To solve the problem, we need to identify which among the given statements about reaction kinetics is false.
1. Analyzing Statement (A):
Rate of a zero-order reaction is independent of the initial concentration of reactant. For a zero-order reaction, the rate law is $ \text{Rate} = k $, which does not depend on concentration. This statement is true.
2. Analyzing Statement (B):
Half-life of a zero-order reaction is inversely proportional to the rate constant. The half-life for a zero-order reaction is given by $ t_{1/2} = \frac{[A]_0}{2k} $, where $ [A]_0 $ is the initial concentration. The half-life depends on $ [A]_0 $ and $ k $, but the statement claims it’s inversely proportional to the rate constant $ k $. Since $ t_{1/2} \propto \frac{1}{k} $, this statement is true.
3. Analyzing Statement (C):
Molecularity of a reaction may be zero. Molecularity represents the number of molecules colliding in an elementary reaction step and must be a positive integer (1, 2, or 3). It cannot be zero, as that would imply no molecules are involved, which is not possible for a reaction. This statement is false.
4. Analyzing Statement (D):
For a first-order reaction, $ t_{1/2} = 0.693/k $. For a first-order reaction, the half-life is $ t_{1/2} = \frac{\ln(2)}{k} \approx \frac{0.693}{k} $, which matches the given formula. This statement is true.
Final Answer:
The false statement is (C) Molecularity of a reaction may be zero.
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 \(8 \ hours\)?