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Question: The isotopes \({U^{238}}\) and \({U^{235}}\) occur in nature in the ratio \(140:1\). Assuming that a...

The isotopes U238{U^{238}} and U235{U^{235}} occur in nature in the ratio 140:1140:1. Assuming that at the time of earth formation, they were present in equal ratio, the estimated age of earth will be:
(The half-life period of U238{U^{238}} and U235{U^{235}} are 4.5×1094.5 \times {10^9} and 7.13×1087.13 \times {10^8} years, respectively.)
A. 6.04×1096.04 \times {10^9} years
B. 6.25×1096.25 \times {10^9} years
C. 6.59×1096.59 \times {10^9} years
D. none of these

Explanation

Solution

The decomposition of uranium follows first order kinetics. To answer this question, you should recall the formula for decrease in the concentration of reactants in a first order reaction with time.
Formula used:
Ct=C0ekt{C_t} = {C_0}{e^{ - kt}} …..(1.1)
For first order reaction, k=ln2Tk = \dfrac{{\ln 2}}{T} …..(1.2)
Where, Ct{C_t}is concentration of reactant at time tt, C0{C_0} is initial concentration of reactant, tt is time, kk is rate constant and TT is half-life of the reactant.

Complete step by step answer:
We are given the question that initial concentrations of U238{U^{238}} and U235{U^{235}} are equal.
Let the initial concentrations of U238{U^{238}} and U235{U^{235}} be C0{C_0} and final concentrations of U238{U^{238}} and U235{U^{235}} at time tt be C1{C_1} and C2{C_2} respectively.
We know that Ct=C0ekt{C_t} = {C_0}{e^{ - kt}}.
Hence,
C1=C0ek1t\Rightarrow {C_1} = {C_0}{e^{ - {k_1}t}} …..(1.3)
C2=C0ek2t\Rightarrow {C_2} = {C_0}{e^{ - {k_2}t}} …..(1.4)
where k1{k_1} and k2{k_2} are the rate constants for the decomposition of U238{U^{238}} and U235{U^{235}} respectively.
We know that, C1C2=1401\dfrac{{{C_1}}}{{{C_2}}} = \dfrac{{140}}{1} …..(1.5)
Dividing equation (1.3) by equation (1.4), we get,
C1C2=C0ek1tC0ek2t=ek1tek2t C1C2=ek2tk1t  \dfrac{{{C_1}}}{{{C_2}}} = \dfrac{{{C_0}{e^{ - {k_1}t}}}}{{{C_0}{e^{ - {k_2}t}}}} = \dfrac{{{e^{ - {k_1}t}}}}{{{e^{ - {k_2}t}}}} \\\ \Rightarrow \dfrac{{{C_1}}}{{{C_2}}} = {e^{{k_2}t - {k_1}t}} \\\
Taking natural log on both sides of the equation, we get
(k2k1)t=ln(C1C2)\left( {{k_2} - {k_1}} \right)t = \ln \left( {\dfrac{{{C_1}}}{{{C_2}}}} \right)
Rearranging to get tt,
t=ln(C1C2)(k2k1)t = \dfrac{{\ln \left( {\dfrac{{{C_1}}}{{{C_2}}}} \right)}}{{\left( {{k_2} - {k_1}} \right)}} ……(1.6)
From equation (1.2), we know that,
k1=ln2T1{k_1} = \dfrac{{\ln 2}}{{{T_1}}} and k2=ln2T2{k_2} = \dfrac{{\ln 2}}{{{T_2}}}, where T1=4.5×109years{T_1} = 4.5 \times {10^9}yearsand T2=7.13×108years{T_2} = 7.13 \times {10^8}years are half-lives of U238{U^{238}}and U235{U^{235}}respectively.
Substituting these values in equation (1.6), We get,
t=log(140)log2[T1×T2T1T2]\Rightarrow t = \dfrac{{\log \left( {140} \right)}}{{\log 2}}\left[ {\dfrac{{{T_1} \times {T_2}}}{{{T_1} - {T_2}}}} \right] t=ln(C1C2)ln2(1T11T2)=log(140)log2(T1T2T1.T2)t = \dfrac{{\ln \left( {\dfrac{{{C_1}}}{{{C_2}}}} \right)}}{{\ln 2\left( {\dfrac{1}{{{T_1}}} - \dfrac{1}{{{T_2}}}} \right)}} = \dfrac{{\log \left( {140} \right)}}{{\log 2\left( {\dfrac{{{T_1} - {T_2}}}{{{T_1}.{T_2}}}} \right)}}
t=log(140)log2[T1×T2T1T2]\Rightarrow t = \dfrac{{\log \left( {140} \right)}}{{\log 2}}\left[ {\dfrac{{{T_1} \times {T_2}}}{{{T_1} - {T_2}}}} \right]
t=2.14610.3010[4.5×109×7.13×1084.5×1097.13×108]\Rightarrow t = \dfrac{{2.1461}}{{0.3010}}\left[ {\dfrac{{4.5 \times {{10}^9} \times 7.13 \times {{10}^8}}}{{4.5 \times {{10}^9} - 7.13 \times {{10}^8}}}} \right]
t=6.04×109years\therefore t = 6.04 \times {10^9}years

Hence, the correct option is A.

Note:
For a first order reaction, half-life is independent of the initial concentration of the reactant. The concentration of reactant decreases exponentially with time in a first order equation. If we are given the value of C0{C_0} and Ct{C_t} at different time instants, the value of kk can be calculated for different time instants by using the first order law. If the reaction for which the data is given is a first order reaction, then all values of kk will be approximately equal to each other.