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Exercise · Q24

Q.A first order reaction has k=4.00×10−2 min−1k = 4.00\times 10^{-2}\ \text{min}^{-1}. Calculate the time taken for the concentration to fall

(a) from 0.80 mol L−10.80\ \text{mol L}^{-1} to 0.40 mol L−10.40\ \text{mol L}^{-1}, and
(b) from 0.40 mol L−10.40\ \text{mol L}^{-1} to 0.20 mol L−10.20\ \text{mol L}^{-1}. What do the two results show about the half-life of a first order reaction?
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(a) t=2.303klog⁡0.800.40=2.3030.0400log⁡2=57.575×0.3010=17.33 mint = \dfrac{2.303}{k}\log\dfrac{0.80}{0.40} = \dfrac{2.303}{0.0400}\log 2 = 57.575\times 0.3010 = 17.33\ \text{min}. (b) t=2.303klog⁡0.400.20=2.3030.0400log⁡2=17.33 mint = \dfrac{2.303}{k}\log\dfrac{0.40}{0.20} = \dfrac{2.303}{0.0400}\log 2 = 17.33\ \text{min} again, identical to (a). Both results also match t1/2=0.693/k=0.693/0.0400=17.325 mint_{1/2}=0.693/k = 0.693/0.0400 = 17.325\ \text{min} directly, since each interval is precisely one halving of concentration. The fact that the SAME time is needed to halve the concentration, whether starting from 0.80 mol L−10.80\ \text{mol L}^{-1} or from the already-lower 0.40 mol L−10.40\ \text{mol L}^{-1}, demonstrates directly that a first order reactio …

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