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Chapter 3 Β· Chemical Kinetics

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#1 SUB 4M πŸ–Ό 6

Question

What is rate of a chemical reaction? Explain average and instantaneous rate of reaction with help of graph and also give unit of rate of reaction.

Answer

Rate of a chemical reaction: The change in concentration of reactant or product in unit time is called rate of a chemical reaction.
It can be expressed in terms of:

(i) The rate in decrease in concentration of any one of the reactants.

(ii) The rate in increase in concentration of any one of the products.

Consider a hypothetical reaction, assuming that the volume of the system remains constant.
R β†’ P
One mole of the reactant R produces one mole of the product P.
If [R]1 and [P]1 are the concentrations of R and P respectively at time t1 and [R]2 and [P]2 are their concentrations at time t2 then,
βˆ†t = t2 – t1
βˆ†[R] = [R]2 – [R]1
βˆ†[P] = [P]2 – [P]1
(Square bracket expressing molar concentration.)
Rate of disappearance of
R = =
Rate of appearance of
P = = +
Above given equations represent the average rate of a reaction (rav).
Average rate depends upon the change in concentration of reactants or products and the time taken for that change to occur.
Instantaneous rate of reaction: Average rate cannot be used to predict the rate of a reaction at a particular instant because the rate is generally not constant throughout the reaction.
So, to express the rate at a particular moment of time we determine instantaneous rate.
Instantaneous rate is obtained when we consider the average rate at the smallest time interval say dt (when βˆ†t approaches zero).
Hence, mathematically for an infinitesimally small dt instantaneous rate is given by:
rav = –
As βˆ†t β†’ 0 or rinst = –
Unit of rate of a reaction: Units of rate are concentration time–1.
If concentration is in mol L–1 and time is in seconds then the units will be mol L–1sec–1.
However, in gaseous reactions, when the concentration of gases is expressed in terms of their partial pressure, then the units of the rate equation will be atm s–1.
#2 SUB πŸ–Ό 1

Question

Explain the rate expression for a reaction in which stoichiometric coefficients of reactants and products are not same or unit.

Answer

For reaction, n1A + n2B β†’ n3C + n4D
Rate of reaction:
For expressing the rate of such a reaction where stoichiometric coefficients of reactants or product are not equal to one, rate of disappearance of any of the reactants or the rate of appearance of the products is divided by their respective stoichiometric coefficients.
For reaction, Hg(l) + Cl2(g) β†’ HgCl2(s)
where stoichiometric coefficients of the reactants and products are same, then rate of the reaction is given as:
Rate of reaction =
For reaction, 2Hl(g) β†’ H2(g) + I2(g) the rate of decomposition of HI is twice the rate of formation of H2 or I2, to make them equal, the term βˆ†[HI] is divided by 2. The rate of this reaction is given by:
Rate of reaction =
Similarly for the reaction:
5Br–(aq) + BrO3–(aq) + 6H+(aq) β†’ 3Br2(aq) + 3H2O(l)
Rate =
=
#3 SUB 3M πŸ–Ό 3

Question

Explain rate law and rate constant with an example.

Answer

Rate of a reaction depends upon the concentration of reactants.
Consider a general reaction
aA + bB β†’ cC + dD
where a, b, c and d are the stoichiometric coefficients of reactants and products.
The rate expression for this reaction is
Rate Ξ±[A]x[B]y
where exponents x and y may or may not be equal to the stoichiometric coefficients (a and b) of the reactants.
Above equation can also be written as
Rate = k[A]x[B]y
= k[A]x[B]y
This form of equation is known as differential rate equation, where k is proportionality constant called rate constant.
The equation which relates the rate of reaction to concentration of reactants is called rate law or rate expression.
Thus, rate law is the expression in which reaction rate is given in terms of molar concentration of reactants with each term raised to some power, which may or may not be same as stoichiometric coefficient of the reacting species in a balanced equation.
For example: 2NO(g) + O2(g) β†’ 2NO2(g)
The rate equation for this reaction will be:
Rate = k[NO]2[O2]
This differential form of this rate expression is given as:
= k[NO]2[O2]
Some other examples are given below:

1. CHCl3 + Cl2 β†’ CCl4 + HCl

2. CH3COOC2H5 + H2O β†’ CH3COOH + C2H5OH

Experimental rate expression:
Rate = k[CHCl3] Β·
Rate = k[CH3COOC2H5][H2O]0
In these reactions, the exponents of the concentration terms are not the same as their stoichiometric coefficients. Thus, we can say that:
Rate law for any reaction cannot be predicted by merely looking at the balanced chemical equation. i.e. theoretically but must be determined experimentally.
#4 SUB 3M πŸ–Ό 4

Question

What is order of reaction ? Discuss elementary and complex reactions, Explain units of rate constant in detail.

Answer

The sum of power of the concentration of the reactants in the rate law expression is called the order of that chemical reaction.
For reaction: aA + bB β†’ product
Rate = k[A]x[B]y x and y indicate how sensitive the rate is to change in concentration of A and B.
Sum of these exponents, i.e. x + y gives the overall order of a reaction whereas x and y represent the order with respect to the reactants A and B respectively.
Order of reaction can be 0, 1, 2, 3 and even a fraction.
A zero order reaction means that the rate of reaction is independent of the concentration of reactants.
The reactions taking place in one step are called elementary reactions.
When a sequence of elementary reactions (called mechanism) gives us the products, that reactions are called complex reactions.
Units of rate constant:
For a general reaction
aA + bB β†’ cC + dD
Rate = k[A]x[B]y
where x + y = n = order of the reaction
k = =
(where [A] = [B])
Taking SI unit of concentration, mol L–1 and time, s, the unit of k for different reaction order listed in table.

Reaction

Order

Units of rate constant

Zero order reaction

0

= mol L–1 s–1

First order reaction

1

= s–1

Second order reaction

2

= mol–1 L s–1

#5 SUB 3M

Question

Write a note on molecularity of a reaction and its different types.

Answer

Molecularity of a reaction: The number of reacting species (atoms, ions or molecules) taking part in an elementary reaction, which must collide simultaneously in order to bring about a chemical reaction is called molecularity of a reaction.
For elementary reaction, order of a reaction and molecularity of a reaction are same.
The reaction can be unimolecular when one reacting species is involved. For example, decomposition of ammonium nitrite.
NH4NO2 β†’ N2 + 2H2O
Bimolecular reactions involve simultaneous collision between two species, for example, dissociation of hydrogen iodide. 2HI β†’ H2 + I2
Trimolecular or tetramolecular reactions involve simultaneous collision between three reacting species. For example, 2NO + O2 β†’ 2NO2
The probability that more than three molecules can collide and react simultaneously is very small. Hence, the reaction with the molecularity three are very rare and slow to proceed.
#6 SUB πŸ–Ό 3

Question

Explain how the molecularity of a complex reaction determined? Give the points showing difference between molecularity of a reaction and order of a reaction.

Answer

Term molecularity is only applicable to elementary reactions, even though to determine molecularity of a complex reaction it is necessary to know the mechanism of that reaction.
Through mechanism of a reaction we can have information about slowest step of reaction.
The overall rate of the reaction is controlled by the slowest step in a reaction called the rate determining step.
Consider the decomposition of hydrogen peroxide which is catalysed by iodide ion in an alkaline medium,
The rate equation for this reaction is found to be: Rate = –
This reaction is first order with respect to both and .
Mechanism involve two steps:
(1)
(2)
The first step, being slow, is the rate determining step.
Thus, the rate of formation of intermediate will determine the rate of this reaction.
Thus, it can be said that, for complex reaction, order is given by the slowest step and molecularity of the slowest step is same as the order of the overall reaction.
Difference between molecularity and order of a reaction:
(i) Order of a reaction is an experimental quantity. It can be zero and even a fraction but molecularity cannot be zero or a non integer.
(ii) Order is applicable to elementary as well as complex reactions whereas molecularity is applicable only for elementary reactions. For complex reaction molecularity has no meaning.
(iii) For complex reaction, order is given by the slowest step and generally molecularity of the slowest step is same as the order of the overall reaction.
#7 SUB 3M πŸ–Ό 4

Question

Derive integrated rate equation for zero order reaction and also explain how the rate constant can be determine with help of graph.

Answer

Zero order reaction means that the rate of the reaction is proportional to zero power of the concentration of reactants.
Consider the reaction.
R β†’ P
Rate of reaction for this reaction can be expressed as
Rate = = k[R]0
As any quantity raised to power zero is units.
Rate = = k Γ— 1
Thus, the rate of zero order reaction is independent from concentration of reactants.
d[R] = –k dt
Integrating both sides
[R] = –kt + I ... ... Eq. (1)
Where, I is the constant of integration
At t = 0, the concentration of the reactant
R = [R]0, where [R]0 is initial concentration of the reactant.
Substituting in equation (1)
[R]0 = –kx 0 + I
[R]0 = I
Substituting the value of I in the equation (1)
[R] = –kt + [R]0 ... ... Eq. (2)
Further simplifying equation (2)
k = ... ... Eq. (3)
Comparing equation (2) with equation of straight line, y = mx + c, if we plot [R] against t, we get a straight line with slope = –k and intercept equal to [R]0
#8 SUB 2M πŸ–Ό 1

Question

Give examples of zero order reaction.

Answer

Zero order reaction are relatively uncommon but they occur under special condition.
Some enzyme catalysed reaction and reaction which occur on metal surface are a few examples of zero order reactions.
The decomposition of gaseous ammonia on hot platinum surface is a zero order reaction at high pressure.
2NH3(g) N2(g) + 3H2(g)
Rate = k[NH3]0 = k
In this reaction, platinum metal acts as a catalyst.
At high pressure, the metal surface gets saturated with gas molecules.
So, a further change in reaction condition is unable to alter the amount of ammonia on the surface of the catalyst making rate of the reaction independent of its concentration.
The thermal decomposition of HI on gold surface is another example of zero order reaction.
#9 SUB 4M πŸ–Ό 18

Question

Derive integrated rate equation for first order reaction and also explain how the rate constant can be determine with help of graph.
OR
Derive the formula for Rate constant (k) and half life period for first order reaction.

Answer

First order reaction means that the rate of reaction is proportional to the first power of the concentration of the reactant R.
For example, consider the following reaction
R β†’ P
Rate of reaction for this reaction can be expressed as
Rate = = k[R]
Or = –kdt
Integrating this equation, we get
ln [R] = –kt + I ... ... Eq. (1)
where, I is the constant of integration and its value can be determined easily.
When t = 0, R = [R]0, where [R]0 is the initial concentration of the reactant.
Therefore, equation (1) can be written as
ln [R]0 = –k Γ— 0 + I
ln [R]0 = I
Substituting the value of I in equation (1)
ln [R] = –kt + ln [R]0 ... ... Eq. (2)
Rearranging this equation
ln = –kt
or k = ln ... ... Eq. (3)
At time t1 from equation (1)
ln [R]1 = – kt1 + ln [R]0 ... ... Eq. (4)
At time t2
ln [R]2 = – kt2 + ln [R]0 ... ... Eq. (5)
where, [R]1 and [R]2 are the concentration of the reactants at time t1 and t2 respectively.
Subtracting Eq. (5) from (4)
ln [R]1 – ln [R]2 = –kt1 – (–kt2)
ln = k(t2 – t1)
k = ln ... ... Eq. (6)
So, equation (2) can also be written as
ln = –kt
Taking antilog of both the sides
[R] = [R]0 e–kt ... ... Eq. (7)
Comparing equation (2) with y = mx + c, if we plot ln [R] against t, we get a straight line with slope = – k and intercept equal to ln [R]0
The first order rate equation (3) can also be written in the form
k = log ... ... Eq. (8)
or log
If we plot a graph between log vs t,
the slope =
#10 SUB 2M πŸ–Ό 3

Question

Give examples of first order reaction.

Answer

Hydrogenation of ethene is an example of first order reaction.
C2H4(g) + H2(g) β†’ C2H6(g)
Rate = k[C2H4]
All natural and artificial radioactive decay of unstable nuclei take place by first order kinetics.
β†’ +
Rate = k[Ra]
Decomposition of N2O5 and N2O are some more examples of first order reactions.
#11 SUB πŸ–Ό 2

Question

Derive integrated rate equation for first order reaction containing gaseous components.

Answer

Let us consider a typical first order gas phase reaction.
A(g) β†’ B(g) + C(g)
Let pi be the initial pressure of A and pt the total pressure at time β€˜t’. Integrated rate equation for such a reaction can be derived as
Total pressure pt = pA + pB + pC (pressure units)
pA, pB and pC are partial pressures of A, B and C respectively. If x atm can be the decrease in pressure of A at time t and one mole each of B and C is being formed. The increase in pressure of B and C will also be X atm each
A(g) β†’ B(g) + C(g)
At t = 0 pi atm 0 atm 0 atm
At time t (pi– x) atm x atm x atm
where, pi is the initial pressure at time t = 0.
pt = (pi – x) + x + x = pi + x
x = (pt – pi)
where, pA = pi – x = pi – (pt – pi) = 2pi – pt
k =
= log
#12 SUB 3M πŸ–Ό 23

Question

What is half-life of a reaction? Derive formula for half-life of zero and first order reaction.
OR
Derive equation of rate constant and half life of reaction for the zeroth order reaction.

Answer

Half-life of a reaction: The time in which the concentration of a reactant is reduced to one half of its initial concentration is called half-life of a reaction.
Half-life for zero order reaction:
For a zero order reaction, rate constant is given by following equation
k =
At t = , [R] = [R]0
The rate constant at becomes
k =
=
It is clear that for a zero order reaction is directly proportional to the initial concentration of the reactants and inversely proportional to the rate constant.
Half-life for first order reaction:
For the first order reaction,
k = log
at t = [R] =
So, the above equation becomes
k = log
or = log2
= Γ— 0.301
=
It can be seen that for a first order reaction, half-life period is constant, i.e. it is independent of initial concentration of the reacting species.
The half-life of a first order equation is readily calculated from the rate constant and vice versa.
For zero order reaction Γ— [R]0 for first order reaction is independent of [R]0
#13 SUB πŸ–Ό 2

Question

Explain pseudo first order reaction with example.

Answer

The order of a reaction is sometimes altered by conditions.
There are many reactions which obey first order rate law although they are higher order reactions.
Consider the hydrolysis of ethyl acetate which is a chemical reaction between ethyl acetate and water. In reality, it is second order reaction and concentration of both ethyl acetate and water affect the rate of the reaction.
But water is taken in large excess for hydrolysis, therefore, concentration of water is not altered much during the reaction.
Thus, the rate of reaction is affected by concentration of ethyl acetate.
For e.g. 0.01 mol ethyl acetate react with 10 mol of water amounts of the reactants and products at the beginning (t = 0) and completion (t) of the reaction are give as under.
CH3COOC2H5 + H2O CH3COOH + C2H5OH
t = 0 0.01 mol 10 mol 0 mol 0 mol
t = t 0 mol 9.99 mol 0.01 mol 0.01 mol
The concentration of water does not get altered much during the course of the reaction. So, the reaction behaves as first order reaction. Such reactions are called pseudo first order reactions.
Inversion of cane sugar is another pseudo first order reaction.
C12H22O11 + H2O C6H12O6 + C6H12O6
Cane sugar Glucose Fructose
Rate = k [C12H22O11]
#14 SUB 3M πŸ–Ό 2

Question

What is activation energy? Explain with the help of graph by suitable example.

Answer

Activation energy can be understood clearly using the formation reaction of hydrogen iodide.
H2(g) + I2(g) β†’ 2HI(g)
According to Arrhenius, this reaction can take place only when a molecule hydrogen and molecule of iodine collide to form an unstable intermediate. It exists for a very short time and then breaks up to form two molecules of hydrogen iodide.
Intermediate
The energy required to form this intermediate, called activated complex (C), is known as activation energy (Ea).
Below figure is obtained by plotting potential energy vs reaction coordinate. Reaction coordinate represents the profile of energy change when reactant change into products.
Some energy is released when the complex decomposes to form products. So, the final enthalpy of the reaction depends upon the nature of reactants and products.
#15 SUB 4M πŸ–Ό 10

Question

Derive the formula for determining activation energy from Arrhenius equation using rate constant at different temperatures and also explain how activation energy can be determined using graph.

Answer

Activation energy using graph:
Taking natural logarithm on both the side of Arrhenius equation k = Ae
ln k = + ln A ... ... Eq. (1)
The plot of ln k vs 1/T gives a straight line as shown in figure.
In figure, slope = and intercept = lnA. So, we can calculate activation energy (Ea) and Arrhenius constant A using these values.
Formula of activation energy: It has been found from Arrhenius equation that increasing the temperature or decreasing the activation energy will result in an increase in the rate of the reaction and an exponential increase in rate constant.
Thus, at temperature T1, equation (1) is
ln k1 = + lnA ... ... Eq. (2)
at temperature T2, equation (1) is
ln k2 = + lnA ... ... Eq. (3)
(since A is constant for given reaction)
k1 and k2 are rate constant at temperatures T1 and T2 respectively.
Subtracting equation (2) from (3), we obtain
lnk2 – lnk1 =
ln
log
log
From above formula activation energy can be calculate using measured values of rate constants at different temperatures.
#16 SUB 2M πŸ–Ό 2

Question

Explain the effect of catalyst on rate of reaction and also give its characteristics.
Or

Answer

Answer the following questions on catalyst:
(i) How it increases the rate of reaction.
(ii) Write any 4 characteristics of catalyst.
Ans. A catalyst is a substance which increase the rate of a reaction without itself undergoing any permanent chemical change.
For example, MnO2 catalyses the following reaction so as to increase its rate considerably.
2KClO3 2KCl + 3O2
The word catalyst should not be used when the added substance reduces the rate of reaction. The substance is then called inhibitor.
The action of catalyst can be explained by intermediate complex theory.
According to this theory, a catalyst participates in a chemical reaction by forming temporary bond with the reactants resulting in an intermediate complex.
It is believed that the catalyst provides an alternate path or reaction mechanism by reducing the activation energy between reactants and products hence lowering the potential energy barrier as shown in figure.
It is clear from Arrhenius equation that lower the value of activation energy faster will be the rate of reaction.
This has transitory existence and decomposes to yield products and the catalyst.
Characteristics of catalyst:
A small amount of catalyst can catalyses a large amount of reactants.
A catalyst does not alter Gibbs energy of a reaction.
It catalysis the spontaneous reaction but does not catalyze the non-spontaneous reactions.
It is also found that a catalyst does not change the equilibrium constant of a reaction rather, it helps in attaining the equilibrium faster, that is, it catalyses the forward as well as backward reaction to the same extent so that the equilibrium state remains same but is reached earlier.
#17 SUB 2M πŸ–Ό 1

Question

Write Arrhenius equation. Explain the terms involved in it.

Answer

The temperature dependence of the rate of a chemical reaction can be accurately explained by Arrhenius equation.
k = A
Where, A is the Arrhenius factor or frequency factor. It is also called per-exponential factor. It is a constant specific to a particular reaction. R is gas constant and Ea is activation energy measured in joules/mole (J mol–1).
#18 SUB 4M πŸ–Ό 4

Question

Write a note on collision theory of chemical reaction.
Or
What is meant by collision theory? Explain.

Answer

Collision theory, which was developed by Max Trautz and William Lewis in 1916-18, provides greater insight into the energetic and mechanistic aspects of reaction.
It is based on kinetic theory of gases.
According to this theory, the reactant molecules are assumed to be hard spheres and reaction is postulated to occur when molecules collide with each other.
The number of collision per second per unit volume of the reaction mixture is known as collision frequencyΒ (Z).
Another factor which affects the rate of chemical reaction is activation energy.
For a bimolecular elementary reaction;
A + B β†’ Products
Rate of reaction can be expressed as:
Rate = ZAB ... ... Eq. (1)
where ZAB represents the collision frequency of reactants A and B, and represents the fraction of molecules with energies equal to or greater than Ea.
Comparing equation (1) with Arrhenius equation, we can say that A is related to collision frequency.
Equation (1) predicts the value of rate constant fairly accurately for the reaction that involve atomic species or simple molecule but for complex molecules significant deviations are observed.
The reason could be that all collision do not lead to the formation of products.
The collision in which molecules collide with sufficient kinetic energy (called threshold energy) and proper orientation, so as to facilitate breaking of bonds between reacting species and formation of new bonds to form products are called as effective collision.
For example, formation of methanol from bromomethane CH3Br + OH – β†’ CH3OH + Br– depends upon the orientation of reactant molecule as shown in figure.
The proper orientation of reactant molecules lead to bond formation whereas improper orientation makes them simply bounce back and no product are formed.
To account for effective collision, another factor P, called the probability factor or steric factor is introduced.
It takes into account the fact that in a collision, molecules be properly oriented i.e.
Rate = PZAB
Thus, in collision theory activation energy and proper orientation of the molecules together determine the criteria for an effective collision and hence the rate of chemical reaction.
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#19 SUB 2M πŸ–Ό 4

Question

For the reaction R β†’ P, the concentration of a reactant changes from 0.03 M to 0.02 M in 25 minutes. Calculate the average rate of reaction using units of time both in minutes and seconds.

Answer

Average rate =
=
=
=
= 4 Γ— 10–4 M min–1
Rate of reaction in terms of second
=
= 6.67 Γ—10–6 M s–1
#20 SUB 2M πŸ–Ό 3

Question

In a reaction, 2A β†’ Products, the concentration of A decreases from 0.5 mol L–1 to
0.4 mol L–1 in 10 minutes. Calculate the rate during this interval ?

Answer

For reaction 2A β†’ Product,
βˆ†t = 10 min
Rate =
=
= mol L–1 min–1
= 5.0 Γ—10–3 M min–1
#21 SUB 1M πŸ–Ό 2

Question

For reaction A + B β†’ Product; the rate law is given by, r = k[A][B]2 What is the order of the reaction?

Answer

Overall order of reaction is equal to the sum of powers of the concentration of reactants
Here, order of the reaction = + 2 = 2.5
#22 SUB 2M πŸ–Ό 1

Question

The conversion of molecules X to Y follows second order kinetics. If concentration of X is increased to three times How will it affect that rate of formation of Y?

Answer

X β†’ Y is a second order reaction,
Therefore, rate law can be expressed as
V1 = k[X]2
If the concentration of X is increased three time, then the new concentration will be 3X and the new rate will be
V2 = k[3X]2 = 9k[X]2
Taking ratio of V2 and V1, we get
V2 = 9V1
Hence the rate of formation of Y will increase by 9 times.
#23 SUB 3M πŸ–Ό 5

Question

A first order reaction has a rate constant
1.15 Γ— 10–3 s–1. How long will 5 g of this reactant take to reduce to 3 g ?

Answer

Integrated rate equation for first order reaction,
k = log
[R]0 = 5 g and [R] = 3 g, k = 1.15 Γ— 10–3 s–1
Substituting above values in equation
t = log
t = log
#24 SUB 2M πŸ–Ό 4

Question

Time required to decompose SO2Cl2 to half of its initial amount is 60 minutes. If the decomposition is a first order reaction, then calculate the rate constant of the reaction.

Answer

Time required to decompose half of the reagent is 60 minutes, i.e. = 60 min.
For first order reaction, relation between half-life and rate constant k is
k = = 0.01155 min–1 OR
k = = 1.925 Γ—10– 4 s–1
#25 SUB 2M

Question

Explain effect of temperature on rate constant.
Or
What will be the effect of temperature on rate constant?

Answer

Most of the chemical reactions are accelerated by increase in temperature.
For example, in decomposition of N2O5, the time taken for half of the original amount of material to decompose is 12 min at 50Β°C, 5 h at 25Β°C and 10 days at 0Β°C.
In a mixture of potassium permanganate and oxalic acid, potassium permanganate gets decolourised faster at a higher temperature than that at a lower temperature.
It has been found that for a chemical reaction with rise in temperature by 10Β°, the rate constant is nearly doubled.
#26 SUB 3M πŸ–Ό 3

Question

The rate of the chemical reaction doubles for an increase of 10K in absolute temperature from 298K, calculate Ea.

Answer

log =
Here, T1 = 298K, T2 = 298 + 10K = 308K
R = 8.314 J K–1 mol–1
The rate of chemical reaction doubles for an increase of 10K in absolute temperature, therefore = 2.
Substituting the values in above equation, we get
log 2.0 =
Ea =
Ea =
Ea = 52897.77 J mol–1 = 52.89777 kJ mol–1
#27 SUB 3M πŸ–Ό 4

Question

The activation energy for the reaction 2HI(g) β†’ H2 + I2(g) is 209.5 kJ mol–1 at
581K. Calculate the fraction of molecules of reactants having energy equal to or greater than activation energy.

Answer

The fraction of molecules of reactants having energy equal to or greater than activation energy x =
Taking 10 base log on both the sides,
log x =
∴ log x =
∴ log x = –18.8323
∴ x = antilog (–18.8323) = .1677
∴ The fraction of molecules of reactants having energy equal to or greater than activation energy
x = 1.471 Γ— 10–19
S src: NCERT Textbook Exercise Questions And Answers match 75% type: 30 Q – Export ZIP
#28 SUB 2M πŸ–Ό 10

Question

From the rate expression for the following reactions, determine their order of reaction and the dimensions of the rate constants.
(i) 3NO(g) β†’ N2O(g) + NO2(g); Rate = k[NO]2
(ii) H2O2(aq) + 3l–(aq) + 2H+ β†’ 2H2O(l) + I3–;
Rate = k[H2O2][I –]
(iii) CH3CHO(g) β†’ CH4(g) + CO(g);
Rate = k[CH3CHO]
(iv) C2H5Cl(g) β†’ C2H4(g) + HCl(g);
Rate = k[C2H5Cl]

Answer

(i) 3NO(g) β†’ N2O(g) + NO2(g)
Rate = k[NO]2
∴ Order of reaction = 2
Dimension of the rate constant:
Rate = k[NO]2
k = = = mol–1 L s–1
(ii) H2O2(aq) + 3I –(aq) + 2H+ β†’ 2H2O(l) + I3–
Rate = k[H2O2][I –]
Order of reaction with respect to H2O2 = 1
order of reaction with respect to l–1 = 1
∴ overall order of reaction = 2
Dimension of the rate constant.
Rate = k[H2O2][I–]
k =
=
= mol–1 L s–1
(iii) CH3CHO(g) β†’ CH4(g) + CO(g)
Rate = k[CH3CHO]
∴ Order of reaction =
Dimension of the rate constant
Rate = k[CH3CHO]
k =
=
=
(iv) C2H5Cl(g) β†’ C2H4(g) + HCl(g)
Rate = k[C2H5Cl]
∴ Order of reaction = 1
Dimension of the rate constant.
Rate = k[C2H5Cl]
k =
= = s–1
#29 SUB 3M πŸ–Ό 1

Question

For the reaction: 2A + B β†’ A2B
the rate = k[A][B]2 with k = 2.0 Γ— 10–6 mol–2 L2 s–1. Calculate the initial rate of the reaction when [A] = 0.1 mol L–1,
[B] = 0.2 mol L–1, Calculate the rate of reaction after [A] is reduce to 0.06 mol L–1

Answer

Initial rate = k[A][B]2
= 2.0 Γ— 10–6 mol–2 L2 s–1 Γ— 0.1 mol L–1
Γ— (0.2 mol L–1)2
= 8.0 Γ— 10–9 mol L–1 s–1
Concentration of A is reduce to 0.06 mol L–1
Concentration of [A] reacted = 0.10 – 0.06
= 0.04 mol L–1
As per the reaction, 2A + B β†’ A2B
Half of the concentration of B is reduce then A
∴ Concentration of [B] reacted = X 0.04
= 0.02 mol L–1
[B] = 0.2 – 0.02 = 0.18 mol L–1
Rate = k [A][B]2
= 2.0 Γ— 10–6 mol–2 L2 s–1 Γ— 0.06 mol L–1
Γ— (0.18 mol L–1)2
= 3.88 Γ— 10–9 mol L–1 s–1
#30 SUB 2M πŸ–Ό 6

Question

The decomposition of NH3 on platinum surface is zero order reaction. What are the rates of production of N2 and H2 if k = 2.5 Γ— 10– 4
mol L–1 s–1 ?

Answer

The decomposition reaction of ammonia is
2NH3(g) β†’ N2(g) + 3H2(g),
This is zero order reaction,
Rate = =
= = k[NH3]0
Rate of appearance of N2 =
= k[NH3]0 = k
= 2.5 Γ— 10–4 mol L–1 s–1
Rate of appearance of H2 =
= k[NH3]0 = k
∴ = 3k = 3 Γ— 2.5 Γ— 10– 4 mol L–1 s–1
= 7.5 Γ— 10–4 mol L–1 s–1
#31 SUB πŸ–Ό 5

Question

The decomposition of dimethyl ether leads to the formation of CH4, H2 and CO and the reaction rate is given by Rate = k[CH3OCH3]
The rate of reaction is followed by increase in pressure in a closed vessel. So the rate can also be expressed in terms of the partial pressure of dimethyl ether i.e. Rate =
If the pressure is measured in bar and time in minutes, then what are the units of rate and rate costants ?

Answer

The pressure is measured in bar and time in minutes,
So, the unit of rate = Bar min–1
Unit of K =
=
= min–1
#32 SUB

Question

Mention the factors that affect the rate of a chemical reaction.

Answer

Factors affecting the rate of a chemical reaction:
(i) Nature of reactant: If intermolecular attraction force between reactant molecules is more or bond enthalpy of reactant molecule is more than more energy of activation is required, so that the rate of reaction becomes slow.
(ii) Concentration of reactant: More is the concentration of reactant, more will be the rate of reaction.
(iii) Pressure: On increasing pressure, the collision between reactant molecule increases, which results in to increase in the rate of reaction.
(iv) Temperature: In most of the cases, on increasing temperature the rate of reaction and rate constant both increase.
For endothermic reaction the rate of reaction increases on increasing temperature, whereas for exothermic reaction the rate of reaction decreases on increasing temperature.
(v) Catalyst: The energy of activation decreases on using catalyst. Thus the value of energy barrier decreases for reaction, hence the rate of reaction increases.
#33 SUB 2M πŸ–Ό 4

Question

A reaction is second order with respect to a reactant. How is the rate of reaction affected if the concentration of the reactant is
(i) doubled (ii) reduced to half ?

Answer

Reaction β†’ Products
Rate r1 = k[A]2
(i) When concentration of reactant is doubled;
Rate r2 = k[2A]2 = 4k[A]2 = 4r1
∴ When concentration of the reactant is doubled, the rate of reaction will become 4 times of the initial rate.
(ii) When concentration of reactant is reduced to half;
Rate r2 = = k[A]2 =
∴ when concentration of the reactant is reduced by half, the rate of reaction will be reduce to of the initial rate.
#34 SUB 2M πŸ–Ό 2

Question

What is the effect of temperature on the rate constant of a reaction? How can this effect of temperature on rate constant be represented quantitatively?

Answer

Most of the chemical reactions are accelerated by increase in temperature.
Increasing the temperature will result in an exponential increase in the rate constant.
It has been found that for a chemical reaction with rise in temperature by 10Β°, the rate constant is nearly doubled.
Rate = (2)
According to Swedish chemist Arrhenius, the quantitative effect of temperature on the rate constant can be express by following equation.
k = A
Where, A = Arrhenius factor or frequency factor.
R = gas constant
Ea = activation energy in terms of
joules/mole (J mol–1).
#35 SUB 2M πŸ–Ό 4 β–¦ 1

Question

In a pseudo first order reaction in water, the following results were obtained:
calculate the average rate of reaction between the time interval 30 to 60 second.

Time/s

0

30

60

90

[A]/mol L–1

0.55

0.31

0.17

0.085

Answer

Hydrolysis of ester is pseudo first order reaction.
RCOOR' + H2O RCOOH + R'OH
Ester Water Acid Alcohol
Average rate of reaction rav =
rav = –
[R]2 = concentration at 60 s = 0.17 M
[R]1 = concentration at 30 s = 0.31 M
rav =
rav = = 4.67 Γ— 10–3 mol L–1 s–1
#36 SUB 2M

Question

A reaction is first order in A and second
order in B.
(i) Write the differential rate equation. [June 2025]
(ii) How is the rate affected on increasing the concentration of B three times ?
(iii) How is the rate affected when the concentration of both A and B are doubled ?
[Topic 3.2] [June 2025] [2 Marks]

Answer

The given reaction is first order in A and second order in B.
(i) Rate = k[A][B]2
(ii) Initial rate r1 = k[A][B]2
When concentration of B is increased to three times,
Rate r2 = k[A][3B]2 = 9k [A][B]2 = 9r1

∴ Rate becomes nine times.

(iii) Initial rate r1 = k[A][B]2
When concentration of both A and B is increased to two times,
Rate r2 = k[2A][2B]2 = 8k [A][B]2 = 8r1
∴ Rate becomes eight times.
#37 SUB 4M πŸ–Ό 3 β–¦ 1

Question

In a reaction between A and B, the initial rate of reaction (r0) was measured for different initial concentrations of A and B as given below:

A/mol L–1

0.20

0.20

0.40

B/mol L–1

0.30

0.10

0.05

r0/mol L–1 s–1

5.07 Γ— 10–5

5.07 Γ— 10–5

1.43 Γ— 10–4

Answer

Suppose,
Order of reaction with respect to A = x
Order of reaction with respect to B = y
Then,
Rate = k[A]x[B]y
∴ r1 = k[0.20]x[0.30]y = 5.07 Γ—10–5 ... ... (1)
r2= k[0.20]x[0.10]y = 5.07 Γ—10–5 ... ... (2)
r3 = k[0.40]x [0.05]y = 1.43 Γ—10– 4 ... ... (3)
Dividing (1) and (2) we get,
∴ = [3]y = 1
∴ y = 0, because [3]0 = 1 = [3]y
Dividing (3) and (2) we get,
= 2.82
∴ = 2.82
∴ [2]x = 2.82
Taking log of both the side we get,
log[2]x = log2.82
∴ x log2 = log2.82
x Γ— 0.3010 = 0.4503
∴ x = = 1.5
∴ order of reaction with respect to A = 1.5
order of reaction with respect to B = 0
#38 SUB 4M πŸ–Ό 2 β–¦ 1

Question

The following results have been obtained during the kinetic studies of the reaction:
2A + B β†’ C + D
Determine the rate law and the rate constant for the reaction.

Experiment

[A]

[B]

Initial rate of formation of
D/mol L
–1 min–1

mol L–1

mol L–1

I

0.1

0.1

6.0 Γ— 10–3

II

0.3

0.2

7.2 Γ— 10–2

III

0.3

0.4

2.88 Γ— 10–1

IV

0.4

0.1

2.40 Γ— 10–2

Answer

Suppose,
Order of reaction with respect to A = x
Order of reaction with respect to B = y
∴ Rate = k[A]x[B]y
∴ r1 = k[0.1]x[0.1]y = 6.0 Γ— 10–3 ... ... (1)
r2 = k[0.3]x[0.2]y = 7.2 Γ— 10–2 ... ... (2)
r3 = k[0.3]x[0.4]y = 2.88 Γ— 10–1... ... (3)
r4 = k[0.4]x[0.1]y = 2.40 Γ— 10–2... ... (4)
Dividing (4) and (1) we get,
∴ = [4]x = [4]1
Order of reaction with respect to A = 1
Dividing (3) and (2) we get,
∴ = [2]y = 4 = [2]2
∴ y = 2
∴ order of reaction with respect to A = 1
order of reaction with respect to B = 2
overall order of reaction = 3
∴ rate equation,
Rate = k[A]1[B]2
Calculation of rate constant k
From equation (1)
r1 = k[0.1]1[0.1]2 = 6.0 Γ— 10–3
k =
=
= 6.0 mol–2 L–2 min–1
#39 SUB 3M πŸ–Ό 3 β–¦ 1

Question

The reaction between A and B first order with respect to A and zero order with respect to B. Fill the blanks in the following table:

Experiment

[A]

[B]

Initial rate/

mol L–1 min–1

mol L–1

mol L–1

I

0.1

0.1

2.0 Γ— 10–2

II

–

0.2

4.0 Γ— 10–2

III

0.4

0.4

–

IV

–

0.2

2.0 Γ— 10–2

Answer

Reaction A β†’ B
Rate = k[A]1[B]0
Tate constant in Experiment-I:
Rate = k[A]
∴ k =
∴ k = 2.0 Γ— 10–1 = 0.2 min–1
[A] in Experiment-II:
Rate = k[A]
∴ [A] =
∴ [A] = 0.2 mol L–1
Initial rate in Experiment-III:
Rate = k[A]
∴ rate = 0.2 Γ— 0.4 = 0.08 mol L–1 min–1
[A] in Experiment-IV:
Rate = k[A]
∴ [A] =
∴ [A] = 0.1 mol L–1
#40 SUB 1M πŸ–Ό 8

Question

Calculate the half-life of a first order reaction from their rate constants given below:
(1) 200 s–1 (ii) 2 min–1 (iii) 4 years–1

Answer

For first order reaction =
(i) = 3.465 Γ— 10–3 s
(ii) = 0.3465 min
(iii) = 0.17325 year
#41 SUB 4M πŸ–Ό 9

Question

The half-life for radioactive decay of 14C is 5730 years. An archaeological artifact containing wood had only 80% of the 14C found in a living tree. Estimate the age of the sample.

Answer

Half-life of 14C = 5730 years.
All radioactive decay follows first order kinetics.
k =
k = year–1
For first order reaction.
t = log
t = log
t = log1.25
t = Γ— 0.0969
t = 1845.2 years.
#42 SUB 4M πŸ–Ό 13 β–¦ 1

Question

The experimental data for decomposition of N2O5; [2N2O5 β†’ 4NO2 + O2]
in gas phase at 318K are given below:
(i) Plot [N2O5] against t.
(ii) Find the half-life period for the reaction.
(iii) Draw a graph between log [N2O5] and t
(iv) What is the rate law?
(v) Calculate the rate constant.
(vi) Calculate the half-life period from k and compare it with (ii).

Time/s

0

400

800

1200

1600

2000

2400

2800

3200

102Γ— [N2O5]

mol L–1

1.63

1.36

1.14

0.93

0.78

0.64

0.53

0.43

0.35

Answer

(i)
(ii) Initial concentration of N2O5
= 1.63 Γ— 10–2 M
Half of this concentration = 0.815 Γ— 10–2 M
From graph, time corresponding to this concentration is 1400 s.
Hence, = 1400 s.
(iii) First we will find values of log [N2O5],

Time/(sec)

[N2O5] Γ— 10+2

mol L–1

log[N2O5]

0

1.63

– 1.79

400

1.36

– 1.87

800

1.14

– 1.94

1200

0.93

– 2.03

1600

0.78

– 2.11

2000

0.64

– 2.19

2400

0.53

– 2.28

2800

0.43

– 2.37

3200

0.35

– 2.46

(iv) As plot of log [N2O5] β†’ t is straight line. Hence, it is first order reaction.
∴ Rate = k [N2O5]
(v) From plot of log [N2O5] β†’ t
Slope =
∴ k = – slope Γ— 2.303
= Γ— 2.303
= Γ— 2.303
= 4.82 Γ— 10–4 s–1
OR
From formula of integrated rate law for first order reaction,
k = log
∴ k = log
∴ k = log4.6571
∴ k = Γ— 0.6681
∴ k = 4.81 Γ— 10– 4 s–1
(vi) = =
= 0.1437 Γ— 104 s = 1437 s
Hence, half-life from both (ii) and (vi) are nearly same.
#43 SUB 3M πŸ–Ό 7

Question

The rate constant for a first order reaction is 60 s–1. How much time will it take to reduce the initial concentration of the reactant to its 1/16th value ?

Answer

Rate constant k = 60 s–1
If, initial concentration = [R]0 M
Then, concentration at time t = M
For first order reaction,
t = log
= log
= log16
= Γ— 1.2044
= 4.62 Γ— 10-2 Sec.
#44 SUB 3M πŸ–Ό 21

Question

During nuclear explosion, one of the products is 90Sr with half-life of 28.1 years. If 1 mg of 90Sr was absorbed in the bones of a newly born baby instead of calcium. How much of it will remain after 10 years and 60 years if it is not lost metabolically.

Answer

Nuclear explosion is first order reaction.
= 28.1 years and [R]0 = 1 Β΅g.
For first order reaction,
k = = = 2.466 Γ— 10–2 year–1
Calculation for amount of 90Sr remain after 10 years:
t = log
∴ log =
∴ log =
∴ log = 0.1070
∴ = anti log0.1070 = 1.2794
∴ [R]t = = 0.7816 ¡g 90Sr is left after 10 years.
Calculation for amount of 90Sr remain after
60 years:
t = log
∴ log =
∴ log =
∴ log = 0.6425
∴ = antilog 0.6425 = 4.39
∴ [R]t = = 0.228 ¡g 90Sr is left after 60 years.
#45 SUB 3M πŸ–Ό 13

Question

For a first order reaction, show that time required for 99% completion is twice the time required for the completion of 90% of reaction.

Answer

For first order reaction,
t99% = log ... ... (1)
t90% = log ... ... (2)
Taking ratio of equation (1) and (2)
=
∴ =
∴ =
∴ =
∴ = 2
∴ t99% = 2 Γ— t90%
#46 SUB 2M πŸ–Ό 14

Question

A first order reaction takes 40 min for 30% decomposition. Calculate the half-life period for the reaction .

Answer

uppose initial concentration [R]0 = 100
∴ Concentration at time t [R]t = 70, (30% decomposition).
t = 40 min.
Comparing k = log and
k = we get,
= log
∴ = log = Γ— 0.1549
∴ = 0.0089185
∴ = = 77.7 min
#47 SUB 4M πŸ–Ό 12 β–¦ 1

Question

For the decomposition of azoisopropane to hexane and nitrogen at 543K, the following data are obtained.
Calculate the rate constant.

Time (sec)

0

360

720

P(mm Hg)

35.0

54.0

63.0

Answer

Decomposition reaction of azoisopropane,
(CH3)2CHN = NCH(CH3)2 β†’ C6H14(g) + N2(g)

Pressure at

time t = 0

35 mm Hg

0

0

Change in

pressure

– x

+x

+x

Pressure after

t = 360 s

35 – x

+x

+x

∴ Total pressure after 360 s = 35 – x + x + x = 54 mm Hg
∴ Pressure after t = 360 s; 35 – 19 mm Hg = 16 mm Hg
Rate constant at 360 s:
Initial pressure [R]0 = pi = 35 mm Hg
Pressure at time t [R]t = pt = 16 mm Hg
For first order reaction,
k = log
= log
= log2.1875
= Γ— 0.3399
∴ k = 2.1747 Γ— 10–3 sec–1
k at t = 720 s:
Total pressure at t = 720 s,
Total pressure at equilibrium = 35 – x + x + x
= 63 mm Hg
Initial pressure at time t = 0 s, [R]0 = pi = 35 mm Hg
Pressure at time t = 720 s, [R]t = pt = 35 – 28
= 7 mm Hg
For first order reaction,
k = log
= log
= log5
= Γ— 0.6990
∴ k = 2.21 Γ— 10–3 sec–1
#48 SUB 4M πŸ–Ό 5 β–¦ 1

Question

The following data were obtained during the first order thermal decomposition of SO2Cl2 at a constant volume.
SO2Cl2(g) β†’ SO2(g) + Cl2(g)
Calculate the rate of reaction when total pressure is 0.65 atm.

Experiment

Time/s–1

Total pressure/atm

1

0

0.5

2

100

0.6

Answer

Decomposition reaction of SO2Cl2,
SO2Cl2(g) β†’ SO2(g) + Cl2(g)
Pressure at time t = 0 s pi atm 0 atm 0 atm
Pressure at time t pi – x atm x atm x atm
pi is initial pressure at time t = 0 s
∴ Total pressure at time t,
pt = pi – x + x + x = pi + x
∴ x = pt – pi
∴ p(SO2Cl2 ) = pi – x = pi – (pt – pi) = 2pi – pt atm.
For experiment - 1
At time t = 0 s, Initial pressure pi = 0.5atm
At time t = 100 s, p(SO2Cl2 ) = 2pi – pt
= 2 Γ— 0.5 – 0.6
= 0.4 atm
For first order reaction,
∴ k = log
= log
= Γ— 0.0969
∴ k = 2.2318 Γ— 10–3 sec–1
For experiment-2
At time t = 0 s, Initial pressure pi = 0.5 atm
pSO2Cl2 = 2pi – pt = 2 Γ— 0.5 – 0.65 = 0.35 atm
∴ rate = k βˆ™ pSO2Cl2
= 2.2318 Γ— 0.35 Γ— 10–3 sec–1
= 0.78113 Γ— 10–3
= 7.8113 Γ— 10–4 atm sec–1
#49 SUB 4M πŸ–Ό 11 β–¦ 2

Question

The rate constant for the decomposition of N2O5 at various temperatures is given below:
Draw a graph between lnk and 1/T and calculate the values of A and Ea. Predict the rate constant at 30Β° and 50Β°C.

T/Β°C

0

20

40

60

80

105 Γ— k/s–1

0.0787

1.70

25.7

178

2140

T/Β°C

T/K

k/s–1

lnk

1/T

0

273

0.0787 Γ— 105

= 78700

11.27

3.663 Γ— 10–3

20

293

1.70 Γ— 105

= 170000

12.04

3.412 Γ— 10–3

40

313

25.7 Γ— 105

= 2570000

14.76

3.195 Γ— 10–3

60

333

178 Γ— 105

= 17800000

16.69

3.003 Γ— 10–3

80

353

2140 Γ— 105

= 214000000

19.18

2.832 Γ— 10–3

Answer

Ea from the graph:
Slope =
∴ Ea = – slope Γ— R
∴ Ea = Γ— 8.314
∴ Ea = 94523.47 J mol-1 = 94.52347 kJ mol–1
Arrhenius constant from graph:
Intercept of graph shows value of ln A.
Intercept = 21.5
∴ ln A = 21.5
∴ 2.303 log A = 21.5
∴ log A = = 9.3356
∴ A = antilog 9.3356
∴ A = 2.1657 Γ— 109
The rate constant at 30Β°C and 50Β°C temperature:
T = 30Β°C = 303K
∴ = = 3.3 Γ— 10–3K–1
From graph, at = 3.3 Γ— 10–3K–1, ln k = 13.8
∴ 2.303 log k = 13.8
∴ log k = = 6
∴ k = antilog 6
∴ k = 1 Γ— 106 s–1
T = 50Β°C = 323K
∴ = = 3.09 Γ— 10–3K–1
From graph, at = 3.09 Γ— 10–3K–1, ln k = 16
∴ 2.303 log k = 16
∴ log k = = 6.9474
∴ k = antilog 6.9474
∴ k = 8.86 Γ— 106 s-1
#50 SUB 3M πŸ–Ό 3

Question

The rate constant for the decomposition of hydrocarbons is 2.418 Γ— 10–5 s–1 546K. If the energy of activation is 179.9 kJ/mol. What will be the value of pre-exponential factor.

Answer

Arrhenius equation,
logk = logA –
∴ logA = logk +
Here, T = 546K, k = 2.418Γ— 10–5 s–1
Ea = 179.9 kJ/mol = 179900 J/mol
A = ?
∴ logA = log2.418 Γ— 10–5 +
∴ logA = log2.418 + log 10–5 + 17.2082
∴ logA = 0.3834 – 5.0 + 17.2082
∴ logA = 12.5917
∴ A = antilog12.5917 = 3.9057 Γ— 1012 sec–1.
#51 SUB 3M πŸ–Ό 10

Question

Consider a certain reaction A β†’ Products with
k = 2.0 Γ— 10–2 s–1. Calculate the concentration of A remaining after 100 sec if the initial concentration of A is 1.0 mol L–1.

Answer

k = 2.0 Γ— 10–2 sec–1
[R]0 = 1 mol L–1, t = 100 sec
[R]t = ?
k = log
∴ log =
∴ log =
∴ log = 0.8684
∴ = anti log0.8684 = 7.3863
∴ [R]t = = = 0.1354 mol L–1
#52 SUB 3M πŸ–Ό 13

Question

Sucrose decompose in acid solution into glucose and fructose according to the first order rate law, with = 3.00 hours. What reaction of sample of sucrose remains after
8 hours?

Answer

For first order reaction,
k = = = 0.231 hour–1
Fraction of sample of sucrose remains after 8 hours:
Taking initial concentration [R]0 = 1 M,
Concentration after 8 hours [R]t = ?
k = log
∴ log =
∴ log =
∴ log = 0.8024
∴ = antilog 0.8024 = 6.3445
∴ [R]t = = = 0.1576 M
∴ The fraction of sample of sucrose that remains after 8 hours is 0.1576 M.
#53 SUB 3M πŸ–Ό 4

Question

The decomposition of hydrocarbon follows the equation k = (4.5 Γ— 1011 s–1) . Calculate
activation energy Ea.

Answer

Arrhenius equation,
k = A ... ... (I)
k = 4.5 Γ— 1011 s–1 ... ... (II)
Taking ratio of Eq. (I) and Eq. (II) we get,
Ea = 28000K Γ— R
Ea = 28000K Γ— 8.314 J K–1 mol–1
Ea = 232792 J mol-1 = 232.792 kJ mol–1
#54 SUB 4M πŸ–Ό 5

Question

The rate constant for the first order decomposition of H2O2 is given by the following equation:
log k = 14.34 – 1.25 Γ— 104 K/T
Calculate Ea for this reaction and at what temperature will its half-period be 256 minutes ?

Answer

Ea is the activation energy.
According to Arrhenius equation,
k = A
log k = logA – ... ... (I)
Now, log k = 14.34 – ... ... (II)
Comparing Eq. (I) and Eq. (II) we get,
Ea = 1.25 Γ— 104K Γ— 2.303 Γ— R
Ea = 1.25 Γ— 104K Γ— 2.303 Γ— 8.314 J K–1 mol–1
Ea = 23.93 Γ— 104 J mol–1 = 239.3 kJ mol–1
For first order reaction
k =
k = = 4.51 Γ— 10–5 s–1
For given equation,
log k = 14.34 –
log 4.51 Γ— 10-5 = 14.34 –
– 4.35 = 14.34 –
= 14.34 + 4.35 = 18.69
T = = 669K
#55 SUB 3M πŸ–Ό 4

Question

The decomposition of A into product has value of k as 4.5 Γ— 103 s–1 at 10Β°C and energy of activation 60 kJ mol–1. At what temperature would k be 1.5 Γ— 104 s–1 ?

Answer

A β†’ product
Here, T1 = 10Β°C = 283K
k1 = 4.5 Γ— 103 s–1
Ea = 60 kJ mol-1= 60000 J mol–1
k2 = 1.5 Γ— 104 s–1
T2 = ?
R = 8.314 J K–1 mol–1
log
log
0.5228 =
= 0.0001668
– 0.0001668
= 0.003534 – 0.0001668 = 0.003367
T2 = = 297.00 K
T2 = 297 – 273 = 24Β°C
#56 SUB 4M πŸ–Ό 12

Question

The time required for 10% completion of a first order reaction at 298K is equal to that required for its 25% completion at 308K. If the value of A is 4 Γ— 1010 s–1. Calculate k and activation energy (Ea)at 318K.

Answer

(A) Calculation of Ea:
(A) For first order reaction, k = log
At 298K temperature, k1 = log
... ... (I)
At 308K temperature, k2 = log
... ... (II)
Dividing Eq. (II) by Eq.(I) we get,
= 2.73
According to Arrhenius equation,
log
log2.73 =
Ea =
Ea = 76640 J/mol = 76.640 kJ/mol
(B) According to Arrhenius equation,
log k = logA –
log k = log4 Γ— 1010 –
log k = 10.6021 – 12.5870 = –1.9849 = .0151
k = antilog.0151
k = 1.035 Γ— 10–2 s–1
#57 SUB 3M πŸ–Ό 1

Question

The rate of a reaction quadruples when the temperature changes from 293K to 313K. Calculate the energy of activation of the reaction assuming that it does not change with temperature.

Answer

At T1 = 293K, rate constant = k1
At T2 = 313K, rate constant = k2 = 4k1
R = 8.314 J K–1 mol–1
According to Arrhenius equation,
log
log
Ea =
Ea =
Ea = 52863.33 J/mol = 52.863 kJ/mol
Class 12 Chemistry (Part 1) 013
S match 100% type: 1 Q – Export ZIP
#58 MCQ ⚠ needs answer review 1M πŸ–Ό 201 β–¦ 3

Question

(i)
(ii)
(iii)
1. During the decomposition of gas on the surface of a solid catalyst, at constant temperature the pressure of the gas at different time was observed to be as follows:
Then, what would be an order of reaction ?
2. If concentration of reactant changes from 0.03 M to 0.02 M in 25 seconds, then average rate of that reaction will be ______.
3. In the reaction 2A + 3B β†’ C + 4D, the rate of formation of product D is ______ times than that the rate of decrease in concentration of reactant B.
4. The units of rate of reaction are:
5. 2N2O5  4NO2 + O2
For the above reaction which of the following is not correct about rate of reaction?
6. On addition of AgNO3 to NaCl, white ppt. occurs:
7. Observe the following reaction,
2A + B β†’ C. The rate of formation of C is 2.2 Γ— 10–3 mol L–1 min–1. What is the value of – (mol L–1 min–1) ?
8. For reaction 2A + B β†’ 3C + D
Which of the following does not express the reaction of rate?
9. The differential rate expression for the reaction H2 + I2 β†’ 2HI is:
10. In the reaction
(aq) + 5Br–(aq) + 6H+ β†’ 3Br2(l) + 3H2O(l)
The rate of appearance of bromine (Br2) is related to rate of disappearance of bromide ions as following:
11. For a reaction, A+ 2B β†’ C, rate is given by + = k[A][B], hence, the order of the reaction is:
12. The rate of chemical reaction:
13. For a reaction A β†’ 2B, rate of disappearance of 'A' is related to the rate of appearance of B by the expression:
14. For a chemical reaction 2X + Y β†’ Z, the rate of appearance of Z is 0.05 mol L–1. The rate of disappearance of X will be:
15. For the reaction
N2 + 3H2  2NH3
The rate of change of concentration for hydrogen is 0.3 Γ— 10–4 M s–1. The rates of change of concentration of ammonia is:
16. The reaction; N2O5 in 2NO2 + O2(g) is of first order for N2O5 with rate constant
6.2 Γ— 10–4 s–1. What is the value of rate of reaction when [N2O5] = 1.25 mole L–1 ?
17. For the reaction N2 + 3H2 β†’ 2NH3, the rate
= 2 Γ— 10–4 M s–1. Therefore, the rate
– is given as:
18. The rate of a reaction is expressed in different ways as follows:
+ = = + =
The reaction is:
19. For the reaction, Cl2 + 2I– β†’ I2 + 2Cl–, the initial concentration of I– was 0.20 mol L–1 and the concentration after 20 min was 0.18 mol L–1. Then the rate of formation of I2 in mol L–1 would be:
20. For the reaction, N2O5 β†’ 2NO2 + O2
Given, – = k1[N2O5]
= k2[N2O5]
and = k3[N2O5].
The relation in between k1, k2 and k3 is:
21. The rate constant for the reaction,
2N2O5 β†’ 4NO2 + O2 is 3.0 Γ— 10–5 s–1. If the rate is 2.40 Γ— 10–5 then the concentration of N2O5 (in mol/L) is:
22. Among the following reactions, the fastest
one is:
23. For the reaction A + 2B β†’ C, the rate of reaction at a given instant can be given by:
24. The ionic reaction are usually very fast because:
25. In a reaction 2A β†’ Products; the concentration of A decreases from 0.5 mol litre–1 to
0.4 mol litre–1 in 10 minute. The rate of reaction during this interval is:
26. In the synthesis of ammonia by Haber process, if 60 moles of ammonia is obtained in one hour, then the rate of disappearance of nitrogen is:
27. The rate constant of a first order reaction is
3 Γ— 10–6 per second and initial concentration is 0.10 M. Then the initial rate of reaction is:
28. For the reaction N2(g) + 3H2(g) β†’ 2NH3(g) under certain condition of temperature and partial pressure of the reactants, the rate of formation of NH3 is 10–3 kg hr–1. The rate of conversion of H2 under same condition is:
29. With increase in temperature, rate of reaction:
30. In a gaseous phase reaction:
A2(g) β†’ B(g) + (1/2)C(g), the increase in pressure from 100 mm to 120 mm is noticed in 5 minutes. The rate of disappearance of A2 in mm
min–1 is:
31. The branch of chemistry which deals with the reaction rates and reaction mechanism is called:
32. For the reaction A β†’ B, if rate increase by 100 times on increasing concentration of reactant A from 0.1 M to 1 M. then what would be an order of reaction ?
33. The rate law for a reaction A(g) + B(g) β†’ Product (takes place in a close vessel) is
rate = k[A]2[B]. If the volume of vessel becomes half then what effect will be observed in the rate of reaction?
34. The value of rate constant for reaction
A + B β†’ Product is 4.5 Γ— 10-2 lit. mole-1 sec-1. If the concentration of A increase by two times the rate of reaction becomes half, then what will be increase in rate of reaction if concentration of B is doubled ?
35. For which type of reaction the order of reaction and molecularity are same?
36. The value of rate constant for a reaction is 2.75 sec–1, then the order of reaction is:
37. For reaction 2SO2(g) + O2(g) Products,
if pressure of gaseous components is increased by three times then reaction rate:
38. In the reaction A β†’ B if the concentration of A is doubled then the reaction rate increases by 1.59 times then what will be the order of reaction?
39. The value of rate constant for the reaction
A + B β†’ Product is 1.25 Γ— 10-2 sec-1. if the concentration of A is doubled the reaction rate increases by two times, then what will be increase in rate of reaction if the concentration of B is increased by four times?
40. Units of rate constant of first and zero order reactions in terms of molarity M unit are respectively:
41. The reaction 2A + B + C β†’ D + E is found to be first order in A, second order in B and zero order in C. What is the effect on the rate of increasing concentration of A, B and C two times?
42. The rate of the reaction
CCl3CHO + NO β†’ CHCl3 + NO + CO is equal to rate k[CCl3CHO][NO]. If concentration is expressed in mol/L. The unit of k is:
43. The unit of rate constant of a third order chemical reaction is:
44. The rate law for a reaction between the substances A and B is given by rate = k[A]n [B]m. On doubling the concentration of A and halving the concentration of B, the ratio of the new rate to the earlier rate of the reaction will be as:
45. For the reaction H2(g) + Br2(g) β†’ 2HBr(g). The experimental data suggest rate = k[H2][Br2]1/2. The molecularity and order of the reaction are respectively:
46. The following mechanism has been proposed for the reaction of NO with Br2 to form NOBr2 (NO(g) + Br2(g)  NOBr2(g))
NOBr2(g) + NO(g) β†’ 2NOBr(g)
If the second step is the rate determining step, the order of the reaction with respect to NO(g) is:
47. A reaction involving two different reactants can never be:
48. The burning of coal represented by the equation; C(s) + O2(g) β†’ CO2(g). The rate of this reaction is increased by:
49. Which of the following statement is incorrect about the molecularity of a reaction?
50. For a reaction A + B β†’ Products, the rate of the reaction was doubled. When the concentration of A and B were doubled, the rate was again doubled, the order of the reaction with respect to A and B are:
51. For the reaction A β†’ B, the rate expression is r = k[A]n. When the concentration of A is doubled, the rate of reaction is quadrupled. The value of n is:
52. For a chemical reaction, ______ can never be a fractional.
53. If the rate of reaction A β†’ B doubles on increasing the concentration of A by 4 times, the order of the reaction is:
54. The rate constant for a chemical reaction has units L mol–1s–1, order of the reaction will be:
55. Which statement about molecularity of a reaction is wrong?
56. If the volume of the vessel in which the reaction 2NO + O2 β†’ 2NO2 is occurring is diminished to 1/3rd of its initial volume. The rate of the reaction will be increased by:
57. For a reaction A + B β†’ C + D, if the concentration of A is doubled without altering the concentration of B, the rate gets doubled. If the concentration of B is increased by nine times without altering the concentration of A, the rate gets tripled. The order of the reaction is:
58. For the reaction, 2N2O5(g) β†’ 4NO2(g) + O2(g)
If the concentration of NO2 increase by
5.2 Γ— 10–3 M in 100 s then the rate of the reactions:
59. The rate of the reaction A β†’ product, at the initial concentration of 3.24 Γ— 10–2 M is nine times its rate at another initial concentration of 1.2 Γ— 10–3 M. The order of the reaction is:
60. Consider the reaction 2A + B β†’ product
When concentration of B alone was doubled, the half-life did not change. When the concentration of A alone was doubled, the rate increased by two times. The unit of rate constant for this reaction is:
61. The rate of reaction between two reactants A and B decreases by a factor 4, if the concentration of reactant B is doubled, than the order of this reaction with respect
to B i:
62. Rate of reaction can be expressed by following rate expression, rate = k[A]2[B].
If concentration of A is increased by 3 times and concentration of B is increased by 2 times, how many times rate of reaction increases?
63. The data for the reaction, A + B β†’ C;
The rate law corresponds to the above data is:
64. In a reaction, when the concentration of reactant is increased two times, the increase in rate of reaction was four times. Order of reaction is:
65. For a reaction A + 2B β†’ C, rate is given by
r = k[A][B]2. The order of reaction is:
66. During the kinetic study of the reaction
2A + B β†’ C + D following results were obtained.
On the basis of above data which one is correct:
67. For the reaction A β†’ B, when concentration of A is made 1.5 times, the rate of reaction becomes 1.837 times. The order of reaction is
68. A reaction involving A, B and C as reactants is found to obey the rate law, rate = k[A]x[B]y[C]z. When the concentration of A, B and C are doubled separately, the rate is also found to increase two, zero and four times respectively. The overall order of the reaction is
69. In a chemical reaction two reactants take part. The rate of reaction is directly proportional to the concentration of one of them and inversely proportional to the concentration of the other. The order of reaction is:
70. _________ of a reaction cannot be determined experimentally.
71. What is the order of a reaction which has an expression rate = k[A]3/2[B]–1?
72. The rate of elementary reaction A β†’ B increases by 100 times when the concentration of A is increased ten folds. The order of the reaction with respect to A is:
73. The order of a gaseous phase reaction for which rate becomes half if volume of container having same amount of reactant is doubled is:
74. Consider a reaction; aG + bH β†’ Products
When concentration of both the reactants G and H is doubled, the rate increases by eight times. However, when concentration of G is doubled keeping the concentration of H fixed, the rate is doubled. The overall order of the reaction is:
75. In a reaction, the rate expression is,
rate = K[A][B]2/3[C]0, the order of reaction is:
76. Which one of the following statements for the order of a reaction is incorrect?
77. If the rate of reaction between A and B is given by, rate = K[A][B]n, then the reaction is:
78. In a reaction, A + B β†’ Product, rate is doubled when the concentration of B is doubled, and rate increases by a factor of
8 when the concentrations of both the reactants
(A and B) are doubled, rate law for the reaction can be written as:
79. For a reaction between gaseous compounds,
2A + B β†’ C + D
The reaction rate = k[A][B]. If the volume of the container is made of the initial, then what will be the rate of reaction as compared to the initial rate?
80. In a reaction A + B β†’ C, the rate expression is R = k[A][B]2. If the concentration of both the reaction is doubled at constant volume then the rate of the reaction will be:
81. For the reaction, 2A + B β†’ products, the active mass of B is kept constant, and that of A is doubled. The rate of reaction will be then;
82. For the fourth order reaction, what is the unit of k?
83. For the reaction; 2N2O5 β†’ 4NO2 + O2, rate and rate constant are 1.02 Γ— 10–4 M sec–1 and
3.4 Γ— 10–5 sec–1 respectively, then concentration of N2O5, at that time will be:
84. The rate of the elementary reaction,
2NO + O2 β†’ 2NO2, when the volume of the reaction vessel is doubled:
85. If the concentration of reactants is increased by 'x' then rate constant k becomes.
86. The reaction X β†’ product, follows first order kinetics. In 40 minutes, the concentration of X changes from 0.1 M to 0.025 M, then the rate of reaction when concentration of X is
0.01 M is:
87. For first order reaction, = _____?
88. Mention the value of slope in the graph of rate of reaction versus time for zero order reactions.
89. By which formula the value of can be found out for the first order reaction, where k = Rate Constant.
90. In the first order reaction R β†’ P if the initial concentration of reactant is [R]0, then what would be the concentration of the reactant left after time ?
91. For the first order reaction what would be the value of Y, if t96% Γ· ty% = 2?
92. What is the formula to find value of t1/2 for a zero order reaction?
93. For a first order reaction the graph log
[A] versus t is given below:
x is equal to
94. The rate constant of a first order reaction is 4 Γ— 10–3sec–1. At a reactant concentration of 0.02 M, the rate of reaction would be:
95. The rate of first order reaction, A β†’ Products, is 7.5 Γ— 10–4mol litre–1sec–1. If the concentration of A is 0.5 mol litre–1. The rate constant is:
96. Half-life period of a first order reaction is 1386 seconds. The specific rate constant of the reaction is:
97. Which is correct about zero order reaction?
98. Consider the following statements, the rate law for the acid catalysed hydrolysis of an ester being given as: Rate = k[H+][ester] = k' [ester].
If the acid concentration is doubled at constant ester concentration:
I. The second order rate constant, k is doubled.
II. The pseudo first order rate constant, k is double.
III. The rate of the reaction is doubled. Which of the above statements are correct?
99. Half-life of two samples is 0.1 and 0.8 s. Their respective concentration is 400 and 50 respectively. The order of reaction is:
100. A reaction proceeds by first order, 75% of this reaction was completed in 32 min. The time required for 50% completion is:
101. The half-life period of a first order reaction is 1 min 40 s. Calculate its rate constant.
102. The halftime of a second order reaction is:
103. Acid hydrolysis of sucrose is:
104. Mathematical expression for t1/4 i.e., when (1/4)th reaction is over following first order kinetics can be given by:
105. The rate of first order reaction is
1.5 Γ— 10–2 mol L–1 min–1 at 0.5 M concentration of the reactant. The half-life of reaction is:
106. Which one is not correct?
107. In a first order reaction, the concentration of the reactant is decreased from 1.0 M to 0.25 M in 20 minute. The rate constant of the reaction would be:
108. In the reaction,
2N2O5 β†’ 4NO2 + O2 initial pressure is
500 atm and rate constant k is 3.38 Γ— 10–5s–1 after 10 min the final pressure of N2O5 is:
109. Half-life of a reaction is found to be inversely proportional to the cube of initial concentration. The order of reaction is:
110. For a zero order reaction:
111. The rate constant for the first order reaction is 60 s–1. How much time will it take to reduce the concentration of the reaction to
1/16 M value?
112. The unit and value of rate constant and that of rate of reaction are same for.
113. The time taken for the completion of 3/4 of a first order reaction is:
114. A zero order reaction is one:
115. For zero order reaction, the integrated rate equation is:
116. The half-life period of a first order reaction is 69.3 s. What is the rate constant?
117. A reactiotn has a rate constant of 0.5 mol–1 dmΒ³ min–1. If initial concentration of the reactant is 0.2 mol dm–3, half-life of the reaction is:
118. A first order reaction is 20% complete in 10 min. What is the rate constant of the reaction?
119. The rate constant of a zero order reaction is 0.2 mol dm–3 h–1. If the concentration of the reactant after 30 min is 0.05 mol dm–3. Then its initial concentration would be:
120. For a reaction, x(g) β†’ y(g) + z(g) the half-life period is 10 min. in what period of time would the concentration of X be reduce to 10% of original concentration?
121. For the first order reaction with the rate constant k, which expression gives the rate half-life period? (Initial conc. = a)
122. For a given reaction of first order, it takes
15 minute for the concentration to drop from 0.8 M litre–1 to 0.4 M litre–1. The time required for the concentration to drop from 0.1 M litre–1 to 0.025 M litre–1 will be:
123. At 500K, the half-life period of a gaseous reaction at an initial pressure of 80 kPa is
350 s. When the pressure is 40 kPa, the
half-life period is 175 s. The order of the reaction is:
124. The half-life period for zero order reaction
A β†’ product, is 100 min. How long will it take in 80% completion?
125. In a first order reaction the concentration of reactant decreases form 800 mol/dm6 to
50 mol/dm6 in 2 Γ— 104 s. The rate constant of reaction in s–1 is:
126. The rate constant of a first order reaction whose half-life is 480 s is:
127. 2A β†’ B + C; it would be a zero order
reaction when:
128. The plot between concentration versus time for zero order reaction is represented by:
129. In the first order reaction, the concentration of the reactants is reduced to 25% in one hour. The half-life period of the reaction is:
130. For a first order reaction, the initial concentration of a reactant is 0.05 M. After 45 min it is decreased by 0.015 M. Calculate half reaction time ().
131. In the reaction A + B β†’ products, if B is taken in excess, then it is an example of.
132. The ratio of the times for 99.9% of the reaction to complete and half of the reaction to complete is:
133. After how many second will the concentration of the reactant in a first order reaction be halved if the rate constant is 1.155 Γ— 10–3 s–1?
134. The inversion of cane sugar into glucose and fructose is:
135. What is the two third life of a first order reaction having k = 5.48 Γ— 10–14 s–1?
136. Order of radioactive disintegration reaction is:
137. The rate constant of a first order reaction is
6.9 Γ— 10–3 s–1. How much time will it take
to reduce the initial concentration to its
1/8th value?
138. The of the first order reaction is.
139. The time required for 100% completion of a zero order reaction is.
140. The thermal decomposition of a compound is of first order. If a sample of the compound decompose 50% in 120 min, then, what time will it take to undergo 90% decomposition?
141. For a first order reaction, A β†’ products, the rate of reaction at [A] = 0.2 M is 1.0 Γ— 10–2 mol L–1 min–1. The half-life period for the reaction is:
142. For a first order reaction k = 100 s–1. The time for completion of 50% reaction is:
143. The rate constant for a first order reaction whose half-life is 480 s is:
144. For a reaction, the rate constant is 2.34 s–1. The half-life period for reaction is:
145. In a first order reaction A β†’ B, if k is the rate constant initial concentration of the reactant is 0.5 M, then half-life is:
146. DDT on exposure to water decomposes.
Half-life is 10 year. How much time it will take for its decomposition to 99%?
147. A first order reaction is 20% complete in 10 min. Calculate the time for 75% completion of the reaction.
148. The half-life period of a first order chemical reaction is 6.93 min. The time required for the completion of 99% of the chemical reaction will be: (log2 = 0.302)
149. A first order reaction has a rate constant 1.15 Γ— 10–3 s–1. How long will 5g of this reactant take to reduce to 3 g?
150. For the reaction,
A + 2B β†’ Product.
The rate law is given by = K[A]2β‹…[B].
If A is taken in large excess, the order of the reaction will be:
151. If rate of reaction doubles on increasing temperature by 10Β°C, then how many times the rate of reaction will be increased
if temperature of reaction increases to 50Β°C?
152. Which of the following is the correct relation for endothermic reaction?
153. Activation energy of a reaction is:
154. The activation energy for a reaction is
9.0 kcal/mol. The increase in the rate constant when its temperature is increased from
298K to 308K is:
155. In Arrhenius plot intercept is equal to.
156. The activation energy of a reaction is zero. The rate constant for the reaction.
157. According to the Arrhenius equation a straight line is to be obtained by plotting the logarithm of the rate constant of a chemical reaction (logk) against:
158. In respect of the equation k = Ae–Ea/RT in chemical kinetics, which one of the statement is correct?
159. Effect of temperature on reaction rate is
given by:
160. An endothermic reaction A β†’ B has an activation energy of 15 kcal/mol and the energy of reaction is 5 kcal/mol. The activation energy for the reaction B β†’ A is:
161. The Arrhenius equation expressing the effect of temperature on the rate constant of reaction is:
162. The rate constant of a reaction at temperature 200K is 10 times less than the rate constant at 400K. What is the activation energy (Ea) of the reaction?
163. Activation energy of a chemical reaction can be determined by:
164. The rate constants k1 and k2 for two different reactions are 1016 e–2000/T and 1015 e–1000/T, respectively. The temperature at which k1 = k2 is:
165. The activation energy of exothermic reaction A β†’ B 80 kJ mol–1. The heat of reaction is 200 kJmol–1. The activation energy for the reaction B β†’ A(in kJ mol–1) will be:
166. Temperature coefficient of a reaction is 2. When temperature is increased from 30Β°C to 100Β°C, rate of the reaction increases by:
167. The slope in Arrhenius plot, is equal to.
168. A first order reaction is 50% complete in 30 min at 27Β°C and in 10 min at 47Β°C. The energy of activation of the reaction is.
169. What is the activation energy for the decomposition of N2O5 as,
N2O5  2NO2 + O2,
if the values of rate constant = 3.45 Γ— 10–5 at 27Β°C and rate constant = 6.9 Γ— 10–3 at 67Β°C?
170. The rate constant of a reaction increases by 5% when its temperature is raised from
27Β°C to 28Β°C. The activation energy of the reaction is
171. Temperature dependent equation can be written as:
172. When a graph is plotted between lnk and 1/T for a first order reaction, a straight line is obtained. The slope of the line is equal to:
173. For the two gaseous reactions, following data are given;
A β†’ B; k1 = 1010 e–20,000/T,
C β†’ D; k2 = 1012 e–24,606/T.
The temperature at which k1 becomes equal to k2 is:
174. For a first order reaction A β†’ P, the temperature (T) dependent rate constant (k) was found to follow the equation.
logk = –(2000)/T + 6.0
The pre-exponential factor A and the activation energy Ea, respectively, are:
175. In Arrhenius equation k = Ae–Ea/RT, the quantity – Ea/RT is referred as:
176. The rate of a chemical reaction doubled for every 10Β°C rise in temperature. If the temperature is increased by 80Β°C the rate of reaction increases by:
177. The rate constant of a reaction is given by
k = 2.1 Γ— 1010 exp(–2700/RT). It means that,
178. The activation energy of a reaction at a given temperature is found to be 2.303 RT J mol–1. The ratio of rate constant to the Arrhenius factor is:
179. Chemical reactions with very high Ea values are generally:
180. The rate constant is doubled when temperature increases from 27Β°C to 37Β°C. Activation energy in kJ is
181. Effective collisions are those in which molecules must:
182. In a reaction, the threshold energy is equal to:
183. Collision theory is applicable to:
184. For producing the effective collisions the colliding molecules must have:
185. According to collision theory of reaction rates:
186. The minimum energy required for the reacting molecules to undergo reaction is:
187. Increase in the concentration of the reactants leads to the change in:
188. Which of the following theory is not related to chemical kinetics?
189. The minimum energy required for a molecule to take part in a reaction is called
190. Assertion : The rate of chemical reaction increases in the presence of catalyst.
Reason : Catalyst lowers the activation energy of the reactants.
191. Assertion : The hydrolysis of ethyl acetate with aqueous HCI is a pseudo first-order process.
Reason : HCl acts as a catalyst in the hydrolysis reaction.
192. Assertion : Mixing an aqueous solution of silver nitrate and sodium chloride immediately precipitates silver chloride.
Reason : Ionic reaction are very fast.
193. Assertion : For a first order reaction, is dependent on the rate constant.
Reason : For a first order process, ∝ [R]0.
194. Assertion : Rate of a reaction is the change in concentration
of reactant or product per unit time.
Reason : Rate of reaction remains constant throughout the reaction.
195. Assertion : All collisions of molecules lead to the formation of products.
Reason : Reactant molecules do not undergo chemical change regardless of every collision.
196. Assertion : The rate of a reaction never depends on the concentration.
Reason : Lower the activation energy, faster the reaction.
197. Assertion : Not more than three molecularities are found.
Reason : The overall molecularity of a complex process is equal to the molecularity of the slowest step.
198. Assertion : For reaction CHCl3 + Cl2 β†’ CCl4 + HCl, Rate = k[CHCl3] [Cl2].
Reason : The rate of a reaction is always equal to the sum of the stoichiometric coefficients of the reacting species in a balanced chemical equation.
199. Assertion : Following reaction is first order reaction.
C12H22O11 + H2O C6H12O6 + C6H12O6
Sucrose Glucose Fructose
Reason : Change in concentration of H2O is negated.
200. Assertion : A catalyst increases the rate of a reaction without causing any permanent chemical change.
Reason : A catalyst changes the free energy of a reaction and the equilibrium constant of the reaction.
201. Assertion : A complex reaction takes place in different steps and the slowest step determines the rate of the reaction .
Reason : Order of reaction and molecularity are always the same .
202. Assertion : With respect to any reaction, the order of reaction can be zero, positive, or fractional.
Reason : Increase in concentration of reactants or products does not decrease the rate of the reaction.
203. Assertion : 10Β°C in temperature increases For a chemical reaction rate constant become almost doubles.
Reason : t + 10Β°C, the fraction of molecules with energies equal to or greater than the activation energy doubles.
204. Assertion : The decomposition of gaseous ammonia on a hot platinum surface is a zero order reaction at high pressure.
Reason : For a zero order reaction , the rate of the reaction is independent of the initial concentration.
205. Assertion : In a reversible endothermic reaction the Ea of the forward reaction is greater than that of the backward reaction.
Reason : Increasing the temperature of a substance increases the fraction of molecules, which collide with energy greater than Ea.
206. Assertion : In a zero order reaction, if concentration of the reactant is doubled, half life period is also doubled.
Reason : Rate of reaction of zero order reaction is independent from concentration of the reactants.
207. Use the appropriate symbols T (True) and
F (False) for the following statements regarding chemical equilibrium.
(i) Concentration of reactant and product are constant.
(ii) Rate of forward and backward reaction are same.
(iii) The reaction is moving fast.
(iv) Factors like pressures and temperature are constant.
208. Select the correct option using T (True) or F (False) symbol for the following statements regarding Elementary reaction:
(i) It is a multi-step reaction.
(ii) Its rate constant is very small.
(iii) It has the same molecularity and order of reaction.
(iv) It is always endothermic . So it is a high temperature reaction .
209. Select the correct option using T for (True)statements and F for (False) statements given below.
(i) Molecularity means the sum of
mole-numbers of reactants in a balanced process.
(ii) Molecularity means number of molecules associated with slow step of the reaction.
(iii) Molecularity means order of reaction.
(iv) Molecularity can be defined only for elementary reaction.
210. Choose the correct option using T (True) and F (False) notation for the following statements:
(i) Rate = = k [A] [B] [C] Is rate equation for initial reaction.
(ii) Ionic reactions are instantaneous.
(iii) The unit of rate of reaction varies with the order of the reaction.
(iv) Every first order process is unimolecular.
211. Choose T (True) or F (False) for the following statements.
(i) Molecularity can be fractional.
(ii) Molecularity and order can be 0, 1,2 and 3.
(iii) For a gaseous reaction the rate of reaction depends on the pressure of reactant or product.
(iv) Integral rate equation is more practical than differential rate equation for determining rate of reaction.
212. Choose T (True) or F (False) for the following statements.
(i) Molecularity is a theoretical derivation, while order of reaction is practical derivation.
(ii) The value of molecularity is a positive integer, while the value of order of reaction can be positive, negative or zero.
(iii) The molecularity explains the methodology of the reaction , whereas the order does not provide any information about the methodology.
(iv) Order of reaction and molecularity are same for elementary reaction.
213. Choose T (True) or F (False) for the following statements depending on the order of reaction.
(i) The molecularity of a second order reaction can be two.
(ii) The value of the order of reaction can be positive, zero, negative or fractional and is determined experimentally.
(iii) Reaction of higher order are rare.
(iv) The order of reaction increases with increasing temperature.
214. Choose T (True) or F (False) for the following statements related to the order of reaction:
(i) Order of reaction increases with increasing temperature.
(ii) Higher order of reaction are rare.
(iii) The order of reaction depends on the concentration of the product.
(iv) The overall reaction order of
H
2 + Br2 β†’ 2HBr is 2.
215. For the reaction A2(g) + 3B2(g) β†’ 2AB3(g) use notation T or F depending on the statements given below. (Molecular weight of A = 14, Molecular weight of B = 1)
(i) When 7 g of A is used 17 g of AB3 is produced.
(ii) when 28 g of A is used 34 g of AB3 is produced.
(iii) – = +
(iv) – 2 = +
216. Choose the correct option using T (True) and F (False) notation for the following statements.
(i) The cooking time of rice in a closed pressure cooker on a mountain top or at sea level is the same at both places.
(ii) Bornvita powder dissolves faster in milk than frozen Bornvita pieces.
(iii) Catalysts reduce the amount of energy that has to be supplied externally to the reaction.
(iv) The rate of reaction is same whether the reactant is in liquid state or gas state.
217. Determine the statements True (T) and
False (F), for the first order reaction,
2N2O5 β†’ 4NO2 + O2.
(i) The concentration of the reactant decreases exponentially with time.
(ii) Both the half-time of the reaction decreases with increasing temperature.
(iii) The half-time of the reaction depends on the initial concentration of the reactant.
(iv) The reaction proceeds to 99.6% completion in eight half-life duration.
218. Determine the True (T) and False (F) statements from the relationship between the rate of consumption of A and the rate of production of B for the reaction A β†’ 2B.
(i) – = (ii) – =
(iii) – = (iv)–=
219. When can nitrogen and oxygen combine? Determine the True (T) and False (F) statements for it.
(i) A collision between N2 and O2 must occur.
(ii) The molecules do not need to have maximum total activation energy.
(iii) The molecules must have a minimum amount of kinetic energy.
(iv) The molecules must have the proper orientation.
220. The rate equation for the reaction 2A + B β†’ C is found to be: rate = k [A] [B] determine the statements True (T) and False (F).
(i) The value of k is independent of the concentrations of A and B.
(ii) Unit time of k is sec–1.
(iii) The half-life time of the reaction is constant.
(iv) The rate of production of B is twice the rate of consumption of A.
Class 12 Chemistry (Part 1) 014

Time (sec)

0

100

200

300

Pressure (Pa)

4 Γ— 103

3.5 Γ— 103

3 Γ— 103

2.5 Γ— 103

Exp.

[A]0

[B]0

Initial rate

1

0.012

0.035

0.10

2

0.024

0.070

0.80

3

0.024

0.035

0.10

4

0.012

0.070

0.80

Exp.

[A] in

M

[B] in

M

Initial rate of

formation

D in M s–1

I

0.1

0.1

6.0 Γ— 10–3

II

0.3

0.2

7.2 Γ— 10–2

III

0.3

0.4

2.88 Γ— 10–1

IV

0.4

0.1

2.40 Γ— 10–2

Options

  1. (A) TFFF
  2. (B) TFTF
  3. (C) TTFF
  4. (D) FTTT

Answer

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#83 CS πŸ–Ό 17

Question

Rate of reaction relates to the concentration of reactants and products changing per unit time. β€œRate of a reaction is the change in concentration of reactants or products per unit time,”
Rate =
Average Rate: Average rate is taken as the ratio of change in total concentration to total time taken.
Average Rate =
Instantaneous Rate: The instantaneous rate of a reaction is the rate at a specific time. The instantaneous rate of a reaction is the ratio of the change in concentration over a number of small time periods.
Instantaneous Rate =
(a) For the following reaction rate of appearance of I2 is 1.14 Γ— 10–2. Then find out rate of disappearance of MnO–4.
2MnO–4 + 10I– + 16H+ β†’ 2Mn2+ + 5I2 + 8H2O
(b) In kinetic study of a chemical reaction, slopes are drawn at different times in the plot of concentration of reactants versus time. The magnitude of slopes with increase of time.
(c) 2NO(g) + O2(g) β†’ 2NO2(g); If = 0.052 Ms–1 then, = _________.
(d) In the reaction 2A + B β†’ A2 reactant B will disappear _________.

Answer

(a) 4.56 Γ— 10–3 Ms–1
2MnO–4 + 10I– + 16H+ β†’ 2Mn2+ + 5I2 + 8H2O
– = +
= Γ— (1.14 Γ— 10–2)
= 4.56 Γ— 10–3 m/sec
(b) Decrease
As the reaction progresses, the concentration of reactants decrease. So, the rate of reaction slow down over time.
Therefore, the magnitude of slops decrease with the increase of time.
(c) 0.026 Ms–1
– = – = +
= Γ— 0.052 β‡’ 0.026 m/sec
(d) At half-life the disappearance of rate of A
2A + B β†’ A2
– = –
Reactant B will disappear half as fast as reactant A.
#84 CS πŸ–Ό 2

Question

In Arrhenius equation K = A, Ea is activation energy.
According to the collision theory, a reaction occurs only when reactant molecules come close and collide with each other at the same time. During the collisions rearrangement of atoms takes place leading to the formation of products. The rearrangement of an atom involves the breaking of a bond and the formation of a new bond. Molecules rearrangements can only occur when the colliding molecules have energy equal to or greater than the minimum energy required for rearrangement. If the atom/molecule do not have this minimum energy, no rearrangement of molecules will occur and no product will be formed. The difference between the minimum energy required to rearrange molecule and the average energy of the reaction is called the activation energy (Ea). That is, the additional energy of a reactant molecule over and above the energy it already possesses to bring about a chemical change is called activation energy.
(a) Collision frequency is _________ .
(b) For the process R β†’ P the potential energy versus reaction axis is given. The enthalpy change of the reaction is ________ to energy corresponding.
(c) Activation energy required for a reaction can be reduced by what?
(d) Which of the following statements is not true?
(A) For an endothermic reaction, the heat of reaction is less than the activation energy.
(B) For an exothermic reaction, the heat of reaction is greater than the activation energy.
(C) For an exothermic reaction, the activation energy of the forward reaction is lower than that of the backward reaction.
(D) For an endothermic process, the activation energy of the forward reaction is higher than that of the backward reaction.

Answer

(a) Collision frequency (Z)Β is defined as theΒ total number of collisions that occur per unit volume per unit timeΒ in a reaction mixture.
(b) b – a
Since the product energy (b) is lower than the reactant energy (a) in this specific graph, the reaction isΒ exothermic, andΒ Ξ”HΒ would be negative.
The enthalpy change corresponds to the valueΒ (bβˆ’a).
(c) Adding of catalyst
The activation energy required for a reaction can be reduced byΒ adding a catalyst.
(d) (B) For an exothermic reaction, the heat of reaction is greater than the activation energy.
For an exothermic reaction, the heat of reaction (Ξ”H) is the difference between reactants and products.Β It is not inherently greater than the activation energy.
#85 CS πŸ–Ό 6

Question

A pharmaceutical company is studying how the rate of drug decomposition changes with temperature. The drug breaks down following first order kinetics. At different temperatures, the following rate constants were measured:

Temperature (0Β°C)

Rate Constant k(s–1)

25Β°C

3.0 Γ— 10–4

35Β°C

8.1 Γ— 10–4

The drug must remain stable during storage, so scientist want to predict:
The activation energy (Ea) using the Arrhenius equation.
The half-life of the drug at 25Β°C.
Whether the drug decomposes significantly in 6 hours.
How increasing temperature affects shelf life.
(R = 8.314 J mol–1 K–1).
(a) Using the Arrhenius equation, calculate the activation energy (Ea).
(b) Calculate the half-life (t1/2) of the drug at 25Β°C.
(c) What fractions of the drug will remain after 6 hours at 25Β°C?
(d) Explain how an increase from 25Β°C to 35Β°C affects the drug's shelf life.

Answer

(a) Arrhenius equation
ln = =
k1 = 3.0 Γ— 10–4 T1 = 298 K
k2 = 8.1 Γ— 10–4 T2 = 308 K
∴ ln (2.7) =
∴ 0.993 = (0.000109)
∴ Ea =
= 75.8 kJ / mol
(b) t1/2 = =
= 2310 second
= 38.5 minutes
(c) Fraction remaining after 6 hours
First - order: N = Noe–kt (t = 21600 sec)
N = e–(3 Γ— 10–4) (21600)
N = e–6.48
= 0.015
= 0.15%
(d) Rate increases from 3 Γ— 10–4 to 8.1 Γ— 10–4 (Almost 2.7 times).
#86 CS πŸ–Ό 5

Question

Higher temperature accelerates decomposition, reducing shelf life drastically.
A chemical industry studies the decomposition of N2O5, which follows first order kinetics:
2N2O5 β†’ 4NO2 + O2
At 25Β°C, the rate constant is 6.5 Γ— 10–3s–1.
Samples show the following data:
Initial concentration: 0.50 M
After t seconds, conc. reduces to 0.10 M
The industry aims to determine:
1. Time required to reach 0.10 M.
2. Total gas evolved.
3. Whether the reaction is feasible at low temperatures.
4. Importance of first order kinetics in industrial reactors.
(a) Calculate the time required for concentration to fall from 0.50 M to 0.10 M.
(b) How many moles of O2 are formed from 0.50 mol of N2O5?
(c) If temperature decrease, what happens to the rate constant?
(d) State one industrial advantage of first order reactions.

Answer

(a) t = ln
= ln
= 153.8 (1.609)
t = 247.5 seconds.
(b) 2 mole N2O5 β†’ 1 mol O2
∴ 0.50 mole N2O5 β†’ 0.25 mole O2
(c) Temp ↓ β†’ Rate constant decreases exponentially (Arrhenius eq.)
Reaction slow down drastically.
(d) The half-life of first order reaction is independent of the initial reactant concentration. So, it is easy to control and predictable.
Reaction Rate: Change in concentration of reactants or products per unit time.
Average Rate: Rate calculated over a long-time interval from overall concentration change.
Instantaneous Rate: Rate at a specific moment, obtained from the slope of tangent on a concentration–time curve.
Rate Law: Experimentally derived expression relating rate to reactant concentrations.
Rate Constant (k): Proportionality constant in the rate law; depends on temperature and catalyst.
Order of Reaction: Sum of powers of concentration terms appearing in the rate law.
Molecularity: Number of species colliding in a single elementary step to form products.
Zero-Order Reaction: Reaction whose rate is independent of reactant concentration.
First-Order Reaction: Reaction whose rate is proportional to the first power of one reactant.
Half-Life (tΒ½): Time required for the concentration of a reactant to become half of its initial value.
Pseudo First-Order Reaction: Higher-order reaction that behaves like first order because one reactant is in excess.
Activation Energy (Ea): Minimum energy required for reactants to form the activated complex.
Activated Complex / Transition State: High-energy, unstable intermediate formed during reaction progression.
Arrhenius Equation: Equation relating rate constant (k) with temperature and activation energy.
Collision Theory: Reaction occurs only when molecules collide with sufficient energy and correct orientation.
Steric Factor (P): Fraction of collisions with the proper orientation to form products.
Reaction Coordinate: Path showing energy changes as reactants convert into products.
Rate-Determining Step: Slowest step in a multi-step mechanism controlling total reaction rate.
Exothermic Reaction: Reaction releasing heat where products have lower energy than reactants (Ξ”H < 0).
Endothermic Reaction: Reaction absorbing heat where products have higher energy than reactants (Ξ”H > 0).

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