From Mock A · Paper 2: Organic and Physical Chemistry
4.16 marks
Compound X, C₄H₈O₂, has an IR absorption at 1740 cm⁻¹ and no broad absorption at 2500–3300 cm⁻¹. Its ¹H NMR spectrum shows:
Deduce the structure of X, explaining your reasoning.
| δ / ppm | Integration | Splitting |
|---|---|---|
| 4.1 | 2 | quartet |
| 2.0 | 3 | singlet |
| 1.2 | 3 | triplet |