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The order of reaction is an experimental...

The order of reaction is an experimentally determined quanity. It may be zero, poistive, negative, or fractional. The kinetic equation of `nth` order reaction is
`k xx t = (1)/((n-1))[(1)/((a-x)^(n-1)) - (1)/(a^(n-1))]` …(i)
Half life of `nth` order reaction depends on the initial concentration according to the following relation:
`t_(1//2) prop (1)/(a^(n-1))` ...(ii)
The unit of the rate constant varies with the order but general relation for the unit of `nth` order reaction is
Units of `k = [(1)/(Conc)]^(n-1) xx "Time"^(-1)` ...(iii)
The differential rate law for `nth` order reaction may be given as:
`(dx)/(dt) = k[A]^(n)` ...(iv)
where `A` denotes the reactant.
In a chemical reaction `A rarr B`, it is found that the rate of the reaction doubles when the concentration of `A` is increased four times. The order of the reaction with respect to `A` is:

A

`0`

B

`(1)/(2)`

C

`1`

D

`2`

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To determine the order of the reaction with respect to reactant A, we can follow these steps: ### Step 1: Write the rate law expression The rate of a reaction can be expressed as: \[ \text{Rate} = k[A]^n \] where: - \( k \) is the rate constant, - \( [A] \) is the concentration of reactant A, - \( n \) is the order of the reaction with respect to A. ### Step 2: Set up the initial and changed conditions Let: - \( r_1 \) be the initial rate of the reaction when the concentration of A is \( [A]_1 \). - When the concentration of A is increased four times, it becomes \( [A]_2 = 4[A]_1 \). - The new rate of the reaction is \( r_2 = 2r_1 \) (the rate doubles). ### Step 3: Write the rate equations for both conditions For the initial condition: \[ r_1 = k[A]_1^n \] For the new condition: \[ r_2 = k[A]_2^n = k(4[A]_1)^n = k(4^n[A]_1^n) \] ### Step 4: Set up the equation based on the rate change Since \( r_2 = 2r_1 \), we can substitute the expressions for \( r_1 \) and \( r_2 \): \[ k(4^n[A]_1^n) = 2(k[A]_1^n) \] ### Step 5: Cancel out common terms We can cancel \( k \) and \( [A]_1^n \) from both sides (assuming \( [A]_1 \neq 0 \)): \[ 4^n = 2 \] ### Step 6: Solve for \( n \) To solve for \( n \), we can rewrite \( 4^n \) as \( (2^2)^n = 2^{2n} \): \[ 2^{2n} = 2^1 \] This implies: \[ 2n = 1 \] \[ n = \frac{1}{2} \] ### Conclusion The order of the reaction with respect to A is \( \frac{1}{2} \). ---

To determine the order of the reaction with respect to reactant A, we can follow these steps: ### Step 1: Write the rate law expression The rate of a reaction can be expressed as: \[ \text{Rate} = k[A]^n \] where: - \( k \) is the rate constant, - \( [A] \) is the concentration of reactant A, ...
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The order of reaction is an experimentally determined quanity. It may be zero, poistive, negative, or fractional. The kinetic equation of nth order reaction is k xx t = (1)/((n-1))[(1)/((a-x)^(n-1)) - (1)/(a^(n-1))] …(i) Half life of nth order reaction depends on the initial concentration according to the following relation: t_(1//2) prop (1)/(a^(n-1)) ...(ii) The unit of the rate constant varies with the order but general relation for the unit of nth order reaction is Units of k = [(1)/(Conc)]^(n-1) xx "Time"^(-1) ...(iii) The differential rate law for nth order reaction may be given as: (dX)/(dt) = k[A]^(n) ...(iv) where A denotes the reactant. The half life for a zero order reaction equals

The order of reaction is an experimentally determined quanity. It may be zero, poistive, negative, or fractional. The kinetic equation of nth order reaction is k xx t = (1)/((n-1))[(1)/((a-x)^(n-1)) - (1)/(a^(n-1))] …(i) Half life of nth order reaction depends on the initial concentration according to the following relation: t_(1//2) prop (1)/(a^(n-1)) ...(ii) The unit of the rate constant varies with the order but general relation for the unit of nth order reaction is Units of k = [(1)/(Conc)]^(n-1) xx "Time"^(-1) ...(iii) The differential rate law for nth order reaction may be given as: (dX)/(dt) = k[A]^(n) ...(iv) where A denotes the reactant. The unit of rate and rate constant are same for

The order of reaction is an experimentally determined quanity. It may be zero, poistive, negative, or fractional. The kinetic equation of nth order reaction is k xx t = (1)/((n-1))[(1)/((a-x)^(n-1)) - (1)/(a^(n-1))] …(i) Half life of nth order reaction depends on the initial concentration according to the following relation: t_(1//2) prop (1)/(a^(n-1)) ...(ii) The unit of the rate constant varies with the order but general relation for the unit of nth order reaction is Units of k = [(1)/(Conc)]^(n-1) xx "Time"^(-1) ...(iii) The differential rate law for nth order reaction may be given as: (dX)/(dt) = k[A]^(n) ...(iv) where A denotes the reactant. The rate constant for zero order reaction is where c_(0) and c_(t) are concentration of reactants at respective times.

The order of reaction is an experimentally determined quanity. It may be zero, poistive, negative, or fractional. The kinetic equation of nth order reaction is k xx t = (1)/((n-1))[(1)/((a-x)^(n-1)) - (1)/(a^(n-1))] …(i) Half life of nth order reaction depends on the initial concentration according to the following relation: t_(1//2) prop (1)/(a^(n-1)) ...(ii) The unit of the rate constant varies with the order but general relation for the unit of nth order reaction is Units of k = [(1)/(Conc)]^(n-1) xx "Time"^(-1) ...(iii) The differential rate law for nth order reaction may be given as: (dx)/(dt) = k[A]^(n) ...(iv) where A denotes the reactant. For a reaction: I^(ɵ) + OCl^(ɵ) rarr IO^(ɵ) + Cl^(ɵ) in an aqueous medium, the rate of the reaction is given by (d[IO^(ɵ)])/(dt) = k([I^(ɵ)][OCl^(ɵ)])/([overset(ɵ)(OH)]) The overall order of the reaction is

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