Chemical Kinetics

NEET Chemistry · 91 questions · Page 6 of 10 · Click an option or "Show Solution" to reveal answer

Q51
The rate of a first order reaction is 1.5 × \times 10 -2 mol L -1 min -1 at 0.5 M concentration of the reactant. The half-life of the reaction is
A 0.383 min
B 23.1 min
C 8.73 min
D 7.53 min
Correct Answer
Option B
Solution

For a first order reaction, A \to products Rate(r) = k[A] \Rightarrow k =

r[A]{r \over {\left[ A \right]}}

\Rightarrow k =

1.5×1020.5=3×102{{1.5 \times {{10}^{ - 2}}} \over {0.5}} = 3 \times {10^{ - 2}}

So,

t1/2=0.6933×102{t_{1/2}} = {{0.693} \over {3 \times {{10}^{ - 2}}}}

= 23.1 min

Q52
The temperature dependence of rate constant (k) of a chemical reaction is written in terms of Arrhenius equation, k=AeE/RTk = A \cdot {e^{ - E{}^ * /RT}}. Activation energy (E * ) of the reaction can be calculated by plotting
A kvsTk\,\,vs\,\,T
B kvs1logTk\,\,vs\,\,{1 \over {\log T}}
C logkvs1T\log \,k\,\,vs\,\,{1 \over T}
D logkvs1logT\log \,k\,\,vs\,{1 \over {\log T}}
Correct Answer
Option C
Solution

Arrhenius equation k =

AeEaRTA{e^{ - {{{E_a}} \over {RT}}}}

\Rightarrow log k = log A -

Ea2.303RT{{{{E_a}} \over {2.303RT}}}

Comparing it with equation of straight line i.e., y = mx + C On plotting log k vs

1T{1 \over T}

, we get a straight line, the slope indicates the value of activation energy.

Q53
If the rate of the reaction is equal to the rate constant, the order of the reaction is
A 0
B 1
C 2
D 3
Correct Answer
Option A
Solution

As r = k[A] n if n = 0 r = k[A] 0 or r = k thus for zero order reactions rate is equal to the rate constant.

Q54
The reaction A \to B follows first order kinetics. The time taken for 0.8 mole of A to produce 0.6 mole of B is 1 hour. What is the time taken for conversion of 0.9 mole of A to produce 0.675 mole of B?
A 1 hour
B 0.5 hour
C 0.25 hour
D 2 hours
Correct Answer
Option A
Solution

For first order reaction k =

2.303tlog[A]0[A]t{{2.303} \over t}\log {{{{\left[ A \right]}_0}} \over {{{\left[ A \right]}_t}}}

\Rightarrow k =

2.3031log0.80.2{{2.303} \over 1}\log {{0.8} \over {0.2}}

= 2.303 log 4 ....(

1) Let t 1 hour is required for changing the concentration of A from 0.9 mole to 0.675 mole of B.

Remaining mole of A = 0.9 – 0.675 = 0.225 \therefore k =

2.303t1log0.90.225{{2.303} \over {{t_1}}}\log {{0.9} \over {0.225}}

.....(2) From equation (1) and (2)

2.303t1log0.90.225{{2.303} \over {{t_1}}}\log {{0.9} \over {0.225}}

= 2.303 log 4 \Rightarrow

t1{{t_1}}

= 1 hr

Q55
The activation energy for a simple chemical reaction A \rightleftharpoons B is E aa in forward direction. The activation energy for reverse reaction
A is negative of E aa
B is always less than E aa
C can be less than or more than E aa
D is always double of E aa
Correct Answer
Option C
Solution

The energy of activation of reverse reaction is less than or more than energy of activation E

aa

of forward reaction

ΔH=(Ea)F(Ea)R\Delta H = {\left( {{E_a}} \right)_F} - {\left( {{E_a}} \right)_R}

Because it depends upon the nature of reaction. If

(Ea)F>(Ea)R{\left( {{E_a}} \right)_F} > {\left( {{E_a}} \right)_R}

, reaction is endothermic. or

(Ea)F<(Ea)R{\left( {{E_a}} \right)_F} < {\left( {{E_a}} \right)_R}

, reaction is exothermic.

Q56
2A \to B + C It would be a zero order reaction when
A the rate of reaction is proportional to square of concentration of A
B The rate of reaction remains same at any concentration of A
C the rate remains unchanged at any concentration of B and C
D the rate of reaction doubles if concentrations of B is increased to double.
Correct Answer
Option B
Solution

2A \to B + C If it is zero order reaction r = k [A] o . i.e the rate remains same at any concentration of 'A'. i.e independent upon concentration of A.

Q57
When a bio-chemical reaction is carried out in laboratory, outside the human body in absence of enzyme, then rate of reaction obtained is 10 -6 times, the activation energy of reaction in the presence of enzyme is
A 6/RT
B P is required
C different from E aa obtained in laboratory
D can't say anything.
Correct Answer
Option C
Solution

From Arrhenius equation, k = Ae –E a /RT The activation energy of the reaction in the presence of enzyme is different from E a obtained in laboratory.

Q58
For the reaction; 2N 2 O 5 \to 4NO 2 + O 2 rate and rate constant are 1.02 × \times 10 -4 and 3.4 × \times 10 -5 sec -1 respectively, then concentration of N 2 O 5 at that time will be
A 1.732
B 3
C 1.02 × \times 10 -4
D 3.4 × \times 10 5
Correct Answer
Option B
Solution

For the reaction; 2N 2 O 5 \to 4NO 2 + O 2 This is a first order reaction. \therefore rate = k [N 2 O 5 ] ; [N 2 O 5 ] =

ratek{{rate} \over k}

=

1.02×1043.4×105{{1.02 \times {{10}^{ - 4}}} \over {3.4 \times {{10}^{ - 5}}}}

= 3

Q59
How enzymes increases the rate of reactions
A by lowering activation energy
B by increaing activation energy
C by changing equilibrium constant
D by forming enzyme substrate complex.
Correct Answer
Option A
Solution

Enzymes act like catalyst in biochemical reactions.

Presence of an enzyme increases the rate of reaction by lowering the activation energy of the reactant.

Q60
For the reaction H + + BrO3_3^ - + 3Br - \to 5Br 2 + H 2 O which of the following relation correctly represents the consumption and formation of products.
A d[Br]dt=35d[Br2]dt{{d\left[ {B{r^ - }} \right]} \over {dt}} = - {3 \over 5}{{d\left[ {B{r_2}} \right]} \over {dt}}
B d[Br]dt=35d[Br2]dt{{d\left[ {B{r^ - }} \right]} \over {dt}} = {3 \over 5}{{d\left[ {B{r_2}} \right]} \over {dt}}
C d[Br]dt=53d[Br2]dt{{d\left[ {B{r^ - }} \right]} \over {dt}} = - {5 \over 3}{{d\left[ {B{r_2}} \right]} \over {dt}}
D d[Br]dt=53d[Br2]dt{{d\left[ {B{r^ - }} \right]} \over {dt}} = {5 \over 3}{{d\left[ {B{r_2}} \right]} \over {dt}}
Correct Answer
Option A
Solution
13- {1 \over 3}
d[Br]dt=+15d[Br2]dt{{d\left[ {B{r^ - }} \right]} \over {dt}} = + {1 \over 5}{{d\left[ {B{r_2}} \right]} \over {dt}}

\Rightarrow

d[Br]dt=35d[Br2]dt{{d\left[ {B{r^ - }} \right]} \over {dt}} = - {3 \over 5}{{d\left[ {B{r_2}} \right]} \over {dt}}
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