Amines have a lone pair of electrons on the nitrogen atom, due to which they behave as Lewis bases. Greater the value of \( K_b \) or smaller the value of \( pK_b \), stronger is the base. Amines are more basic than alcohols, ethers, esters, etc. The basic character of aliphatic amines should increase with the increase of alkyl substitution. However, it does not occur in a regular manner, as a secondary aliphatic amine is unexpectedly more basic than a tertiary amine in aqueous solutions. Aromatic amines are weaker bases than ammonia and aliphatic amines. Electron-releasing groups such as \( -CH_3 \), \( -NH_2 \), etc., increase the basicity, while electron-withdrawing substituents such as \( -NO_2 \), \( -CN \), halogens, etc., decrease the basicity of amines. The effect of these substituents is more pronounced at the para-position than at the meta-position.
(a) Arrange the following in increasing order of their basic character. Give reason:
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Assertion (A): All naturally occurring \(\alpha\)-amino acids except glycine are optically active. Reason (R): Most naturally occurring amino acids have L-configuration.
Assertion (A): The boiling point of ethanol is higher than that of methoxymethane. Reason (R): There is intramolecular hydrogen bonding in ethanol.
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): [Cr(H_2O)_6]Cl_2 and [Fe(H_2O)_6]Cl_2 are examples of homoleptic complexes. Reason (R): All the ligands attached to the metal are the same.
Which of the following statements is not true about glucose?