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If K(p) for a reaction is 0.1 at 27^(@)C...

If `K_(p)` for a reaction is 0.1 at `27^(@)C` the `K_(c )` of the reaction will be

A

can not be calculate as `Delta n_(g) ` is not given

B

`(K_(p))/( RT)`

C

`K_(p) RT`

D

`(K_(p))/( ( RT)^(2))`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem of finding \( K_c \) from the given \( K_p \) value, we need to use the relationship between \( K_p \) and \( K_c \). The equation that relates these two constants is: \[ K_p = K_c (RT)^{\Delta N} \] Where: - \( K_p \) is the equilibrium constant in terms of partial pressures. - \( K_c \) is the equilibrium constant in terms of concentrations. - \( R \) is the universal gas constant (0.0821 L·atm/(K·mol)). - \( T \) is the temperature in Kelvin. - \( \Delta N \) is the change in the number of moles of gas (moles of gaseous products - moles of gaseous reactants). ### Step-by-step Solution: 1. **Convert Temperature to Kelvin**: \[ T = 27^\circ C + 273.15 = 300.15 \, K \] 2. **Identify Given Values**: - \( K_p = 0.1 \) - \( R = 0.0821 \, L·atm/(K·mol) \) - \( T = 300.15 \, K \) 3. **Determine \( \Delta N \)**: Since \( \Delta N \) is not provided in the question, we cannot calculate \( K_c \) directly. However, we can express \( K_c \) in terms of \( K_p \) and \( \Delta N \): \[ K_c = \frac{K_p}{(RT)^{\Delta N}} \] 4. **Conclusion**: Without the value of \( \Delta N \), we cannot determine a specific value for \( K_c \). Therefore, the problem cannot be solved completely with the information given. ### Final Answer: Since \( \Delta N \) is not provided, we cannot determine \( K_c \). ---
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