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The rate of reaction increases isgnifica...

The rate of reaction increases isgnificantly with increase in temperature. Generally, rate of reactions are doubled for every `10^(@)C` rise in temperature. Temperature coefficient gives us an idea about the change in the rate of a reaction for every `10^(@)C` change in temperature.
`"Temperature coefficient" (mu) = ("Rate constant of" (T + 10)^(@)C)/("Rate constant at" T^(@)C)`
Arrhenius gave an equation which describes aret constant `k` as a function of temperature
`k = Ae^(-E_(a)//RT)`
where `k` is the rate constant, `A` is the frequency factor or pre-exponential factor, `E_(a)` is the activation energy, `T` is the temperature in kelvin, `R` is the universal gas constant.
Equation when expressed in logarithmic form becomes
`log k = log A - (E_(a))/(2.303 RT)`
For which of the following reactions `k_(310)//k_(300)` would be maximum?

A

`P + Q rarr R, E_(a) = 10 kJ`

B

`E + F rarr D, E_(a) = 21 kJ`

C

`A + B rarr C, E_(a) = 10.5 kJ`

D

`L+M rarr N, E_(a) = 5 kJ`

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To solve the question regarding which reaction will have the maximum ratio of rate constants \( k_{310}/k_{300} \), we will use the Arrhenius equation and analyze the activation energies of the given reactions. ### Step-by-Step Solution: 1. **Understand the Arrhenius Equation**: The Arrhenius equation is given by: \[ k = A e^{-\frac{E_a}{RT}} \] where \( k \) is the rate constant, \( A \) is the frequency factor, \( E_a \) is the activation energy, \( R \) is the universal gas constant, and \( T \) is the temperature in Kelvin. 2. **Write the Rate Constants at Two Temperatures**: For two temperatures, \( T_1 = 300 \, K \) and \( T_2 = 310 \, K \): \[ k_{300} = A e^{-\frac{E_a}{R \cdot 300}} \] \[ k_{310} = A e^{-\frac{E_a}{R \cdot 310}} \] 3. **Calculate the Ratio \( \frac{k_{310}}{k_{300}} \)**: The ratio of the rate constants at these two temperatures can be expressed as: \[ \frac{k_{310}}{k_{300}} = \frac{A e^{-\frac{E_a}{R \cdot 310}}}{A e^{-\frac{E_a}{R \cdot 300}}} \] The \( A \) cancels out: \[ \frac{k_{310}}{k_{300}} = e^{-\frac{E_a}{R \cdot 310} + \frac{E_a}{R \cdot 300}} \] 4. **Simplify the Exponent**: This can be rewritten as: \[ \frac{k_{310}}{k_{300}} = e^{\frac{E_a}{R} \left( \frac{1}{300} - \frac{1}{310} \right)} \] 5. **Calculate the Difference**: The term \( \frac{1}{300} - \frac{1}{310} \) can be simplified: \[ \frac{1}{300} - \frac{1}{310} = \frac{310 - 300}{300 \times 310} = \frac{10}{93000} = \frac{1}{9300} \] 6. **Final Expression for the Ratio**: Thus, we have: \[ \frac{k_{310}}{k_{300}} = e^{\frac{E_a}{R \cdot 9300}} \] This shows that the ratio \( \frac{k_{310}}{k_{300}} \) is directly proportional to the activation energy \( E_a \). 7. **Conclusion**: To determine which reaction has the maximum ratio \( \frac{k_{310}}{k_{300}} \), we need to identify the reaction with the highest activation energy \( E_a \). According to the information given, the reaction with the highest activation energy is the second reaction with \( E_a = 21 \, \text{kJ/mol} \). ### Final Answer: The reaction for which \( \frac{k_{310}}{k_{300}} \) would be maximum is the second reaction with an activation energy of 21 kJ/mol. ---

To solve the question regarding which reaction will have the maximum ratio of rate constants \( k_{310}/k_{300} \), we will use the Arrhenius equation and analyze the activation energies of the given reactions. ### Step-by-Step Solution: 1. **Understand the Arrhenius Equation**: The Arrhenius equation is given by: \[ k = A e^{-\frac{E_a}{RT}} ...
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The rate of reaction increases isgnificantly with increase in temperature. Generally, rate of reactions are doubled for every 10^(@)C rise in temperature. Temperature coefficient gives us an idea about the change in the rate of a reaction for every 10^(@)C change in temperature. "Temperature coefficient" (mu) = ("Rate constant of" (T + 10)^(@)C)/("Rate constant at" T^(@)C) Arrhenius gave an equation which describes aret constant k as a function of temperature k = Ae^(-E_(a)//RT) where k is the rate constant, A is the frequency factor or pre-exponential factor, E_(a) is the activation energy, T is the temperature in kelvin, R is the universal gas constant. Equation when expressed in logarithmic form becomes log k = log A - (E_(a))/(2.303 RT) Activation energies of two reaction are E_(a) and E_(a)' with E_(a) gt E'_(a) . If the temperature of the reacting systems is increased form T_(1) to T_(2) ( k' is rate constant at higher temperature).

The rate of reaction increases isgnificantly with increase in temperature. Generally, rate of reactions are doubled for every 10^(@)C rise in temperature. Temperature coefficient gives us an idea about the change in the rate of a reaction for every 10^(@)C change in temperature. "Temperature coefficient" (mu) = ("Rate constant of" (T + 10)^(@)C)/("Rate constant at" T^(@)C) Arrhenius gave an equation which describes aret constant k as a function of temperature k = Ae^(-E_(a)//RT) where k is the rate constant, A is the frequency factor or pre-exponential factor, E_(a) is the activation energy, T is the temperature in kelvin, R is the universal gas constant. Equation when expressed in logarithmic form becomes log k = log A - (E_(a))/(2.303 RT) For a reaction E_(a) = 0 and k = 3.2 xx 10^(8)s^(-1) at 325 K . The value of k at 335 K would be

The rate of reaction increases isgnificantly with increase in temperature. Generally, rate of reactions are doubled for every 10^(@)C rise in temperature. Temperature coefficient gives us an idea about the change in the rate of a reaction for every 10^(@)C change in temperature. "Temperature coefficient" (mu) = ("Rate constant of" (T + 10)^(@)C)/("Rate constant at" T^(@)C) Arrhenius gave an equation which describes aret constant k as a function of temperature k = Ae^(-E_(a)//RT) where k is the rate constant, A is the frequency factor or pre-exponential factor, E_(a) is the activation energy, T is the temperature in kelvin, R is the universal gas constant. Equation when expressed in logarithmic form becomes log k = log A - (E_(a))/(2.303 RT) For the given reactions, following data is given {:(PrarrQ,,,,k_(1) =10^(15)exp((-2000)/(T))),(CrarrD,,,,k_(2) = 10^(14)exp((-1000)/(T))):} Temperature at which k_(1) = k_(2) is

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