Actually ethyl acetoacetate exhibit keto-enol tautomerism. The keto form has two carbonyl groups with separate stretching frequencies at 1733 and 1710 cm-1 in FT-IR spectra. But in enol form only one carbonyl group present and exhibit frequency at 1645 cm-1 (because intramolecular hydrogen bonding lowers the carbonyl frequency) and also C=C stretching exhibit at 1650 cm-1 in enol form because of cyclization.