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For the following reaction scheme (homogeneous), the rate constant has units : \(A + B \overset{k}{\rightarrow} C\)
The first order rate constant for a certain reaction increases from 1.667 × 10-6 s-1 at 727ºC to 1.667 × 10-4 s-1 at 1571 ºC.The rate constant at 1150ºC, assuming constancy of activation energy over the given temperature range is[Given : log 19.9 = 1.299]
Velocity constant K of are action is affected by
Velocity constant ‘K’ is characteristic constant of are action and depends only on temperature and catalyst.
T50 of first -order reaction is 10 min. Starting with 10 mol L-1,rate after 20 minis
The rate constant for the reaction 2N2O5 ⟶ 4NO2 + O2 is 3.10 ×10-5 sec–1. If the rate is 2.4 ×10-5 mol litre-1 sec-1 then the concentration of N2O5 (in mol litre-1) is :
In a first order reaction the concentration of reactant decreases from 800 mol/dm3 to 50 mol/dm3 in 2 × 104 sec.The rate constant of reaction in sec-1 is:
For a first order reaction, to obtain a positive slope, we need to plot {where [A] is the concentration of reactant A}
For a first order reaction the positive slope is obtained when we plot – loge[A] vs t.
For the reaction 2N2O5 ⟶ 4NO2 + O2,rate and rate constant are 1.02× 10-4 mol lit-1sec-1 and 3.4 × 10-5 sec-1 respectively then concentration of N2O5 at that time will be
From data 1 and 3, it is clear that keeping (B) const, [A] is doubled, rate remains unaffected. Hence rate is independent of [A]. From 1 and 4, keeping [A] constant,[B] is doubled, rate become 8 times. Hence rate ∝ [B]3