Chemical Kinetics

NEET Chemistry · 91 questions · Page 5 of 10 · Click an option or "Show Solution" to reveal answer

Q41
For the reaction A + B \to products, it is observed that (i) on doubling the initial concentration of A only, the rate of reaction is also doubled and (ii) on doubling the initial concentration of both A and B, there is a change by a factor of 8 in the rate of the reaction. The rate of this reaction is given by
A rate = k[A] 2 [B] 2
B rate = k[A] [B] 2
C rate = k[A] [B]
D rate = k[A] 2 [B]
Correct Answer
Option B
Solution

R = k[A] m [B] n ... (i) 2R = k[2A] m [B] n ... (ii) 8R = k[2A] m [2B] n ... (iii) from (i), (ii) and (iii), m = 1, n = 2 So, rate = k[A][B] 2

Q42
Half-life period of a first order reaction is 1386 seconds. The specific rate constant of the reaction is
A 0.5 × \times 10 -2 s -1
B 0.5 × \times 10 -3 s -1
C 5.0 × \times 10 -2 s -1
D 5.0 × \times 10 -3 s -1 .
Correct Answer
Option B
Solution

Specific rate constant k =

0.693t1/2{{0.693} \over {{t_{1/2}}}}

=

0.6931386{{0.693} \over {1386}}

= 0.5 ×\times 10 -3 sec -1

Q43
The rate constants k 1 and k 2 for two different reactions are 10 16 \cdot e -2000/T and 10 15 \cdot e -1000/T , respectively. The temperature at which k 1 = k 2 is
A 2000 K
B 10002.303K{{1000} \over {2.303}}K
C 1000 K
D 20002.303K{{2000} \over {2.303}}K
Correct Answer
Option B
Solution

k 1 = 10 16

e2000T{e^{ - {{2000} \over T}}}

k 2 = 10 15

e1000T{e^{ - {{1000} \over T}}}

On taking log of both the equations, we get

logk1=1620002.303T\log {k_1} = 16 - {{2000} \over {2.303T}}
logk2=1510002.303T\log {k_2} = 15 - {{1000} \over {2.303T}}

As k 1 = k 2

1620002.303T16 - {{2000} \over {2.303T}}

=

1510002.303T15 - {{1000} \over {2.303T}}

\Rightarrow T =

10002.303K{{1000} \over {2.303}}K
Q44
The reaction of hydrogen and iodine monochloride is given as : H 2(g) + 2ICl (g) \to 2HCl (g) + I 2(g) This reaction is of first order with respect to H 2(g) and ICl (g) , following mechanisms were proposed. Mechanism A : H 2(g) + 2ICl (g) \to 2HCl (g) + I 2(g) Mechanism B : H 2(g) + ICl (g) \to HCl (g) + HI (g) ; slow HI (g) + ICl (g) \to HCl (g) + I 2(g) ; fast Which of the above mechanism(s) can be consistent with the given information about the reaction?
A A and B both
B Neither A nor B
C A only
D B only
Correct Answer
Option D
Solution

The slow step is the rate determining step and it involves 1 molecule of H 2 (g) and 1 molecule of ICl(g) .

Hence the rate will be, r = k[H 2 (g)] [ICl(g)] \therefore The reaction is 1 st order with respect to H 2 (g) and ICl(g).

Q45
In a first-order reaction A \to B, if k is rate constant and initial concentration of the reactant A is 0.5 M, then the half-life is
A log2k{{\log 2} \over k}
B log2k0.5{{\log 2} \over {k\sqrt {0.5} }}
C ln2k{{\ln 2} \over k}
D 0.6930.5k{{0.693} \over {0.5k}}
Correct Answer
Option C
Solution

For first order reaction k =

2.303tlogaax{{2.303} \over t}\log {a \over {a - x}}

at

t1/2{t_{1/2}}

, x =

a2{a \over 2}
t1/2{t_{1/2}}

=

2.303klogaaa2{{2.303} \over k}\log {a \over {a - {a \over 2}}}

=

ln2k{{\ln 2} \over k}
Q46
If 60% of a first order reaction was completed in 60 minutes, 50% of the same reaction would be completed in approximately (log 4 = 0.60, log 5 = 0.69)
A 45 minutes
B 60 minutes
C 40 minutes
D 50 minutes
Correct Answer
Option A
Solution

For a first order reaction, k =

2.303tlogaax{{2.303} \over t}\log {a \over {a - x}}

k =

2.30360log10040{{2.303} \over {60}}\log {{100} \over {40}}

=

2.30360log2.5{{2.303} \over {60}}\log 2.5

= 0.0153 Also,

t1/2{t_{1/2}}

=

2.303klog10050{{2.303} \over k}\log {{100} \over {50}}

=

2.3030.0153log2{{2.303} \over {0.0153}}\log 2

= 45 min.

Q47
For the reaction, 2A + B \to 3C + D, which of the following does not express the reaction rate?
A d[A]2dt - {{d\left[ A \right]} \over {2dt}}
B d[C]3dt - {{d\left[ C \right]} \over {3dt}}
C d[B]dt - {{d\left[ B \right]} \over {dt}}
D d[D]dt {{d\left[ D \right]} \over {dt}}
Correct Answer
Option B
Solution

Given, 2A + B \to 3C + D Rate of reaction =

12d[A]dt=d[B]dt- {1 \over 2}{{d\left[ A \right]} \over {dt}} = - {{d\left[ B \right]} \over {dt}}

=

13d[C]dt=d[C]dt{1 \over 3}{{d\left[ C \right]} \over {dt}} = {{d\left[ C \right]} \over {dt}}
Q48
Consider the reaction : N 2(g) + 3H 2(g) \to 2NH 3(g) The equality relationship between d[NH3]dt{{d\left[ {N{H_3}} \right]} \over {dt}} and d[H2]dt - {{d\left[ {{H_2}} \right]} \over {dt}} is
A d[NH3]dt=d[H2]dt{{d\left[ {N{H_3}} \right]} \over {dt}} = - {{d\left[ {{H_2}} \right]} \over {dt}}
B d[NH3]dt=13d[H2]dt{{d\left[ {N{H_3}} \right]} \over {dt}} = - {1 \over 3}{{d\left[ {{H_2}} \right]} \over {dt}}
C +d[NH3]dt=23d[H2]dt + {{d\left[ {N{H_3}} \right]} \over {dt}} = - {2 \over 3}{{d\left[ {{H_2}} \right]} \over {dt}}
D +d[NH3]dt=32d[H2]dt + {{d\left[ {N{H_3}} \right]} \over {dt}} = - {3 \over 2}{{d\left[ {{H_2}} \right]} \over {dt}}
Correct Answer
Option C
Solution

N 2(g) + 3H 2(g) \to 2NH 3(g) Rate =

d[N2]dt=13d[H2]dt=12d[NH3]dt{{ - d\left[ {{N_2}} \right]} \over {dt}} = - {1 \over 3}{{d\left[ {{H_2}} \right]} \over {dt}} = {1 \over 2}{{d\left[ {N{H_3}} \right]} \over {dt}}

\Rightarrow

d[NH3]dt=23d[H2]dt{{d\left[ {N{H_3}} \right]} \over {dt}} = - {2 \over 3}{{d\left[ {{H_2}} \right]} \over {dt}}
Q49
For a first order reaction A \to B the reaction rate a reactant concentration of 0.01 M is found to be 2.0 × \times 10 -5 mol L -1 s -1 . The half-life period of the reaction is
A 30 s
B 220 s
C 300 s
D 347 s
Correct Answer
Option D
Solution

Given [A] = 0.01 M Rate = 2.0 × 10 –5 mol L –1 S –1 For a first order reaction Rate = k[A] k =

2×1050.01=2×103{{2 \times {{10}^{ - 5}}} \over {0.01}} = 2 \times {10^{ - 3}}

\Rightarrow

t1/2=0.6932×103=347sec{t_{1/2}} = {{0.693} \over {2 \times {{10}^{ - 3}}}} = 347\,\sec
Q50
The rate of reaction between two reactions A and B decreases by a factor of 4 if the concentration of reactant B is doubled. The order of this reaction with respect to reactant B is
A 2
B -2
C 1
D -1
Correct Answer
Option B
Solution

A + B \to Product Rate \propto [A] x [B] y .......(

1) The rate of the reaction decreases by a factor of 4 if the concentration of reactant B is doubled.

r4{r \over 4}

\propto [A] x [2B] y ......(2) From equation (1) and (2), we get

(12)y=4{\left( {{1 \over 2}} \right)^y} = 4

\Rightarrow y = -2 \therefore Order of this reaction with respect to reactant B is -2.

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