To solve the problem, we need to determine how the rate of a second-order reaction is affected when the concentration of the reactant is (i) doubled and (ii) reduced to half.
1. Understand the Rate Law:
For a second-order reaction with respect to a reactant A, the rate law is \( \text{Rate} = k [A]^2 \), where \( k \) is the rate constant and \( [A] \) is the concentration of the reactant.
2. Case (i) - Concentration Doubled:
If the concentration is doubled, \( [A] \) becomes \( 2[A] \). The new rate is:
\( \text{Rate}_{\text{new}} = k (2[A])^2 = k \cdot 4[A]^2 = 4 \times \text{Rate}_{\text{initial}} \).
The rate increases by a factor of 4.
3. Case (ii) - Concentration Reduced to Half:
If the concentration is reduced to half, \( [A] \) becomes \( \frac{1}{2}[A] \). The new rate is:
\( \text{Rate}_{\text{new}} = k \left(\frac{1}{2}[A]\right)^2 = k \cdot \frac{1}{4}[A]^2 = \frac{1}{4} \times \text{Rate}_{\text{initial}} \).
The rate decreases to one-fourth of the initial rate.
Final Answer:
(i) The rate increases by a factor of 4 when the concentration is doubled.
(ii) The rate decreases to one-fourth when the concentration is reduced to half.
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.