To solve the problem, we consider the first-order reaction \(\text{A(g)} \rightarrow 2\text{B(g)} + \text{C(g)}\) and apply the concept of partial pressures in relation to time and constant temperature. The given data involves the pressures at two different times: 200 torr after 23 seconds and 300 torr at completion (long time).
The reaction involves a change in total pressure due to decomposition, initially high with unreacted \( \text{A} \), dropping as the products form.
Let's denote the initial pressure of \( \text{A} \) as \( P_A^0 \). After the complete conversion of \( \text{A} \), the total pressure is 300 torr, thereby making the change in pressure due to reaction equal to \( 300-200=100 \, \text{torr} \) at 23 seconds similar:
\( P_A = P_A^0 - x \) where \( x \) is the change in \( A \). Now, since every mole of \( \text{A} \) gives rise to 3 moles of products, at completion:\[(1-x) \rightarrow (x) \]The total pressure increase due to \( x \) of \( A \) decomposing to give \( 3x \) is proportional to formation. Simplify:\[P_{total}=P_A^0 + 2x = 200\]and at time \(t\) (23s):\[200=(P_A^0 -x) + 3x\]thus at equilibrium pushing,[\(3x\)] we re-derive:
After substitution, equation implies using initial rate-integrated expression:\[k = \frac{2.303}{t} \log \left( \frac{P_\infty - P_0}{P_\infty - Pt} \right)\]
Given the pressures, it takes \(\log_{10}(2) = 0.301\), we substitute into the rate equation:
\[k = \frac{2.303}{23} \times \log \left( \frac{300-100}{300-200} \right)\]Evaluating with values:
\[k = \frac{2.303}{23} \times \log_{10}(2) \approx \frac{2.303}{23} \times 0.301\]
Approximating the result:
\[k \approx 0.301 \times 0.1 = 0.0303\]Thus, with the correct arithmetic:
\[k \approx 3 \times 10^{-2} \, \text{s}^{-1}\]
The reaction is: \[ \text{A(g)} \rightarrow 2\text{B(g)} + \text{C(g)} \]
Given:
\(P_{23} = P_0 + 2x = 200 \\ P_\infty = 3P_0 = 300 \\ P_0 = 100\)
The rate constant $K$ is calculated using:
\[ K = \frac{1}{t} \ln \frac{P_\infty - P_0}{P_\infty - P_t} \]
Substituting the values:
\[ K = \frac{2.3}{23} \log \frac{300 - 100}{300 - 200} \] \[ K = \frac{2.3 \times 0.301}{23} = 0.0301 = 3.01 \times 10^{-2} \, \text{s}^{-1} \]
The correct answer is (3).
What will be the equilibrium constant of the given reaction carried out in a \(5 \,L\) vessel and having equilibrium amounts of \(A_2\) and \(A\) as \(0.5\) mole and \(2 \times 10^{-6}\) mole respectively?
The reaction : \(A_2 \rightleftharpoons 2A\)

Cobalt chloride when dissolved in water forms pink colored complex $X$ which has octahedral geometry. This solution on treating with cone $HCl$ forms deep blue complex, $\underline{Y}$ which has a $\underline{Z}$ geometry $X, Y$ and $Z$, respectively, are
Consider the following data for the given reaction
\(2\)\(\text{HI}_{(g)}\) \(\rightarrow\) \(\text{H}_2{(g)}\)$ + $\(\text{I}_2{(g)}\)
The order of the reaction is __________.
What will be the equilibrium constant of the given reaction carried out in a \(5 \,L\) vessel and having equilibrium amounts of \(A_2\) and \(A\) as \(0.5\) mole and \(2 \times 10^{-6}\) mole respectively?
The reaction : \(A_2 \rightleftharpoons 2A\)
A black body is at a temperature of 2880 K. The energy of radiation emitted by this body with wavelength between 499 nm and 500 nm is U1, between 999 nm and 1000 nm is U2 and between 1499 nm and 1500 nm is U3. The Wien's constant, b = 2.88×106 nm-K. Then,