(i) Enantiomers: Enantiomers are pairs of molecules that are non-superimposable mirror images of each other. They have identical physical properties but differ in their interaction with plane-polarized light and in the way they interact with other chiral substances. For example, the right- and left-handed forms of a chiral molecule are enantiomers.
(ii) Racemic mixture: A racemic mixture is a mixture containing equal amounts of two enantiomers of a chiral compound. In a racemic mixture, the optical activities of the enantiomers cancel each other out, resulting in no net optical rotation.
Assertion (A): All naturally occurring \(\alpha\)-amino acids except glycine are optically active. Reason (R): Most naturally occurring amino acids have L-configuration.
(a) State the following:
(i) Kohlrausch law of independent migration of ions
A solution of glucose (molar mass = 180 g mol\(^{-1}\)) in water has a boiling point of 100.20°C. Calculate the freezing point of the same solution. Molal constants for water \(K_f\) and \(K_b\) are 1.86 K kg mol\(^{-1}\) and 0.512 K kg mol\(^{-1}\) respectively.
Write the reactions involved when D-glucose is treated with the following reagents: (a) HCN (b) Br\(_2\) water
Identify A and B in each of the following reaction sequence:
(a) \[ CH_3CH_2Cl \xrightarrow{NaCN} A \xrightarrow{H_2/Ni} B \]
(b) \[ C_6H_5NH_2 \xrightarrow{NaNO_2/HCl} A \xrightarrow{C_6H_5NH_2} B \]
Would you expect benzaldehyde to be more reactive or less reactive in nucleophilic addition reactions than propanal? Justify your answer.