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Show that R=8.314 Jmol^(-1)K^(-1)...

Show that R=8.314 `Jmol^(-1)K^(-1)`

Text Solution

Verified by Experts

We know that `(PV)/T=R`
At normal temperature `P_0=1atm=1.013xx10^5Nm^(-2),V_0=0.0224m^3` and `T_0=273K`
Hence `R=((1.013xx10^5)(0.0224))/(273)=8.314Jmol^(-1)K^(-1)`
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In general it is observed that the rate of a chemical reaction doubles with every 10 degree rise in temperature. If the generalization holds good for the reaction in the temperature range 295 K to 305 K, what would be the value of activation energy for this reaction ? [R = 8.314 mol^(-1)JK^(-1)]

What is the value of the equilibrium constant for the following reaction at 400 K ? 2NOCl(g) hArr 2NO(g) + Cl_(2)(g) Delta H^(@) = 77.5 kJ mol^(-1), R = 8.3124 J mol^(-1) K^(-1), Delta S = 135 J K^(-1) mol^(-1) .

Knowledge Check

  • Two reaction R_1 and R_2 have identical pr-exponential factor. Activation energy of R_1 exceeds that of R_2 by 10 kJ mol^(-1) . If k_1 and k_2 re rate constant for reactions R_1 and R_2 respectively at 300 K, then ln (k_2//k_1) is equal to : (R=8cdot314 J mol ^(-1) K^(-1)

    A
    8
    B
    6
    C
    12
    D
    4
  • What is the activation energy for a reaction if the rate is doubled when the temperature is raised from 20^@C to 35^@C (R= 8 cdot 314 J mol^(-1) K^(-1)) .

    A
    `15 cdot 1 kJ mol^(-1)
    B
    342 kJ mol^(-1)`
    C
    `269 k Jmol^(-1)`
    D
    `34 cdot 7 kJ mol^(-1)
  • Assuming that water vapour is an ideal gas, the internal energy changes (Delta U) when 1 mol 100^@C (Given molar enthalpy of vaporization of water at 1 bar and 373 k = 41 k J mol^(-1) and R= 8 cdot 3 J mol^(-1) K^(-1) ) will be

    A
    `3. cdot 7904 k J mol^(-1)`
    B
    `37. cdot 904 k J mol^(-1)`
    C
    `41. cdot 00 k J mol^(-1)`
    D
    `4. cdot 100 k J mol^(-1)`
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    The ratio of specific heats of a gas in 1.40 . There are 200 moles of gas initially present. The gas undergoes adiabatic expansion and as a result which, the temperature of the gas falls from 400 K to 100 K. Give R=8.312J "mole"^(-1) K^(-1) . Calculate the amount or work done by the gas on the surroundings.

    The rate constant of a first order reaction at 300 K and 310 K are respectively 1.2 xx 10^(3) s^(-1) and 2.4 xx 10^(3) s^(-1) . Calculate the energy of activation. (R = 8.314 J K^(-1) mol^(-1))

    For the equilibirum, PCl_(5)(g) hArr PCl_(3)(g) + Cl_(2)(g) at 298 K, K = 1.8 xx 10^(-7) . Calculate Delta G^(@) for the reaction (R = 8.314 JK^(-1) mol^(-1)) .

    If equilibrium constant K is 10^(3) , the Delta G^(theta) for the reaction at 300 K is (assume R = 8.314 JK^(-1) mol^(-1) ) :