The integrated rate equation for a first-order reaction is \(\frac{kt}{2.303} = logR_o – logR_t\). The straight line graph is obtained by plotting: |
time vs \(R_t\) time vs \(log R_t\) time vs \(\frac{1}{R_t}\) time vs\(R_o\) |
time vs \(log R_t\) |
The correct answer is option 2. time vs \(log R_t\). We have the integrated rate equation for a first-order reaction: \(\frac{kt}{2.303} = \log\frac{R_0}{R_t}\) Where: \(k\) is the rate constant for the reaction. \(t\) is time. \(R_0\) is the initial concentration of the reactant. \(R_t\) is the concentration of the reactant at time \(t\). Now, to obtain a straight-line graph, we need to manipulate this equation into the form \(y = mx + c\), where \(y\) is the dependent variable, \(x\) is the independent variable, \(m\) is the slope, and \(b\) is the y-intercept. First, let's isolate the logarithmic term on one side: \(log R_t = -\frac{k}{2.303}t + log R_o\) This equation is comparable to equation of a straight line \((y = mx + c)\).When a graph is plotted between \(log R_t \)and time \(t\) at different intervals of time we get a straight line. |