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DeltaG=DeltaH-TDeltaS and ltBRgt DeltaG...

`DeltaG=DeltaH-TDeltaS` and ltBRgt `DeltaG=DeltaH+T[(d(DeltaG))/(dT)]_(p),` then` ((dE_(cell))/(dT))` is

A

`(DeltaS)/(nF)`

B

`(nE)/(DeltaS)`

C

`-nFE_(cell)`

D

`nFE_(cell)`

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The correct Answer is:
To solve the problem step-by-step, we will analyze the given equations and derive the required expression for \(\frac{dE_{cell}}{dT}\). ### Step 1: Understand the given equations We have two equations: 1. \(\Delta G = \Delta H - T \Delta S\) 2. \(\Delta G = \Delta H + T \left(\frac{d(\Delta G)}{dT}\right)_{p}\) ### Step 2: Set the equations equal to each other Since both expressions are equal to \(\Delta G\), we can set them equal to each other: \[ \Delta H - T \Delta S = \Delta H + T \left(\frac{d(\Delta G)}{dT}\right)_{p} \] ### Step 3: Cancel out \(\Delta H\) Subtract \(\Delta H\) from both sides: \[ -T \Delta S = T \left(\frac{d(\Delta G)}{dT}\right)_{p} \] ### Step 4: Divide by T Assuming \(T \neq 0\), divide both sides by \(T\): \[ -\Delta S = \left(\frac{d(\Delta G)}{dT}\right)_{p} \] ### Step 5: Relate \(\Delta S\) to \(\frac{dE_{cell}}{dT}\) From thermodynamics, we know that: \[ \Delta S = nF \left(\frac{dE_{cell}}{dT}\right) \] Thus, we can substitute this into our equation: \[ -\Delta S = -nF \left(\frac{dE_{cell}}{dT}\right) \] ### Step 6: Rearranging the equation This gives us: \[ \left(\frac{dE_{cell}}{dT}\right) = \frac{\Delta S}{nF} \] ### Conclusion Thus, the final expression for \(\frac{dE_{cell}}{dT}\) is: \[ \frac{dE_{cell}}{dT} = \frac{\Delta S}{nF} \] ### Final Answer The correct option is: \[ \frac{\Delta S}{nF} \] ---

To solve the problem step-by-step, we will analyze the given equations and derive the required expression for \(\frac{dE_{cell}}{dT}\). ### Step 1: Understand the given equations We have two equations: 1. \(\Delta G = \Delta H - T \Delta S\) 2. \(\Delta G = \Delta H + T \left(\frac{d(\Delta G)}{dT}\right)_{p}\) ### Step 2: Set the equations equal to each other ...
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DeltaG=DeltaH-TDeltaS and DeltaG=DeltaH+T[(d(DeltaG))/(dT)]_(p), then ((dE_(cell))/(dT)) is

Derive the equation, DeltaG = DeltaH - T DeltaS .

What is significance of T DeltaS in DeltaG = DeltaH - T DeltaS ?

The cell potential (E_(cell)) of a reaction is related as /_\G=-nF E_(cell) , where /_\G represents max. useful electrical work n=no. of moles of electrons exchanged during the section for reversible cell reaction d(/_\G)=(/_\_rV)dp-(/_\_rS),dT at constant pressure d(/_\G)=-(/_\_rS).dT :' At constant pressure /_\G=/_\H-T./_\S :. /_\G=H+T(d(/_\G))/((dT)_P) ((dE_(cell))/(dT))_P is known as temperture coefficient of the e.m.f of the cell. The temperature coefficient of the e.m.f of cell, ((dE)/(dT))_P si given by:

Which of the following is true during adsorption? a. DeltaG , DeltaH , and DeltaS all are negative. b. DeltaG is negative, but DeltaH and DeltaS is positive. c. DeltaG and DeltaH are negative, but DeltaS is positive. d. DeltaG and DeltaS are negative, but DeltaH is positive.

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

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

A contributions of both heat (enthalpy) and randomness(entropy) shall be considered to the overall spontaneity of process.When deciding about the spontaneity of a chemical reaction or other process, we define a quantity called the Gibb's energy change (DeltaG) . DeltaG=DeltaH-TDeltaS where, DeltaH =Enthalpy change, DeltaS =Entropy change , T=Temperature in kelvin. If DeltaGlt0 , Process is spontaneous , DeltaG=0 , Process is at equilibrium , DeltaGgt0 , Process is non-spontaneous. 5 mol of liquid water is compressed from 1 bar to 10 bar at constant temperature.Change is Gibb's energy (DeltaG) in Joule is:[Density of water = 1000 kg//m^3 ]

A contributions of both heat (enthalpy) and randomness(entropy) shall be considered to the overall spontaneity of process.When deciding about the spontaneity of a chemical reaction or other process, we define a quantity called the Gibb's energy change (DeltaG) . DeltaG=DeltaH-TDeltaS where, DeltaH =Enthalpy change, DeltaS =Entropy change , T=Temperature in kelvin. If DeltaGlt0 , Process is spontaneous , DeltaG=0 , Process is at equilibrium , DeltaGgt0 , Process is non-spontaneous. For the change H_2O(s),(273 K ,2 atm) to H_2O(l) ,(273 K, 2 atm), choose the correct option.

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

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