Answer:
(a) Non-spontaneous. \(\Delta H = 50\) kJ, \(\Delta S = -130\) J K–1 \(= -0.130\) kJ K–1, \(T = 250\) K.
\(\Delta G = \Delta H - T\Delta S = 50 - 250(-0.130) = 50 + 32.5 = +82.5\) kJ
Since \(\Delta G \gt 0\), the reaction is non-spontaneous. (With \(\Delta H\) positive and \(\Delta S\) negative, \(\Delta G\) is positive at every temperature.)
(b) Optical activity of 2-chlorobutane: In CH3–CH2–C*H(Cl)–CH3, carbon-2 is attached to four different groups (–H, –Cl, –CH3 and –C2H5), so it is a chiral (asymmetric) carbon. The molecule therefore has no plane of symmetry and is not superimposable on its mirror image. It exists as two enantiomers: one rotates plane-polarised light to the right, (+) or dextrorotatory, and the other to the left by the same angle, (–) or laevorotatory. An equimolar mixture of the two is a racemic mixture and is optically inactive.
(c) DDT: p,p′-Dichlorodiphenyltrichloroethane [IUPAC: 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane].