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log Kp/Kc+log RT=0 is a relationship for...

log `K_p/K_c`+log RT=0 is a relationship for the reaction :

A

(A) `PCI_(5)hArrPCI_(3)+CI_(2)`

B

(B) `2SO_(2)+O_(2)hArr2SO_(3)`

C

(C) `H_(2)+1_(2)hArr2HI`

D

(D) `N_(2)+3H_(2)hArr2NH_(3)`

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To solve the question regarding the relationship \( \log \frac{K_p}{K_c} + \log RT = 0 \), we can follow these steps: ### Step 1: Rewrite the given equation Starting with the equation: \[ \log \frac{K_p}{K_c} + \log RT = 0 \] We can combine the logarithms using the property \( \log a + \log b = \log(ab) \): \[ \log \left( \frac{K_p}{K_c} \cdot RT \right) = 0 \] ### Step 2: Exponentiate both sides To eliminate the logarithm, we exponentiate both sides: \[ \frac{K_p}{K_c} \cdot RT = 10^0 \] Since \( 10^0 = 1 \), we have: \[ \frac{K_p}{K_c} \cdot RT = 1 \] ### Step 3: Rearrange the equation Rearranging gives us: \[ K_p = K_c \cdot RT \] ### Step 4: Relate to the change in moles The relationship \( K_p = K_c (RT)^{\Delta n} \) can be compared to our derived equation. Here, \( \Delta n \) is defined as the change in the number of moles of gas, calculated as: \[ \Delta n = \text{(moles of gaseous products)} - \text{(moles of gaseous reactants)} \] From our equation \( K_p = K_c \cdot RT \), we can see that \( \Delta n = 0 \) because: \[ K_p = K_c (RT)^0 \implies \Delta n = 0 \] ### Step 5: Identify the reaction We need to find a reaction where the change in moles of gas (\( \Delta n \)) is equal to 0. ### Step 6: Evaluate the options We will evaluate the given reactions to find one that has \( \Delta n = 0 \): 1. **Option A**: \( \text{PCl}_3 + \text{Cl}_2 \rightarrow \text{PCl}_5 \) - Reactants: 2 moles (1 PCl3 + 1 Cl2) - Products: 1 mole (1 PCl5) - \( \Delta n = 1 - 2 = -1 \) 2. **Option B**: \( \text{N}_2 + 3\text{H}_2 \rightarrow 2\text{NH}_3 \) - Reactants: 4 moles (1 N2 + 3 H2) - Products: 2 moles (2 NH3) - \( \Delta n = 2 - 4 = -2 \) 3. **Option C**: \( 2\text{CO} + \text{O}_2 \rightarrow 2\text{CO}_2 \) - Reactants: 3 moles (2 CO + 1 O2) - Products: 2 moles (2 CO2) - \( \Delta n = 2 - 3 = -1 \) 4. **Option D**: \( \text{H}_2 + \text{I}_2 \rightarrow 2\text{HI} \) - Reactants: 2 moles (1 H2 + 1 I2) - Products: 2 moles (2 HI) - \( \Delta n = 2 - 2 = 0 \) ### Conclusion The reaction that validates the relationship \( \log \frac{K_p}{K_c} + \log RT = 0 \) is: \[ \text{H}_2 + \text{I}_2 \rightarrow 2\text{HI} \]
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What is the relationship between K_p and K_c ?

For a reaction, aA+bBhArrcC+dD , the reaction quotient Q=([C]_(0)^(c)[D]_(0)^(d))/([A]_(0)^(a)[B]_(0)^(b)) , where [A]_(0) , [B]_(0) , [C]_(0) , [D]_(0) are initial concentrations. Also K_(c)=([C]^(c)[D]^(d))/([A]^(a)[B]^(b)) where [A] , [B] , [C] , [D] are equilibrium concentrations. The reaction proceeds in forward direction if Q lt K_(c) and in backward direction if Q gt K_(c) . The variation of K_(c) with temperature is given by: 2303log(K_(C_(2)))/(K_(C_(1)))=(DeltaH)/(R)[(T_(2)-T_(1))/(T_(1)T_(2))] . For gaseous phase reactions K_(p)=K_(c)(RT)^(Deltan) where Deltan= moles of gaseous products - moles of gaseous reactants. Also -DeltaG^(@)=2.303RT log_(10)K_(c) . The heat or reaction for an endothermic reaction, in equilibrium is 1200 cal , at constant volume is more than at constant pressure at 300 K . The ratio of K_(p)//K_(c) is:

Knowledge Check

  • We know that the relationship between K_(c)andK_(p) is K_(p)=K_(c)(RT)^(Deltan) What would be the value of Deltan for the reaction : NH_(4)Cl_((s))hArrNH_(3(g))+HCl_((g))?

    A
    1
    B
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    C
    1.5
    D
    2
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