Given that the rate of a first-order reaction is decreasing over time, we can use the integrated rate law for first-order kinetics:
Rate = \( k[A]_0 e^{-kt} \)
At time \( t = 10 \) min:
0.04 = \( k[A]_0 e^{-k \times 600} \)
At time \( t = 20 \) min:
0.03 = \( k[A]_0 e^{-k \times 1200} \)
Dividing equation (2) by equation (1):
\( \frac{0.03}{0.04} = e^{-k \times (1200 - 600)} \)
\( \frac{4}{3} = e^{-600k} \)
Taking natural log:
\( \ln \left( \frac{4}{3} \right) = 600k \)
Now solve for \( t_{\frac{1}{2}} \) using:
\( t_{\frac{1}{2}} = \frac{\ln 2}{k} \)
\( t_{\frac{1}{2}} = \frac{600 \ln 2}{\ln \left( \frac{4}{3} \right)} \) sec.
Now using the given values:
\( t_{\frac{1}{2}} = 600 \times \frac{\log 2}{\log 4 - \log 3} = 10 \times \frac{0.3010}{0.6020 - 0.4771} \) min
\( t_{\frac{1}{2}} = 24.08 \) min
\( t_{\frac{1}{2}} = 24 \)
The problem asks for the half-life of a first-order reaction, given the reaction rates at two different times.
For a first-order reaction, the rate of reaction is directly proportional to the concentration of the reactant at that instant. Let the reaction be \( A \rightarrow \text{Products} \).
The rate law is given by:
\[ \text{Rate} = k[A] \]
where \(k\) is the rate constant and \([A]\) is the concentration of the reactant.
The integrated rate law for a first-order reaction is:
\[ k = \frac{2.303}{t_2 - t_1} \log_{10}\left(\frac{[A_1]}{[A_2]}\right) \]
where \([A_1]\) and \([A_2]\) are the concentrations of the reactant at times \(t_1\) and \(t_2\), respectively.
Since the rate is directly proportional to the concentration (\(\text{Rate} \propto [A]\)), we can substitute the rates in place of the concentrations in the integrated rate law:
\[ k = \frac{2.303}{t_2 - t_1} \log_{10}\left(\frac{\text{Rate}_1}{\text{Rate}_2}\right) \]
The half-life (\(t_{1/2}\)) of a first-order reaction is related to the rate constant \(k\) by the formula:
\[ t_{1/2} = \frac{0.693}{k} = \frac{2.303 \log_{10}(2)}{k} \]
Step 1: List the given information.
Step 2: Calculate the rate constant (\(k\)) of the reaction.
We use the integrated rate law expressed in terms of rates. The time interval is \(t_2 - t_1 = 20 - 10 = 10\) minutes.
\[ k = \frac{2.303}{10} \log_{10}\left(\frac{0.04}{0.03}\right) \] \[ k = \frac{2.303}{10} \log_{10}\left(\frac{4}{3}\right) \]
Using the logarithm property \(\log(\frac{a}{b}) = \log(a) - \log(b)\):
\[ k = \frac{2.303}{10} (\log_{10}(4) - \log_{10}(3)) \]
Using the property \(\log(a^n) = n\log(a)\):
\[ k = \frac{2.303}{10} (2\log_{10}(2) - \log_{10}(3)) \]
Substitute the given values for \(\log(2)\) and \(\log(3)\):
\[ k = \frac{2.303}{10} (2 \times 0.3010 - 0.4771) \] \[ k = \frac{2.303}{10} (0.6020 - 0.4771) \] \[ k = \frac{2.303}{10} (0.1249) \] \[ k \approx 0.02877 \, \text{min}^{-1} \]
The unit of the rate constant is min-1 because the time interval used was in minutes.
Step 3: Calculate the half-life (\(t_{1/2}\)) of the reaction.
Using the formula for the half-life of a first-order reaction:
\[ t_{1/2} = \frac{0.693}{k} \]
Alternatively, to avoid intermediate calculations and potential rounding errors, we can use the expression involving logarithms:
\[ t_{1/2} = \frac{2.303 \log_{10}(2)}{k} = \frac{2.303 \log_{10}(2)}{\frac{2.303}{10} (\log_{10}(4/3))} \]
The \(2.303\) terms cancel out:
\[ t_{1/2} = \frac{10 \log_{10}(2)}{\log_{10}(4/3)} \]
Substitute the log values into the simplified expression:
\[ t_{1/2} = \frac{10 \times 0.3010}{2\log_{10}(2) - \log_{10}(3)} \] \[ t_{1/2} = \frac{3.010}{2 \times 0.3010 - 0.4771} \] \[ t_{1/2} = \frac{3.010}{0.6020 - 0.4771} \] \[ t_{1/2} = \frac{3.010}{0.1249} \] \[ t_{1/2} \approx 24.099 \, \text{minutes} \]
Rounding to the nearest significant figures, the half-life is approximately 24.1 minutes.
The half-life of the reaction is 24.1 minutes.
For the reaction \( A + B \to C \), the rate law is found to be \( \text{rate} = k[A]^2[B] \). If the concentration of \( A \) is doubled and \( B \) is halved, by what factor does the rate change?

Nature of compounds TeO₂ and TeH₂ is___________ and ______________respectively.