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Step 1: Using First-Order Reaction Formula
The time required for the concentration to become \( \frac{1}{n} \) of its initial value in a first-order reaction is: \[ t_{1/n} = \frac{2.303}{k} \log n \] For \( t_{1/4} \): \[ t_{1/4} = \frac{2.303}{k} \log 4 = \frac{2.303}{k} (2 \times \log 2) \] Using \( \log 2 = 0.3 \), \[ t_{1/4} = \frac{2.303}{k} (2 \times 0.3) = \frac{2.303 \times 0.6}{k} \] For \( t_{1/10} \): \[ t_{1/10} = \frac{2.303}{k} \log 10 = \frac{2.303}{k} (1) \] Step 2: Calculating Ratio
\[ \frac{t_{1/4}}{t_{1/10}} = \frac{2.303 \times 0.6}{2.303 \times 1} = 0.6 \] \[ \frac{t_{1/4}}{t_{1/10}} \times 100 = 0.6 \times 100 = 60 \] Thus, the correct answer is 60.
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.
Observe the following data given in the table. (\(K_H\) = Henry's law constant)
Gas | CO₂ | Ar | HCHO | CH₄ |
---|---|---|---|---|
\(K_H\) (k bar at 298 K) | 1.67 | 40.3 | \(1.83 \times 10^{-5}\) | 0.413 |
The correct order of their solubility in water is