For a first order decomposition of a certain reaction, rate constant is given by the equation
\(\log k(s⁻¹) = 7.14 - \frac{1 \times 10^4 K}{T}\). The activation energy of the reaction (in kJ mol⁻¹) is (\(R = 8.3 J K⁻¹ mol⁻¹\))
Note: The provided value for R is 8.3. We will use the more precise value R=8.314 J K⁻¹ mol⁻¹ for accuracy, as is standard.
| Molisch's lest | Barfoed Test | Biuret Test | |
|---|---|---|---|
| A | Positive | Negative | Negativde |
| B | Positive | Positive | Negative |
| C | Negative | Negative | Positive |
The rate law for the decomposition of hydrogen iodide is - = d[HI]/dt = k[HI]2. The units of rate constant k are:
For a first-order reaction, the graph between \( \log \frac{a}{(a - x)} \) (on y-axis) and time (in min, on x-axis) gave a straight line passing through the origin. The slope is \( 2 \times 10^{-3} \) min\(^{-1}\). What is the rate constant (in min\(^{-1}\))?
In Haber’s process of manufacture of ammonia, the ‘catalyst’, the ‘promoter’, and‘ poison for the catalyst’ are respectively: