Assertion (A): In a first order reaction, if the concentration of the reactant is doubled, its half-life is also doubled.
Reason (R): The half-life of a reaction does not depend upon the initial concentration of the reactant in a first order reaction.
To solve the problem, we need to evaluate the Assertion (A) and Reason (R) regarding the effect of doubling the reactant concentration on the half-life of a first order reaction and determine their validity and relationship.
1. Analyzing the Assertion (A):
Assertion (A) states that in a first order reaction, if the concentration of the reactant is doubled, its half-life is also doubled. For a first order reaction, the rate law is Rate = k[A], where k is the rate constant and [A] is the reactant concentration. The half-life (t\(_{1/2}\)) of a first order reaction is given by the formula:
$ t_{1/2} = \frac{\ln(2)}{k} \approx \frac{0.693}{k} $
This formula shows that the half-life depends only on the rate constant k and is independent of the initial concentration [A]\(_0\). If the initial concentration is doubled, the half-life remains the same because k does not change. Therefore, the assertion that doubling the concentration doubles the half-life is false, as the half-life stays constant.
2. Analyzing the Reason (R):
Reason (R) states that the half-life of a first order reaction does not depend upon the initial concentration of the reactant. As derived above, the half-life formula $ t_{1/2} = \frac{\ln(2)}{k} $ confirms that t\(_{1/2}\) is a function of k only and does not involve [A]\(_0\). This is a characteristic feature of first order reactions, unlike zero or second order reactions where half-life depends on concentration. Thus, the reason is true.
3. Evaluating the Relationship:
The assertion is false because doubling the reactant concentration does not affect the half-life in a first order reaction. The reason is true and directly contradicts the assertion, as it correctly states that the half-life is independent of initial concentration. In assertion-reason questions, if the assertion is false, the reason’s truth does not make the assertion true. However, the reason explains why the assertion is incorrect, as the independence of half-life from concentration means doubling the concentration cannot double the half-life.
4. Conclusion:
- Assertion (A) is false because the half-life of a first order reaction does not change when the reactant concentration is doubled.
- Reason (R) is true because the half-life of a first order reaction is independent of the initial concentration.
- The reason explains why the assertion is false, as the concentration independence of the half-life contradicts the claim that doubling concentration doubles the half-life.
Final Answer:
Assertion (A) is false, Reason (R) is true.
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 \(8 \ hours\)?