Chapter Wise CBSE-Board Sample Paper-Chemical Kinetics - KEY
Chapter Wise CBSE-Board Sample Paper-Chemical Kinetics - KEY
This equation is called Arrhenius equation. The constant ‘A’ is called Arrhenius constant (or) pre-
exponentional factor
Logarithm of equation (i) is given as
Ea
log10 K = log10 A -
2.303RT
The rate constant for a reaction is
1.25 x10 4
log10 K ( sec −1 ) =14 - k
T
The following questions are multiple choice questions. Choose the most appropriate answer:
i) The pre-exponential factor (or) frequency factor of the reaction under consideration is
a) 1.25 x 104 b) 10-14 c) 1014 d) 14
ii) At what temperature, rate constant of the reaction is equal to the pre exponential factor?
1.25 x10 4 14
a) T = 0 k b) T = ∞k c) T = k d) T = k
14 1.25 x10 4
iii) Energy of activation in kcal mol-1 is
a) 14 kcal mol-1 b) 57.2 kcal mol-1
14
c) 1.25 x 104 kcal mol-1 d) 4
kcal mol−1
1.25 x10
1
iv) The intercept of the plot of log10K against is equal to
T
Ea
a) log10A b) A c) d) Ea
2.303R
OR
1
The slope of the plot of log10K against is equal to
T
a) -28.6 x 102 b) -1.25 x 102 c) -1.25 x 104 d) -5 x 104
Following questions (No. 2 -5) are multiple choice questions carrying 1 mark each:
-d [ A ] 2 -d [ B ] 2 +d [ C ]
= k1 [ A ] ; = k 2 [A] ; = k 3 [ A ] the correct relation
2
2. For the reaction 2A → B + 3C; If
dt dt dt
between k1, k2 and K3 is
k1 k
a) k1 = k2 = k3 b) 2k1 = k2 = 3k3 c) 4k1 = k2 = 3k2 d) = k2 = 3
2 3
3. consider the plots, given below for the types of reaction nA → B + C
r1 = k[X]2
r2 = k[3X]2
r1 K [ X ]
2
=
r2 K [ 3X ]2
r1 1
⇒ = ⇒ r2 = 9r1
r2 9
0.693
=
480
= 0.00144 sec-1
K = 1.44 x 10-3 sec-1
14. A hypothetical reaction A2 + B2 → 2AB follows the mechanism as given below
K'
A2 ↽ ⇀ A + A (fast)
A + B2 → AB + B (slow)
A + B → AB (fast)
Find the order of overal reaction. (2)
Solution :
Rate equation is r = K[A] [B2] ------ (1)
'
K
A 2 ↽ ⇀ A + A (fast)
[ A ] ⇒ A 2 = K' A
2
'
K = [ ] [ 2]
[A2 ]
⇒ [ A ] = ( K' [ A 2 ] )
1
2
⇒ r = K ( K') [ A 2 ] [ B2 ]
1 1
2 2
r = K1 [ A 2 ] 2 [ B 2 ]
1
let KK' = K1
1
order of overall reaction = +1
2
3
=
2
15. A first order reaction has a rate constant 1.15 x 10-3 s-1. How long will 5g of this reactant take to reduce
to 3g? [log 5 = 0.699 and log 3 = 0.477] (2)
Solution :
K1 = 1.15 x 10-3 S-1
a = 5g and (a – x) = 3g
2.303 a
K1 = log
t (a − x)
2.303 5
1.15 x 10-3 = log
t 3
2.303
t= [ log5 - log3]
1.15 x10 -3
2NH3(g)
pt
→ N2(g) + 3H2(g)
-1 d [ NH 3 ] +d [ N 2 ] +1 d [ H 2 ]
∴ Rate = = = = 2.5 x10 4
2 dt dt 3 dt
d [ N2 ]
⇒ Rate of production of N2 = = 2.5 x10 -4 mol-1L S-1
dt
d [H 2 ]
Rate of production of H2 = = 3 x 2.5 x10 -4 mol-1LS-1
dt
SECTION C
Q.No 17 -21 are Short Answer Type II carrying 3 mark each.
17. The rate constants of a reaction at 500 K and 700 K are 0.02 S-1 and 0.07S-1 respectively. Calculate the
values of Ea and A. (3)
Solution :
T1 = 500 K; K1 = 0.02 S-1
T2 = 700 K; K2 = 0.07 S-1
K Ea T2 - T1
log 2 =
K1 2.303R T1T2
0.07 Ea 700-500
log =
0.02 2.303 x 8.314 700-500
7 Ea 200
log =
2 2.303 x 8.314 700 x 500
Ea 2
log 7 - log 2 =
19.1 3500
Ea 1
0.845 – 0.3010 =
19.1 1750
18186
⇒ log (0.02) = log A -
2.303 x 8.314 x 500
18186
⇒ log 2 x 10-2 = log A -
19.1x 500
18186
⇒ -1.7 + = log A
19.1x 500
⇒ -1.7 + 1.9 = log A ⇒ log A = 0.2
log A = log 1.6
⇒ A = 1.6
18. For a first order reaction show that time required for 99% completion is twice the time required for the
completion of 90% of reaction. (3)
Solution :
For a first order reaction
2.303 100
K= log
t99% (100 − 99 )
2.303 2.303 x 2
K= log10 2 ⇒ K =
t 99% t 99%
2.303 x 2
⇒ t 99% =
K
2.303 100
t 90% = log
K (100 − 90 )
2.303 100 2.303
t 90% = log ⇒ t 90% = log10
K 10 K
2.303
t 90% =
K
2.303
x2
t 99% K
= ⇒ t 99% = 2t 90%
t 90% 2.303
K
19. Calculate the half life of a first order reaction from their rate constants given below. (3)
i) 200S-1 ii) 2 min-1 iii) 4 years-1
Solution :
0.693
For a 1st order reaction t1/2 =
K
0.693
i) t 12 = = 0.346 x10-2
200 sec -1
t 1 2 = 3.46 x 10-3 sec
0.693
ii) t 12 = = 0.346 min
2min -1
0.693
iii) t 12 = = 0.173 years
4years -1
t 1 2 = 0.173 years
20. A reaction is first order in A and second order in B (3)
(i) Write the differential rate equation.
(ii) How is the rate affected on increasing the concentration of B three times?
(iii) How is the rate affected when the concentrations of both A and B are doubled.
Solution :
i) The differential rate equation is r = K[A] [B]2
ii) r1 = K[A] [B]2
r2 = K[A] [3B]2
r1 K [ A ][ B]
2
= ⇒ r2 = 9r1
r2 K [ A ] 9 [ B]2
∴ The rate of reaction will increase 9 times
iii) r1 = K[A] [B]2
r2 = K[2A] [2B]2 ⇒ r2 = K 2[A] 4[B]2
⇒ r2 = 8 K[A] [B]2
⇒ r2 = 8r1
∴ The rate of reaction will increase 8 times
21. The decomposition of A into product has value of k as 4.5 x 103 s-1 at 10°c and energy of activation 60
KJ mol-1. At what temperature would K be 1.5 x 104 s-1? (3)
Solution :
K1 = 4.5 x 103 S-1; K2 = 1.5 x 104 S-1
T1 = 10°C = 283 K; T2 = ?
Ea = 60 KJ / mol ⇒ Ea = 60 x 103 J/mol
K Ea 1 1
log 2 = -
K1 2.303R T1 T2
1.5 x104 60 x103 1 1
log = -
4.5 x103 2.303x 8.314 283 T2
10 60 x103 1 1
log = -
3 19.1 283 T2
19.1 1 1
(1 − log 3) 3
= -
60 x10 283 T2
19.1 1 1
[ 0.523] x 3
= -
60 x10 283 T2
1 1
0.166 x 10-3 = -
283 T2
1 1
= − - 0.166 x 10-3
T2 283
1
= 0.00353- 0.166 x10-3
T2
1
= 3.53 x10 -3 - 0.166 x10 -3
T2
1
= 3.364 x10 -3
T2
1
⇒T2 =
3.364 x10 -3
1000
T2 =
3.364
T2 = 297.2 K
SECTION D
Q.No 22 to 23 are long answer type carrying 5 marks each.
22. Nitrogen pentoxide decomposes according to equation (5)
2N2O5(g) → 4NO2(g) + O2(g)
This first order reaction was allowed to proceed at 40°C and the data below were collected.
[N2O5] M Time (min)
0.400 0.00
0.289 20.0
0.209 40.0
0.151 60.0
0.109 80.0
a) Calculate the rate constant. Include units with your answer.
b) What will be the concentration of N2O5 after 100 minutes?
c) Calculate the initial rate of reaction. [Given log 4 = 0.602; log 2.89 = 0.46, Antilog (0.706) = 5.08]
Solution :
a) [R]o = 0.400; [R]t = 0.289 at t = 20 min
2.303 [ R ]o
K= log
t [ R ]t
2.303 0.400 2.303 4
K= log = log
t 0.289 20 2.89
2.303
K= [log 4 − log 2.89]
20
2.303
= [ 0.602 − 0.46]
20
2.303
K= x 0.141
20
K = 1.625 x 10-2 min-1
b) At t = 100 min; [R]t = ?
2.303 0.4
K= log
100 [ R ]t
2.303 0.4
1.625 x 10-2 = log
100 [ R ]t
1.625 0.4 0.4
⇒ = log ⇒ 0.705 = log
2.303 [ R ]t [ R ]t
0.4
= Antilog(0.705)
[ R ]t
0.4 0.4
= 5.082 ⇒ [R]t =
[ R ]t 5.082
[ R ]t = 0.0787 M
c) Initial rate
i.e rate of reaction when t = 0
when t = 0 min; [R] = 0.400 M
Initial rate = K[R]
= 1.625 x 10-2 x 0.4
r = 6.500 x 10-3 mol L-1 min-1
23. For the hydrolysis of methyl acetate in aqueous solution, the following results were obtained. (5)
t1/2 0 30 60
[CH3COOCH3] mol L-1 0.60 0.30 0.15
i) Show that it follows pseudo first order reaction, as the concentration of water remains constant.
ii) Calculate the average rate of reaction between the time interval 30 to 60 seconds.
(Given log 2 = 0.3010, log 4 = 0.6021)
Solution :
2.303 [ R ]o
i) K = log
t [ R ]t
[R]o = 0.6 M; [R]t = 0.3 M and t = 30s
2.303 0.6
K= log
30 0.3
2.303 2.303
K= log 2 ⇒ K = x 0.3
30 30
K = 0.023 S-1
At t = 60 sec [R]t = 0.15
2.303 0.6 2.303
K= log ⇒K= log 4
60 0.15 60
2.303
K= x 0.6
60
K = 0.023 S-1
As the value of K is same in both the cases,
∴ Hydrolysis of methylacetate in aqueous solution follows pseudo first order reaction
-d [ CH 3COOH ]
ii) Average rate =
dt
-d [ 0.15- 0.30]
=
60 -30
0.15
=
30
Average rate = 0.005 MS-1