Home
Class 12
CHEMISTRY
A reactant (A) forms two products A ov...

A reactant `(A)` forms two products
`A overset (k_(1))rarr B`, Activation energy `E_(a1)`
`A overset (k_(2))rarr C`, Activation energy `E_(a2)`
If `E_(a_(2)) = 2E_(a_(1))` then `k_(1)` and `k_(2)` are related as

A

Reaction 2 is slow compared to reaction 1

B

Reaction 2 is more exothermic than reaction 1

C

Reaction 2 is more endothermic than reaction 1

D

Reaction 2 is fast compared to reaction 1

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we will use the Arrhenius equation, which relates the rate constants of reactions to their activation energies. The Arrhenius equation is given by: \[ k = A e^{-\frac{E_a}{RT}} \] where: - \( k \) is the rate constant, - \( A \) is the pre-exponential factor, - \( E_a \) is the activation energy, - \( R \) is the universal gas constant, - \( T \) is the temperature in Kelvin. ### Step 1: Write the Arrhenius equation for both reactions For the reaction \( A \overset{k_1}{\rightarrow} B \): \[ k_1 = A e^{-\frac{E_{a1}}{RT}} \quad \text{(1)} \] For the reaction \( A \overset{k_2}{\rightarrow} C \): \[ k_2 = A e^{-\frac{E_{a2}}{RT}} \quad \text{(2)} \] ### Step 2: Divide the two equations Now, we will divide equation (1) by equation (2): \[ \frac{k_1}{k_2} = \frac{A e^{-\frac{E_{a1}}{RT}}}{A e^{-\frac{E_{a2}}{RT}}} \] The \( A \) terms cancel out: \[ \frac{k_1}{k_2} = e^{-\frac{E_{a1}}{RT}} \cdot e^{\frac{E_{a2}}{RT}} \] ### Step 3: Simplify the exponent Using the property of exponents that states \( e^a \cdot e^b = e^{a+b} \): \[ \frac{k_1}{k_2} = e^{-\frac{E_{a1}}{RT} + \frac{E_{a2}}{RT}} = e^{\frac{E_{a2} - E_{a1}}{RT}} \] ### Step 4: Substitute the relationship between activation energies Given that \( E_{a2} = 2E_{a1} \), we substitute this into the equation: \[ \frac{k_1}{k_2} = e^{\frac{2E_{a1} - E_{a1}}{RT}} = e^{\frac{E_{a1}}{RT}} \] ### Step 5: Rearranging the equation Now, we can express \( k_1 \) in terms of \( k_2 \): \[ k_1 = k_2 e^{\frac{E_{a1}}{RT}} \] ### Conclusion Thus, the relationship between \( k_1 \) and \( k_2 \) is: \[ k_1 = k_2 e^{\frac{E_{a1}}{RT}} \]

To solve the problem, we will use the Arrhenius equation, which relates the rate constants of reactions to their activation energies. The Arrhenius equation is given by: \[ k = A e^{-\frac{E_a}{RT}} \] where: - \( k \) is the rate constant, ...
Promotional Banner

Topper's Solved these Questions

  • CHEMICAL KINETICS

    VMC MODULES ENGLISH|Exercise Level-2 ( Numerical Value Type for JEE Main )|15 Videos
  • CHEMICAL KINETICS

    VMC MODULES ENGLISH|Exercise JEE Main (Archive)|56 Videos
  • CHEMICAL KINETICS

    VMC MODULES ENGLISH|Exercise Level-1|75 Videos
  • CHEMICAL EQUILIBRIUM

    VMC MODULES ENGLISH|Exercise IN-CHAPTER EXERCISE - G|10 Videos
  • CHEMICAL THERMODYNAMICS

    VMC MODULES ENGLISH|Exercise IN - CHAPTER EXERCISE - L|10 Videos

Similar Questions

Explore conceptually related problems

Activation energy (E_(a)) and rate constants ( k_(1) and k_(2) ) of a chemical reaction at two different temperatures ( T_(1) and T_(2) ) are related by

Why is K_(a_(2)) ltlt K_(a_(1)) for H_(2) SO_(4) in water ?

Mechanism of the reaction is: A overset(k_(1))rarrB, 2Aoverset(k_(2))rarr C + D What is (-d[A])/(dt) ?

A colliison between reactant molecules must occur with a certain minimum energy before it is effective in yielding Product molecules. This minimum energy is called activation energy E_(a) Large the value of activation energy, smaller the value of rate constant k . Larger is the value of activation energy, greater is the effect of temperature rise on rate constant k . E_(f) = Activation energy of forward reaction E_(b) = Activation energy of backward reaction Delta H = E_(f) - E_(b) E_(f) = threshold energy For two reactions, activation energies are E_(a1) and E_(a2) , rate constant are k_(1) and k_(2) at the same temperature. If k_(1) gt k_(2) , then

Two reaction : X rarr Products and Y rarr Products have rate constants k_(1) and k_(2) at temperature T and activation energies E_(1) and E_(2) , respectively. If k_(1) gt k_(2) and E_(1) lt E_(2) (assuming that the Arrhenius factor is same for both the Products), then (I) On increaisng the temperature, increase in k_(2) will be greater than increaisng in k_(1) . (II) On increaisng the temperature, increase in k_(1) will be greater than increase in k_(2) . (III) At higher temperature, k_(1) will be closer to k_(2) . (IV) At lower temperature, k_(1) lt k_(2)

Mechanism of the reaction is: A_(2) overset(k_(2))hArr 2A A + B overset(k_(2))rarr C A_(2) + C overset(k)rarr D + A What is (d[D])/(dt) ?

Mechanism of the reaction is: A_(2) underset(k')overset(k)hArr 2A A + B_(2) overset(k_(2))rarr C + B B + A_(2) overset(k_(2))rarr C + A What is (-d[A_(2)])/(dt)

A colliison between reactant molecules must occur with a certain minimum energy before it is effective in yielding Product molecules. This minimum energy is called activation energy E_(a) Large the value of activation energy, smaller the value of rate constant k . Larger is the value of activation energy, greater is the effect of temperature rise on rate constant k . E_(f) = Activation energy of forward reaction E_(b) = Activation energy of backward reaction Delta H = E_(f) - E_(b) E_(f) = threshold energy If a reaction A + B rarr C is exothermic to the extent 30 kJ mol^(-1) and the forward reaction has an activation energy of 249 kJ mol^(-1) the activation energy for reverse reaction in kJ mol^(-1) is

A colliison between reactant molecules must occur with a certain minimum energy before it is effective in yielding Product molecules. This minimum energy is called activation energy E_(a) Large the value of activation energy, smaller the value of rate constant k . Larger is the value of activation energy, greater is the effect of temperature rise on rate constant k . E_(f) = Activation energy of forward reaction E_(b) = Activation energy of backward reaction Delta H = E_(f) - E_(b) E_(f) = threshold energy The rate constant of a certain reaction is given by k = Ae^(-E_(a)//RT) (where A = Arrhenius constant). Which factor should be lowered so that the rate of reaction may increase?

A colliison between reactant molecules must occur with a certain minimum energy before it is effective in yielding Product molecules. This minimum energy is called activation energy E_(a) Large the value of activation energy, smaller the value of rate constant k . Larger is the value of activation energy, greater is the effect of temperature rise on rate constant k . E_(f) = Activation energy of forward reaction E_(b) = Activation energy of backward reaction Delta H = E_(f) - E_(b) E_(f) = threshold energy For the following reaction at a particular temperature, according to the equations 2N_(2)O_(5) rarr 4NO_(2)+O_(2) 2NO_(2) + (1)/(2)O_(2) rarr N_(2)O_(5) The activation energies are E_(1) and E_(2) , respectively. Then

VMC MODULES ENGLISH-CHEMICAL KINETICS -Level-2
  1. If a homogeneous catalytic reaction follows three alternative paths A,...

    Text Solution

    |

  2. Two different first order reactions have rate consants k(1) and k(2) "...

    Text Solution

    |

  3. Consider the following statement : 1 The rate of reaction is always ...

    Text Solution

    |

  4. In the reaction A+BrarrC+D, the rate ((dx)/(dt)) when plotted against ...

    Text Solution

    |

  5. Initial concentration of reactant for nth order reaction is 'a'. Which...

    Text Solution

    |

  6. According to collision theory, which of the following is the criteria ...

    Text Solution

    |

  7. For the first-order reaction (C=C(0)e^(-k(1)^(t))) and T(av)=k(1)^(-1)...

    Text Solution

    |

  8. A reactant (A) forms two products A overset (k(1))rarr B, Activation...

    Text Solution

    |

  9. Consider the reaction : 2H(2)(g)+2NO(g)rarrN(2)(g)+2H(2)(g) The r...

    Text Solution

    |

  10. Which of the following is correct?

    Text Solution

    |

  11. Consider the following reaction. The reaction is first order in each ...

    Text Solution

    |

  12. If -((dN)/(dt))(o) is the initial activity and -((dN)/(dt)) is the act...

    Text Solution

    |

  13. For the second order reaction, concentration (x) of the product at tim...

    Text Solution

    |

  14. Consider following two competing first ordr reactions, Poverset(k(1)...

    Text Solution

    |

  15. Which of the following is pseudo-unimolecular reaction ?

    Text Solution

    |

  16. If the rate law is -(d[A])/(dt) =k[A] State I, at t = 0 state I...

    Text Solution

    |

  17. For the following reaction, A overset(500 K)rarr Products A overse...

    Text Solution

    |

  18. Following reaction can take place in both direction A {:(k(1)),(k(2)):...

    Text Solution

    |

  19. The rate constant for the reaction in gaseous phase O+O(3) rarr 2O(2...

    Text Solution

    |

  20. The rate constant in numerically the same for the theee reaction of fi...

    Text Solution

    |