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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.
The rate constant for zero order reaction is
where `c_(0)` and `c_(t)` are concentration of reactants at respective times.

A

`k = (c_(0))/(2t)`

B

`k = (c_(0)-c_(t))/(t)`

C

`k = ln.(c_(0)-c_(t))/(2t)`

D

`k = (c_(0))/(c_(t))`

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To determine the rate constant for a zero-order reaction, we can follow these steps: ### Step-by-Step Solution: 1. **Understanding Zero-Order Reactions**: In a zero-order reaction, the rate of reaction is constant and does not depend on the concentration of the reactants. The rate law can be expressed as: \[ \frac{dX}{dt} = -k \] where \( k \) is the rate constant. 2. **Setting Up the Differential Equation**: Rearranging the rate law gives: \[ -dX = k \, dt \] 3. **Integrating Both Sides**: We integrate both sides to find the relationship between concentration and time. The limits for concentration will be from \( C_0 \) (initial concentration) to \( C_t \) (concentration at time \( t \)), and the limits for time will be from \( 0 \) to \( t \): \[ \int_{C_0}^{C_t} -dX = \int_{0}^{t} k \, dt \] 4. **Performing the Integration**: The left side integrates to: \[ -(C_t - C_0) = -\Delta C \] The right side integrates to: \[ kt \] Therefore, we have: \[ C_0 - C_t = kt \] 5. **Rearranging for Rate Constant \( k \)**: Rearranging the equation gives us the expression for the rate constant: \[ k = \frac{C_0 - C_t}{t} \] 6. **Conclusion**: The rate constant \( k \) for a zero-order reaction is given by: \[ k = \frac{C_0 - C_t}{t} \] This means that the rate constant is directly proportional to the change in concentration over time.

To determine the rate constant for a zero-order reaction, we can follow these steps: ### Step-by-Step Solution: 1. **Understanding Zero-Order Reactions**: In a zero-order reaction, the rate of reaction is constant and does not depend on the concentration of the reactants. The rate law can be expressed as: \[ \frac{dX}{dt} = -k ...
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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. 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:

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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