5. A compound has the molecular formula, C₆H₁₂O₂. Its IR spectrum shows a strong absorption band near 1740 cm⁻¹; its ¹H NMR spectrum consists of two singlets, at δ 1.2 and 3.6 ppm. The most likely structure for this compound is: (A) Isopropyl propionate (B) Propyl propionate (C) Ethyl isobutyrate (D) tert-Butyl acetate (E) Methyl pivalate

11. At some temperatures, the relative reactivities of 3°, 2° and 1° alkane hydrogens in free radical chlorination are in the ratio of 5:3:1. What would be the expected percentages of monochlorination of isopentane produced? (i) 2-chloro-2-methylbutane, (ii) combined 1-chloro-2-methylbutane and 1-chloro-3-methylbutane, and (iii) 2-chloro-3-methylbutane. (A) 10% (i), 75% (ii), 15% (iii) (B) 25% (i), 45% (ii), 30% (iii) (C) 29% (i), 44% (ii), 18% (iii) (D) 30% (i), 35% (ii), 35% (iii) (E) 36% (i), 43% (ii), 21% (iii)

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