Q1 · Dec 2019 · 2 marks
The oxidation of NO to \mathrm{NO_2} occurs via the mechanism given below. \mathrm{2NO \underset{k_{-1}}{\overset{k_1}{\rightleftharpoons}} N_2O_2}; \mathrm{N_2O_2 + O_2 \xrightarrow{k_2} 2NO_2}
\frac{d[\mathrm{NO_2}]}{dt} in the presence of large excess of \mathrm{O_2} can be written as - (a) 2k_1(\mathrm{NO})^2
- (b) 2k_1k_2(\mathrm{NO})^2(\mathrm{O_2})
- (c) \frac{k_1}{k_2}(\mathrm{NO})^2
- (d) 2k_2(\mathrm{NO})^2
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Answer: (a)
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Q2 · Dec 2019 · 2 marks
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Answer: (a)
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Q3 · June 2016 · 2 marks
Experimentally determined rate law for the chemical reaction, \mathrm{2NO_2F \rightarrow 2NO_2 + F_2} is R = k[\mathrm{NO_2F}] The rate determining step consistent with the rate law is
- (a) \mathrm{2NO_2F \rightarrow 2NO_2 + F_2}
- (b) \mathrm{NO_2F + F \rightarrow NO_2 + F_2}
- (c) \mathrm{NO_2F \rightarrow NO_2 + F}
- (d) \mathrm{NO_2 + F \rightarrow NO_2F}
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Answer: (c)
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Q4 · Dec 2016 · 2 marks
According to the transition state theory, the plot with slope equal to \frac{\Delta H^{\ddagger}}{R} is
- (a) \ln k vs. T
- (b) \ln\frac{k}{T} vs T
- (c) \ln\frac{k}{T} vs \frac{1}{T}
- (d) \ln k vs. \frac{1}{T}
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Answer: (c)
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Q5 · June 2015 · 2 marks
In a photochemical reaction, radicals formed according to the equation \begin{array}{l} \mathrm{C}_{4} \mathrm{H}_{10}+\mathrm{hv} \sqrt{ } 2 \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{C}_{2} \mathrm{H}_{5}+\mathrm{C}_{2} \mathrm{H}_{5} \xrightarrow{k_{2}} \mathrm{C}_{2} \mathrm{H}_{6}+\mathrm{C}_{2} \mathrm{H}_{4} \end{array}
If I is the intensity of light absorbed, the rate of the overall reaction is proportional to- - (a) I
- (b) \mathrm{I}^{1 / 2}
- (c) \mathrm{I}\left[\mathrm{C}_{4} \mathrm{H}_{10}\right]
- (d) \mathrm{I}^{1 / 2}\left[\mathrm{C}_{4} \mathrm{H}_{10}\right]^{1 / 2}
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Answer: (d)
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Q6 · Dec 2014 · 2 marks
For an enzyme-substrate reaction, a plot between \frac{1}{v} and \frac{1}{[S O]} yields a slope of 40 s . If the enzyme concentration is \mathbf{2 . 5} \mu \mathbf{M}, then the catalytic efficiency of the enzyme is (1) 40 \mathrm{Lmol}^{-\mathbf{1}} \mathrm{s}^{-\mathbf{1}} (2) \mathbf{1 0}^{-\mathbf{4}} \mathbf{~ L m o l}^{-\mathbf{1}} \mathbf{s}^{-\mathbf{1}} (3) \mathbf{1 0}^{\mathbf{7}} \mathbf{~ L m o l}^{\boldsymbol{-} \mathbf{1}} \mathbf{s}^{\mathbf{- 1}} (4) \mathbf{1 0}^{\mathbf{4}} \mathbf{~ L m o l}^{\boldsymbol{-} \mathbf{1}} \mathbf{s}^{\boldsymbol{-} \mathbf{1}} 38. For a gaseous reaction, \mathbf{2 N O}(\mathbf{g})+\mathbf{C l}_{\mathbf{2}}(\mathbf{g})-\mathbf{N o n}-linear T.S.-2NOCl, the pre-exponential factor in the rate constant is proportional to
- (a) \mathbf{T}^{\mathbf{1} / \mathbf{2}}
- (b) \mathrm{T}^{-1 / 2}
- (c) \mathrm{T}^{-5 / 2}
- (d) \mathrm{T}^{-7 / 2}
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Answer: (d)
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Q7 · Dec 2014 · 2 marks
The rate constant for a reaction A^{1+}+B^{n+1} \rightarrow P is measured in two different aqueous solutions of ionic strengths \mathbf{0 . 0 1 ~ M} and \mathbf{0 . 0 4 ~ M}. If \boldsymbol{\operatorname { l o g }}_{\mathbf{K 0 . 0 1}} \frac{K 0.04}{\mathbf{K}}=\mathbf{0 . 3}, the charge n on B is closest to
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Answer: (c)
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Q8 · Dec 2013 · 2 marks
A first order gaseous reaction is 25 \% complete in 30 minutes at 227^{\circ} \mathrm{C} and in 10 minutes at 237^{\circ} \mathrm{C}. The activation energy of the reaction is closest to \left(\mathrm{R}=2 \mathrm{cal} \mathrm{K}^{-1} \mathrm{~mol}^{-1}\right)
- (a) 27 \mathrm{kcal} \mathrm{mol}^{-\mathbf{1}}
- (b) \mathbf{1 1 0 ~ k c a l ~ m o l}^{\boldsymbol{-} \mathbf{1}} (3) 55 \mathrm{kcal} \mathrm{mol}^{-\mathbf{1}} (4) 5.5 \mathrm{kcal} \mathrm{mol}^{-1}
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Answer: (c)
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Q9 · Dec 2013 · 2 marks
For a first order reaction \mathrm{A} \rightarrow products, the plot of \mathrm{In}\left(\frac{[A]_{t}}{[A]_{0}}\right) v s time, where [\mathrm{A}]_{0} and [\mathrm{A}]_{t} to cocentration at time =0 and t respectively, is
- (a) a straight line with a positive slope passing through origin
- (b) a straight line with a negative slope passing through origin.
- (c) an exponential curve asymptotic to the time axis
- (d) a curve asymptotic to the \operatorname{In}\left(\frac{[A]_{t}}{[A]_{0}}\right) axis.
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Answer: (b)
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Q10 · Dec 2012 · 2 marks
The decomposition of \mathrm{NH}_3 on Mo surface follows Langmuir-Hinshelwood mechanism. The decomposition was carried out at low pressures. The initial pressure of \mathrm{NH}_3 was 10^{-2} torr. The pressure of \mathrm{NH}_3 was reduced to 10^{-4} torr in 10 minutes. The rate constant of decomposition of \mathrm{NH}_3 is:
- (a) 9.9 \times 10^{-4}\ \mathrm{torr\ min^{-1}}
- (b) 0.4606\ \mathrm{min^{-1}}
- (c) 9.9 \times 10^{-3}\ \mathrm{torr\ min^{-1}}
- (d) 0.693\ \mathrm{min^{-1}}
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Answer: (b)
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Q11 · Dec 2012 · 2 marks
The rate equation for the reaction 2 \mathrm{AB}+\mathrm{B}_{2} \rightarrow 2 \mathrm{~A} \mathrm{~B}_{2} is given by \text { rate }=k[A B]\left[B_{2}\right]
A possible mechanism consistent with this rate law is - (a) \mathbf{2 A B}+\mathbf{B}_{\mathbf{2}} \xrightarrow{\text { slow }} \mathbf{2} \mathbf{A B}_{\mathbf{2}}
- (b) \mathbf{A B}+\mathbf{A B} \leftrightharpoons \mathbf{A}_{\mathbf{2}} \mathbf{B}_{\mathbf{2}} (fast)
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Answer: (c)
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Q12 · Dec 2011 · 2 marks
One of the assumptions made in the conventional activated complex theory is:
- (a) Equilibrium is maintained between reactants and the activated complex
- (b) Equilibrium is maintained between the reactants and the products.
- (c) Equilibrium is maintained between the products and the activated complex
- (d) Equilibrium is maintained between the reactants, the activated complex and the products.
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Answer: (a)
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Q13 · Dec 2011 · 2 marks
An example of a relaxation method of measuring rates is:
- (a) Spectroscopic monitoring of product concentration.
- (b) Stopped flow technique
- (c) Temperature jump experiments.
- (d) Measurement of spectral line widths.
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Answer: (c)
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Q14 · Dec 2011 · 2 marks
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Answer: (d)
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Q15 · Dec 2011 · 2 marks
"Phosphorescence" is represented as
- (a) T_1 \rightarrow S_0 + h\nu
- (b) T_1 \rightarrow S_0 + \Delta
- (c) S_1 \rightarrow S_0 + h\nu
- (d) S_1 \rightarrow T_1 + \Delta
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Answer: (a)
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Q16 · Dec 2011 · 2 marks
Using cuvettes of 0.5 cm path length, a 10^{-4} M solution of a chromophore shows 50% transmittance at certain wave length. The molar extinction coefficient of the chromophore at this wave length is (\log 2 = 0.301)
- (a) 1500\ \mathrm{M^{-1}\,cm^{-1}}
- (b) 3010\ \mathrm{M^{-1}\,cm^{-1}}
- (c) 5000\ \mathrm{M^{-1}\,cm^{-1}}
- (d) 6020\ \mathrm{M^{-1}\,cm^{-1}}
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Answer: (d)
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