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Question: A first-order reaction \(({t_{\dfrac{1}{2}}} = 1day)\) completes \(x\% \) after 4 half-lives. Value ...

A first-order reaction (t12=1day)({t_{\dfrac{1}{2}}} = 1day) completes x%x\% after 4 half-lives. Value of xx is:
A. 87.587.5
B. 7575
C. 93.7593.75
D. 5050

Explanation

Solution

The half lifetime for 4 half-lives will be equal to 4 times the half-life of 1 half-life i.e. 1 day and substituting t12=4(1day)=4days{t_{\dfrac{1}{2}}}^\prime = 4(1day) = 4days in integrated rate equation for the first-order reaction, we can find the value of xx but first of all, we need to find the value of the rate constant kk. For a first-order reaction, k=2.303tlog10aaxk = \dfrac{{2.303}}{t}{\log _{10}}\dfrac{a}{{a - x}}
Here, aa is the initial concentration
xx is the amount of reactant reacting in time t

Complete step by step answer:
Now, we know that the half-life formula for the first-order reaction is,
t12=0.693k{t_{\dfrac{1}{2}}} = \dfrac{{0.693}}{k}
Here, kk is rate constant
For 1 half-life,
t12=1day{t_{\dfrac{1}{2}}} = 1day (Given)
\therefore For 4 half-lives,
t12=4(t12){t_{\dfrac{1}{2}}}^\prime = 4\left( {{t_{\dfrac{1}{2}}}} \right)
=4(1)= 4(1)
t12=4days{t_{\dfrac{1}{2}}}^\prime = 4days ……. (Equation number 1)
Now,
t12=0.693k{t_{\dfrac{1}{2}}} = \dfrac{{0.693}}{k}
So, k=0.693t12k = \dfrac{{0.693}}{{{t_{\dfrac{1}{2}}}}}
k=0.6931\Rightarrow k = \dfrac{{0.693}}{1}
k=0.693day1k = 0.693da{y^{ - 1}} ….. (Equation number 2)
For t=t12t = {t_{\dfrac{1}{2}}},
t12=2.303klog10aax{t_{\dfrac{1}{2}}} = \dfrac{{2.303}}{k}{\log _{10}}\dfrac{a}{{a - x}}
And for t=t12t = {t_{\dfrac{1}{2}}}^\prime ,
t12=2.303klog10100100x{t_{\dfrac{1}{2}}}^\prime = \dfrac{{2.303}}{k}{\log _{10}}\dfrac{{100}}{{100 - x}} …… (Equation number 3)
As the reaction completes x%x\% after 4 half-lives. (Given)
But t12=4days{t_{\dfrac{1}{2}}}^\prime = 4days …..(From Equation number 1)
And k=0.693day1k = 0.693da{y^{ - 1}} …..(From Equation number 2)
Substituting these values in Equation number 3,
4=2.3030.693log10100100x4 = \dfrac{{2.303}}{{0.693}}{\log _{10}}\dfrac{{100}}{{100 - x}}
4=3.3232[log10(100)log10(100x)]\Rightarrow 4 = 3.3232\left[ {{{\log }_{10}}\left( {100} \right) - {{\log }_{10}}\left( {100 - x} \right)} \right]
4=3.3232[2log10(100x)]\Rightarrow 4 = 3.3232\left[ {2 - {{\log }_{10}}\left( {100 - x} \right)} \right]
43.3232=2log10(100x)\Rightarrow \dfrac{4}{{3.3232}} = 2 - {\log _{10}}\left( {100 - x} \right)
1.2036=2log10(100x)\Rightarrow 1.2036 = 2 - {\log _{10}}\left( {100 - x} \right)
1.20362=log10(100x)\Rightarrow 1.2036 - 2 = - {\log _{10}}\left( {100 - x} \right)
0.7964=log10(100x)\Rightarrow - 0.7964 = - {\log _{10}}\left( {100 - x} \right)
0.7964=log10(100x)\Rightarrow 0.7964 = {\log _{10}}\left( {100 - x} \right)
Now, converting logarithmic form to exponential form,
100.7964=100x{10^{0.7964}} = 100 - x
Taking log on both the sides,
log(100.7964)=log(100x)\log \left( {{{10}^{0.7964}}} \right) = \log \left( {100 - x} \right)
0.7964=log10(100x)0.7964 = {\log _{10}}\left( {100 - x} \right)
Now taking antilog on both sides,
A.L.(0.7964)=A.L.[log10(100x)]A.L.\left( {0.7964} \right) = A.L.\left[ {{{\log }_{10}}\left( {100 - x} \right)} \right]
6.2574=100x6.2574 = 100 - x
6.2574100=x\Rightarrow 6.2574 - 100 = x
93.75=x\Rightarrow - 93.75 = - x
x=93.75x = 93.75
Hence, the value of xx is 93.7593.75

So, the correct answer is Option C.

Additional Information:
The concept of half-life was discovered by Ernest Rutherford in 1907. It relates to the time required by radioactive substances for disintegration or the formation of a new substance. It is also known as the half-life period.

Note: The rate constant of a second-order reaction is k=12atlogxaxk = \dfrac{1}{{2at}}\log \dfrac{x}{{a - x}}. The first-order rate constant depends on the concentration of only 1 among the reactants. We could see that the half-life of the first order is independent of the reactant concentration. The unit of the first-order reaction is sec1{\sec ^{ - 1}}. The unit of half-life is seconds.