For a reaction:
\( 2 \text{H}_2\text{O}_2 \xrightarrow{\text{I}} 2 \text{H}_2\text{O} + \text{O}_2 \)
The proposed mechanism is as given below:
(I) \( \text{H}_2\text{O}_2 \xrightarrow{\text{slow}} \text{H}_2\text{O} + \text{IO}^- \) (slow)
(II) \( \text{H}_2\text{O}_2 + \text{IO}^- \xrightarrow{\text{fast}} \text{H}_2\text{O} + \text{I}^+ + \text{O}_2 \) (fast)
(I) The rate-determining step is the first reaction, where hydrogen peroxide decomposes to form water and IO−. The rate law for the reaction will be dependent on the concentration of H2O2.
(II) In the second step, the intermediate IO− reacts with H2O2 in a fast step to produce water, iodine ions, and oxygen gas. This step does not affect the rate law, as it is not rate-determining.
(1) Rate law: The rate law is determined by the slow step, so the rate law is:
Rate = \( k[\text{H}_2\text{O}_2] \)
where \( k \) is the rate constant.
(2) Overall order and molecularity: The overall order of the reaction is 1, as the rate law depends on the concentration of only one reactant, H2O2. The molecularity of the reaction is 2, as the rate-determining step involves the collision of two molecules of H2O2.
Write IUPAC names of the following compounds and classify them into primary, secondary and tertiary amines.
(i) (CH3 )2CHNH2 (ii) CH3 (CH2 )2NH2 (iii) CH3NHCH(CH3 )2
(iv) (CH3 )3CNH2 (v) C6H5NHCH3 (vi) (CH3CH2 )2NCH3 (vii) m–BrC6H4NH2
Give one chemical test to distinguish between the following pairs of compounds.
(i) Methylamine and dimethylamine
(ii) Secondary and tertiary amines
(iii) Ethylamine and aniline
(iv) Aniline and benzylamine
(v) Aniline and N-methylaniline
Account for the following:
(i) pKb of aniline is more than that of methylamine.
(ii) Ethylamine is soluble in water whereas aniline is not.
(iii) Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
(iv) Although amino group is o– and p– directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.
(v) Aniline does not undergo Friedel-Crafts reaction.
(vi) Diazonium salts of aromatic amines are more stable than those of aliphatic amines. (vii) Gabriel phthalimide synthesis is preferred for synthesising primary amines.
| Experiment | Time/s-1 | Total pressure/atm |
| 1 | 0 | 0.5 |
| 2 | 100 | 0.6 |
The rate constant for the decomposition of \(N_2O_5\) at various temperatures is given below:
| T/°C | 0 | 20 | 40 | 60 | 80 |
| 105 x k/s-1 | 0.0787 | 1.70 | 25.7 | 178 | 2140 |
Draw a graph between ln k and \(\frac 1T\) and calculate the values of \(A\) and \(E_a\).
Predict the rate constant at 30 ºC and 50 ºC.
The rate constant for the decomposition of hydrocarbons is 2.418 x 10-5 s-1 at 546 K. If the energy of activation is 179.9 kJ/mol, what will be the value of pre-exponential factor.
Consider a certain reaction \(A\) \(→\) \(Products\) with \(k = 2.0 \times 10^{-2 }s^{-1}\) . Calculate the concentration of A remaining after 100 s if the initial concentration of A is 1.0 mol L-1.
Sucrose decomposes in acid solution into glucose and fructose according to the first order rate law, with \(t_{\frac 12} = 3.00\ hours\). What fraction of sample of sucrose remains after \(8 \ hours\)?