A brief note on Integrated Rate Equations and Half-Life . Read it before a test. Try each question at the end before you open its answer.
Zero order Rate law: rate = k = k = k . The unit of k k k is mol L − 1 time − 1 \text{mol L}^{-1}\,\text{time}^{-1} mol L − 1 time − 1 . Integrated equation: [ R ] = [ R ] 0 − k t [R] = [R]_0 - kt [ R ] = [ R ] 0 − k t . A graph of [ R ] [R] [ R ] against t t t is a straight line with slope − k -k − k . Half-life: t 1 / 2 = [ R ] 0 2 k t_{1/2} = \dfrac{[R]_0}{2k} t 1/2 = 2 k [ R ] 0 . It is proportional to the start concentration. End of the reaction: t = [ R ] 0 k t = \dfrac{[R]_0}{k} t = k [ R ] 0 , which is 2 t 1 / 2 2t_{1/2} 2 t 1/2 . Where it happens: when a surface, an enzyme or the light limits the speed. First order Rate law: rate = k [ R ] = k[R] = k [ R ] . The unit of k k k is time − 1 \text{time}^{-1} time − 1 . Integrated equation: ln [ R ] = ln [ R ] 0 − k t \ln[R] = \ln[R]_0 - kt ln [ R ] = ln [ R ] 0 − k t , or [ R ] = [ R ] 0 e − k t [R] = [R]_0e^{-kt} [ R ] = [ R ] 0 e − k t . Rate constant: k = 2.303 t log [ R ] 0 [ R ] k = \dfrac{2.303}{t}\log\dfrac{[R]_0}{[R]} k = t 2.303 log [ R ] [ R ] 0 . Graph: ln [ R ] \ln[R] ln [ R ] against t t t is a straight line with slope − k -k − k . A log [ R ] \log[R] log [ R ] graph has slope − k / 2.303 -k/2.303 − k /2.303 . Gas reaction, one gas giving two: k = 2.303 t log p i 2 p i − p t k = \dfrac{2.303}{t}\log\dfrac{p_i}{2p_i - p_t} k = t 2.303 log 2 p i − p t p i . Half-life and fractions First order: t 1 / 2 = 0.693 k t_{1/2} = \dfrac{0.693}{k} t 1/2 = k 0.693 . It is the same at every stage and for every start concentration. Fraction left: ( 1 2 ) n \left(\tfrac{1}{2}\right)^n ( 2 1 ) n after n = t / t 1 / 2 n = t/t_{1/2} n = t / t 1/2 half-lives. Any fraction reacted, f f f : t = 2.303 k log 1 1 − f t = \dfrac{2.303}{k}\log\dfrac{1}{1-f} t = k 2.303 log 1 − f 1 . About ten half-lives take a first order reaction to 99.9 %. Reading the order: the half-life is proportional to [ R ] 0 [R]_0 [ R ] 0 for zero order, constant for first order, and proportional to 1 / [ R ] 0 1/[R]_0 1/ [ R ] 0 for second order. Radioactive decay follows the first order law. Pseudo first order Meaning: one reactant is in large excess, so its concentration hardly changes. Constant: k ′ = k [ B ] 0 k' = k[\text{B}]_0 k ′ = k [ B ] 0 , with the unit s − 1 \text{s}^{-1} s − 1 . The true rate constant is k = k ′ / [ B ] 0 k = k'/[\text{B}]_0 k = k ′ / [ B ] 0 . Test: change the excess, and k ′ k' k ′ changes in the same ratio. Examples: sucrose in dilute acid with water as the excess, and a dye fading in an excess of alkali. A worked example A first order reaction has k = 0.0173 min − 1 k = 0.0173\ \text{min}^{-1} k = 0.0173 min − 1 and starts at 0.56 mol/L 0.56\ \text{mol/L} 0.56 mol/L . Find the half-life, the concentration after 100 min 100\ \text{min} 100 min and the time for 75 % to react.
Half-life. t 1 / 2 = 0.693 0.0173 min − 1 = 40.1 min t_{1/2} = \dfrac{0.693}{0.0173\ \text{min}^{-1}} = 40.1\ \text{min} t 1/2 = 0.0173 min − 1 0.693 = 40.1 min . After 100 min 100\ \text{min} 100 min . k t = 0.0173 min − 1 × 100 min = 1.73 kt = 0.0173\ \text{min}^{-1} \times 100\ \text{min} = 1.73 k t = 0.0173 min − 1 × 100 min = 1.73 . Then [ R ] = 0.56 mol/L × e − 1.73 = 0.0993 mol/L [R] = 0.56\ \text{mol/L} \times e^{-1.73} = 0.0993\ \text{mol/L} [ R ] = 0.56 mol/L × e − 1.73 = 0.0993 mol/L . For 75 %. This is two half-lives, so 2 × 40.1 min = 80.2 min 2 \times 40.1\ \text{min} = 80.2\ \text{min} 2 × 40.1 min = 80.2 min . Practice with new numbers
A program to try The program checks which graph is straight for a set of readings. A straight ln [ R ] \ln[R] ln [ R ] graph means first order.
Run it. Which graph misses its straight line by less, [ R ] [R] [ R ] or ln [ R ] \ln[R] ln [ R ] ? What order does that point to?
1. Change the readings to 0.80, 0.70, 0.60, 0.50, 0.40. Which graph is straight now?
Mistakes to avoid Forgetting 2.303 when you use log \log log instead of ln \ln ln . Turning 0.693 k \dfrac{0.693}{k} k 0.693 upside down. A bigger k k k gives a shorter half-life. Using the total pressure as the pressure of the reactant in a gas reaction. Using a zero order equation after the reactant is gone. It holds only up to t = [ R ] 0 / k t = [R]_0/k t = [ R ] 0 / k . Calling k ′ k' k ′ the true rate constant of a pseudo first order reaction. Check yourself Which order has a half-life that does not depend on the start concentration? Stuck? Show a hint Show the answerAbout how many half-lives does a first order reaction need to be 99.9 % complete? Stuck? Show a hint Show the answerA zero order reaction starts at 0.40 mol/L 0.40\ \text{mol/L} 0.40 mol/L and has k = 0.020 mol L − 1 min − 1 k = 0.020\ \text{mol L}^{-1}\,\text{min}^{-1} k = 0.020 mol L − 1 min − 1 . When is the reactant all used up? Stuck? Show a hint Show the answerHow do you find k k k from a straight-line graph of ln [ R ] \ln[R] ln [ R ] against t t t ? Stuck? Show a hint Show the answer