The first order rate constant for the decomposition of `C_(2)H_(5)I` by the reaction. `C_(2)H_(5)I(g)rarrC_(2)H_(4)(g)+HI(g)` at `600 K is 1.60xx10^(-5)s^(-1)`. Its energy of activation is `209 kJ mol^(-1)`. Calculate the rate constant at `700 K`
The first order rate constant for the decomposition of ethyl iodide by the reaction. C_(2)H_(5)(g) to C_(2)H_(4)(g) + HI(g) at 600 K is 160 xx 10^(-5)s^(-1) , T_(1)= 600K , T_(2)=700K, E_(a) = 209 kJmol^(-1) . logk_(2)= log(1.60 xx 10^(-5)s^(-1)) + (209000Jmol^(-1))/(2.303 xx 8.314J mol^(-1)K^(-1))[1/(600K)-1/(700K)] log k_(2)=(-5 + 0.2041) + 2.5989 = -2.197 = bar3.8080 k_(2)="Antilog" bar3.8030 = 6.36 xx 10^(-3)s^(-1)
The first order rate constant for the decomposition of CaCO_3 , at 700 K is 6.36 xx 10^(-3)s^(-1) and activation energy is 209 "kJ mol"^(-1) . Its rate constant (in s^(-1) ) at 600 K is "x" xx 10^(-6) . The value of x is ______ .(Nearest integer) [Given R=8.31 J K^(-1) "mol"^(-1) , log 6.36 xx 10^(-3)= -2.19, 10^(-4.79)= 1.62 xx10^(-5) ]
The rate constant k for the order gas phase decomposition of ethyl iodide, C_2H_5l rarrC_2H_4+Hl is 1.60xx10^(-5)s^(-1) ar 600 K and 6.36xx10^(-3)s^(-1) at 700 K. Calculate the energy of activation for this reaction.
For the water gas reaction, C(s) +H_(2)O(g) hArr CO(g)+H_(2)(g) the standard Gobbs free energy of reaction (at 1000K) is -8.1 kJ mol^(-1) . Calculate its equilibrium constant.
Using the Arrhenius equation : The rate constant fot the formation of hydrogen iodide from the elemewnts H_(2)(g)+I_(2)(g)rarr2HI(g) is 2.7xx10^(-4)L//(mol.s)at 600 k and 3.5xx10^(-3)L//(mol.s) at 650 k . (a) Find the activation energy E_(a) . (b) Calculate the rate constant at 700 k . Strategy : (a) Substitute the data given in the problem statement into the Equation (4.37) noted just before this example, then solve for E_(a) . , (b) Use the same equation, but substitute for k_(1), T_(1), T_(2) and E_(a) obtained in (a) and solve for k_(2) .
The decomposition of methyl iodid, 2CH_(3)I(g)rarrC_(2)H_(6)(g)+I_(2)(g) at 273^(@) C has a rate constant of 2.418xx10^(-5)s^(-1) . If activation energy for the reaction is +179.9 kJ "mol"^(-1) , what is the value of collision factor A at 273^(@)C ?
For the water gas reaction: C(s) +H_(2)O(g) hArr CO(g) +H_(2)(g) the standard Gibbs enegry for the reaction at 1000K is -8.1 kJ mol^(-1) . Calculate its equilibriu constant.
The decomposition of phosphine, 4PH_(3)(g) to P_(4)(g) + 6H_(2)(g) has rate law , Rate = k[PH_(3)] . The rate constant is 6.0 xx 10^(-4) s^(-1) at 300 K and activation energy is 3.05 xx 10^(5) J mol^(-1) . Calculate the value of the rate constant at 310 K ( R= 8.314 JK^(-1)mol^(-1))
For the water gas reaction C(s)+H_(2)O(g)hArrCO(g)+H_(2)(g) The standard Gibb's energy of energy of reaction (at 1000K) is -8.1KJmol^(-1) . Value of equilibrium constant is -