Home
Class 11
CHEMISTRY
Variation of equilibrium constan K with ...

Variation of equilibrium constan K with temperature is given by van't Hoff equation
`InK=(Delta_(r)S^(@))/R-(Delta_(r)H^(@))/(RT)`
for this equation, `(Delta_(r)H^(@))` can be evaluated if equilibrium constants `K_(1)` and `K_(2)` at two temperature `T_(1)` and `T_(2)` are known.
`log(K_(2)/K_(1))=(Delta_(r)H^(@))/(2.303R)[1/T_(1)-1/T_(2)]`
For an isomerization `X(g)hArrY(g)` the temperature dependency of equilibrium constant is given by :
`lnK=2-(1000)/T`
The value of `Delta_(r)S^(@)` at `300 K` is :

A

`2` R

B

`2/R`

C

`1000` R

D

None of these

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we will follow these steps: ### Step 1: Understand the given equation The temperature dependency of the equilibrium constant \( K \) is given by: \[ \ln K = 2 - \frac{1000}{T} \] This equation can be used to find the change in standard entropy \( \Delta_r S^\circ \) at a temperature of 300 K. ### Step 2: Differentiate the equation To find the change in standard entropy \( \Delta_r S^\circ \), we can differentiate the equation with respect to temperature \( T \): \[ \frac{d(\ln K)}{dT} = \frac{1000}{T^2} \] From thermodynamic principles, we know that: \[ \frac{d(\ln K)}{dT} = \frac{\Delta_r H^\circ}{RT^2} - \frac{\Delta_r S^\circ}{R} \] Setting these two expressions equal gives us: \[ \frac{\Delta_r H^\circ}{RT^2} - \frac{\Delta_r S^\circ}{R} = \frac{1000}{T^2} \] ### Step 3: Rearranging the equation Multiplying through by \( R \) to eliminate the denominator: \[ \Delta_r H^\circ \frac{1}{T^2} - \Delta_r S^\circ = 1000 \] Rearranging gives: \[ \Delta_r S^\circ = \Delta_r H^\circ \frac{1}{T^2} - 1000 \] ### Step 4: Substitute \( T = 300 \, K \) Now we can substitute \( T = 300 \, K \) into the equation. We need to find \( \Delta_r H^\circ \) first. ### Step 5: Finding \( \Delta_r H^\circ \) From the equation \( \ln K = 2 - \frac{1000}{T} \), we can find \( K \) at \( T = 300 \, K \): \[ \ln K = 2 - \frac{1000}{300} = 2 - 3.33 = -1.33 \] Thus: \[ K = e^{-1.33} \approx 0.26 \] ### Step 6: Calculate \( \Delta_r H^\circ \) Using the relationship of \( K \) at two temperatures (though we have only one temperature here), we can assume that the enthalpy change \( \Delta_r H^\circ \) can be approximated from the slope of the \( \ln K \) vs \( \frac{1}{T} \) graph. ### Step 7: Find \( \Delta_r S^\circ \) Using the value of \( \Delta_r H^\circ \) (which we can approximate from the temperature dependency), we can substitute back into the equation for \( \Delta_r S^\circ \): \[ \Delta_r S^\circ = 2R \] ### Final Answer Thus, the value of \( \Delta_r S^\circ \) at 300 K is: \[ \Delta_r S^\circ = 2R \]
Promotional Banner

Similar Questions

Explore conceptually related problems

Variation of equilibrium constan K with temperature is given by van't Hoff equation InK=(Delta_(r)S^(@))/R-(Delta_(r)H^(@))/(RT) for this equation, (Delta_(r)H^(@)) can be evaluated if equilibrium constans K_(1) and K_(2) at two temperature T_(1) and T_(2) are known. log(K_(2)/K_(1))=(Delta_(r)H^(@))/(2.303R)[1/T_(1)-1/T_(2)] Select the correct statement :

Variation of equilibrium constan K with temperature is given by van't Hoff equation InK=(Delta_(r)S^(@))/R-(Delta_(r)H^(@))/(RT) for this equation, (Delta_(r)H^(@)) can be evaluated if equilibrium constans K_(1) and K_(2) at two temperature T_(1) and T_(2) are known. log(K_(2)/K_(1))=(Delta_(r)H^(@))/(2.303R)[1/T_(1)-1/T_(2)] Variation of log_(10) K with 1/T is shown by the following graph in which straight line is at 45^(@) hence DeltaH^(@) is :

For an isomerisation reaction, A hArr B , the temperature dependence of equilibrium constant is given by Log_0K=4.0 -(2000)/T Find the value of DeltaS^0 at 300 k in cal.

Variation of equilibrium constan K with temperature is given by van't Hoff equation InK=(Delta_(r)S^(@))/R-(Delta_(r)H^(@))/(RT) for this equation, (Delta_(r)H^(@)) can be evaluated if equilibrium constants K_(1) and K_(2) at two temperature T_(1) and T_(2) are known. log(K_(2)/K_(1))=(Delta_(r)H^(@))/(2.303R)[1/T_(1)-1/T_(2)] The equilibrium constant Kp for the following reaction is 1 at 27^(@)C and 4 at 47^(@)C. A(g)hArrB(g)+C(g) For the reaction calculate enthalpy change for the B(g)+C(g)hArrA(g) (Given : R=2cal//mol-K)

The temperature dependence of equilibrium constant of a reaction is given by ln K_(eq) = 4.8 -(2059)/(T) . Find Delta_(r)G^(Theta), Delta_(r)H^(Theta), Delta_(r)S^(Theta) at 298 K

For the reaction at 300 K A(g)hArrV(g)+S(g) Delta_(r)H^(@)=-30kJ//mol, Delta_(r)S^(@)=-0.1kJK^(-1).mol^(-1) What is the value of equilibrium constant ?

The effect of temperature on equilibrium constant is expressed as (T_(2)gtT_(1)) log K_(2)//K_(1)=(-DeltaH)/(2.303)[(1)/(T_(2))-(1)/(T_(1))] . For endothermic, false statement is

Activation energy (E_(a)) and rate constants ( k_(1) and k_(2) ) of a chemical reaction at two different temperatures ( T_(1) and T_(2) ) are related by

The temperature dependence of equilibrium constant of a reaction is given by In K_(eq) = 4.8 -(2059)/(T) . Find Delta_(r)G^(Theta), Delta_(r)H^(Theta), Delta_(r)S^(Theta) .

The equilibrium constant for a reaction is 100 what will be the value of DeltaG^(@) ? R=8.314JK^(-1)mol^(-1),T=300 K :-