The decomposition reaction can be represented as: \[ \text{CaCO}_3 (s) \rightarrow \text{CaO} (s) + \text{CO}_2 (g) \] - Generally, the change in enthalpy (\(\Delta H\)) for this reaction is positive (endothermic), meaning energy is required to break the bonds in CaCO₃. - The change in entropy (\(\Delta S\)) is positive because the products (CaO and CO₂) have more disorder than the reactant (solid CaCO₃). 4. **Effect of Temperature on Spontaneity**: As the temperature increases, the term \(T\Delta S\) becomes larger. Since \(\Delta S\) is positive, \(T\Delta S\) will also be positive and can outweigh the positive \(\Delta H\): \[ \Delta G = \Delta H - T\Delta S \] At high temperatures, if \(T\Delta S\) becomes greater than \(\Delta H\), then: \[ \Delta G < 0 \] This indicates that the reaction becomes spontaneous at high temperatures. 5. **Conclusion**: Therefore, the stability of CaCO₃ at room temperature can be attributed to the fact that the positive \(\Delta H\) and the relatively lower temperature do not favor the decomposition reaction. However, at high temperatures, the entropy term dominates, making the reaction spontaneous.

To explain why calcium carbonate (CaCO₃) is stable at room temperature but decomposes into calcium oxide (CaO) and carbon dioxide (CO₂) when heated, we can analyze the situation using the Gibbs-Helmholtz equation: ### Step-by-Step Solution: 1. **Understanding the Gibbs-Helmholtz Equation**: The Gibbs-Helmholtz equation is given by: \[ \Delta G = \Delta H - T\Delta S ...
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Gibbs Helmholtz equation relates the enthalpy, entropy and free energy change of the process at constant pressure and temperature as DeltaG=DeltaH-TDeltaS " (at constant P, T)" In General the magnitude of DeltaH does not change much with the change in temperature but the terms TDeltaS changes appreciably. Hence in some process spontaneity is very much dependent on temperature and such processes are generally known as entropy driven process. Fro the reaction at 298 K, A_(2)B_(4)rarr2AB_(2) DeltaH=2" kJ" and DeltaS = 20 J/K at constant P and T, the reaction will be

Gibbs Helmholtz equation relates the enthalpy, entropy and free energy change of the process at constant pressure and temperature as DeltaG=DeltaH-TDeltaS " (at constant P, T)" In General the magnitude of DeltaH does not change much with the change in temperature but the terms TDeltaS changes appreciably. Hence in some process spontaneity is very much dependent on temperature and such processes are generally known as entropy driven process. The Dissolution of CaCl_(2).6H_(2)O in a large volume of water is endothermic to the extent of 3.5 kcal "mol"^(-1) and DeltaH for the reaction is -23.2 kcal "mol"^(-1) . CaCl_(2)(s)+6H_(2)O(l)rarrCaCl_(2).6H_(2)O(s) Select the correct statement :

Free energy change for a reversible process is

Gibbs-Helmoholtz equation relates the free energy change to the enthalpy and entropy changes of the process as (DeltaG)_(PT) = DeltaH - T DeltaS The magnitude of DeltaH does not change much with the change in temperature but the energy factor T DeltaS changes appreciably. Thus, spontaneity of a process depends very much on temperature. A reaction has value of DeltaH = 20 kcal at 200K , the reaction is spontaneous, below this temperature, it is not. the values DeltaG and DeltaS at 200K are, respectively

Gibbs-Helmoholtz equation relates the free energy change to the enthalpy and entropy changes of the process as (DeltaG)_(PT) = DeltaH - T DeltaS The magnitude of DeltaH does not change much with the change in temperature but the energy factor T DeltaS changes appreciably. Thus, spontaneity of a process depends very much on temperature. For the reaction at 25^(0)C, X_(2)O_(4)(l) rarr 2XO_(2) DeltaH = 2.0 kcal and DeltaS = 20 cal K^(-1) . the reaction would be

During the micelle formation how the enthalpy entropy and Gibbes energy change?

Gibbs-Helmoholtz equation relates the free energy change to the enthalpy and entropy changes of the process as (DeltaG)_(PT) = DeltaH - T DeltaS The magnitude of DeltaH does not change much with the change in temperature but the enrgy factor T DeltaS changes appreciably. Thus, spontaneity of a process depends very much on temperature. For the reaction at 298K, 2A +B rarr C DeltaH = 100 kcal and DeltaS = 0.020 kcal K^(-1) . If DeltaH and DeltaS are assumed to be constant over the temperature range, at what temperature will the reaction become spontaneous?

Dependence of Spontaneity on Temperature: For a process to be spontaneous , at constant temperature and pressure , there must be decrease in free energy of the system in the direction of the process , i.e. DeltaG_(P.T) lt 0. DeltaG_(P.T) =0 implies the equilibrium condition and DeltaG_(P.T) gt 0 corresponds to non- spontaneity. Gibbs- Helmholtz equation relates the free energy change to the enthalpy and entropy changes of the process as : " "DeltaG_(P.T) = DeltaH-TDeltaS" ""..."(1) The magnitude of DeltaH does not change much with the change in temperature but the entropy factor TDeltaS change appreciably . Thus, spontaneity of a process depends very much on temperature. For endothermic process, both DeltaH and DeltaS are positive . The energy factor, the first factor of equation, opposes the spontaneity whereas entorpy factor favours it. At low temperature the favourable factor TDeltaS will be small and may be less than DeltaH, DeltaG will have positive value indicated the nonspontaneity of the process. On raising temperature , the factor TDeltaS Increases appreciably and when it exceeds DeltaH, DeltaG would become negative and the process would be spontaneous . For an expthermic process, both DeltaH and DeltaS would be negative . In this case the first factor of eq.1 favours the spontaneity whereas the second factor opposes it. At high temperature , when T DeltaS gt DeltaH, DeltaG will have positive value, showing thereby the non-spontaneity fo the process . However , on decreasing temperature , the factor , TDeltaS decreases rapidly and when TDeltaS lt DeltaH, DeltaG becomes negative and the process occurs spontaneously. Thus , an exothermic process may be spontaneous at low temperature and non-spontaneous at high temperature. The enthalpy change for a certain rection at 300 K is -15.0 K cal mol^(-1) . The entropy change under these conditions is -7.2 cal K^(-1)mol^(-1) . The free energy change for the reaction and its spontaneous/ non-spontaneous character will be

Dependence of Spontaneity on Temperature: For a process to be spontaneous , at constant temperature and pressure , there must be decrease in free energy of the system in the direction of the process , i.e. DeltaG_(P.T) lt 0. DeltaG_(P.T) =0 implies the equilibrium condition and DeltaG_(P.T) gt 0 corresponds to non- spontaneity. Gibbs- Helmholtz equation relates the free energy change to the enthalpy and entropy changes of the process as : " "DeltaG_(P.T) = DeltaH-TDeltaS" ""..."(1) The magnitude of DeltaH does not change much with the change in temperature but the entropy factor TDeltaS change appreciably . Thus, spontaneity of a process depends very much on temperature. For endothermic process, both DeltaH and DeltaS are positive . The energy factor, the first factor of equation, opposes the spontaneity whereas entorpy factor favours it. At low temperature the favourable factor TDeltaS will be small and may be less than DeltaH, DeltaG will have positive value indicated the nonspontaneity of the process. On raising temperature , the factor TDeltaS Increases appreciably and when it exceeds DeltaH, DeltaG would become negative and the process would be spontaneous . For an expthermic process, both DeltaH and DeltaS would be negative . In this case the first factor of eq.1 favours the spontaneity whereas the second factor opposes it. At high temperature , when T DeltaS gt DeltaH, DeltaG will have positive value, showing thereby the non-spontaneity fo the process . However , on decreasing temperature , the factor , TDeltaS decreases rapidly and when TDeltaS lt DeltaH, DeltaG becomes negative and the process occurs spontaneously. Thus , an exothermic process may be spontaneous at low temperature and non-spontaneous at high temperature. For the reaction at 298 K ,2A + B rarr C DeltaH =100 kcal and DeltaS=0.050 kcal K^(-1) . If DeltaH and DeltaS are assumed to be constant over the temperature range, above what temperature will the reaction become spontaneous?

Dependence of Spontaneity on Temperature: For a process to be spontaneous , at constant temperature and pressure , there must be decrease in free energy of the system in the direction of the process , i.e. DeltaG_(P.T) lt 0. DeltaG_(P.T) =0 implies the equilibrium condition and DeltaG_(P.T) gt 0 corresponds to non- spontaneity. Gibbs- Helmholtz equation relates the free energy change to the enthalpy and entropy changes of the process as : " "DeltaG_(P.T) = DeltaH-TDeltaS" ""..."(1) The magnitude of DeltaH does not change much with the change in temperature but the entropy factor TDeltaS change appreciably . Thus, spontaneity of a process depends very much on temperature. For endothermic process, both DeltaH and DeltaS are positive . The energy factor, the first factor of equation, opposes the spontaneity whereas entorpy factor favours it. At low temperature the favourable factor TDeltaS will be small and may be less than DeltaH, DeltaG will have positive value indicated the nonspontaneity of the process. On raising temperature , the factor TDeltaS Increases appreciably and when it exceeds DeltaH, DeltaG would become negative and the process would be spontaneous . For an expthermic process, both DeltaH and DeltaS would be negative . In this case the first factor of eq.1 favours the spontaneity whereas the second factor opposes it. At high temperature , when T DeltaS gt DeltaH, DeltaG will have positive value, showing thereby the non-spontaneity fo the process . However , on decreasing temperature , the factor , TDeltaS decreases rapidly and when TDeltaS lt DeltaH, DeltaG becomes negative and the process occurs spontaneously. Thus , an exothermic process may be spontaneous at low temperature and non-spontaneous at high temperature. A reaction has a value of DeltaH =-40 Kcal at 400 k cal mol^(-1) . The reaction is spontaneous, below this temperature , it is not . The values fo DeltaG and DeltaS at 400 k are respectively

NARENDRA AWASTHI ENGLISH-THERMODYNAMICS-Level 3
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