Assertion (A): The boiling points of alkyl halides decrease in the order: RI>RBr>RCl>RF.
Reason (R): The boiling points of alkyl chlorides, bromides and iodides are considerably higher than that of the hydrocarbon of comparable molecular mass.
Assertion (A) is false, but Reason (R) is true.
Step 1: Understanding the boiling point order. The boiling points of alkyl halides decrease in the order: \( \text{RI} > \text{RBr} > \text{RCl} > \text{RF} \) because the iodine atom is the largest halogen, leading to stronger dispersion forces and, consequently, higher boiling points.
Step 2: Reason for the boiling point order. While Reason (R) is true in stating that alkyl halides have higher boiling points compared to hydrocarbons of comparable molecular mass, it does not directly explain the order in which boiling points decrease. The reason for this specific order lies more in the halogen size and the resultant intermolecular forces.
Step 3: Conclusion. Thus, both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of Assertion (A). The correct answer is option (B).
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.
Give Reasons:
(I) \( \text{Ce}^{4+} \) in aqueous solution is a good oxidising agent.
(II) The actinoid contraction is greater from element to element than lanthanoid contraction.
(III) \( E^\circ_{\text{M}^{2+}/\text{M}} \) value is more negative than expected, whereas \( E^\circ_{\text{Cu}^{2+}/\text{Cu}} \) is positive.