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C4H5NO4 (C3H6NO2) Wikipedia is supplied by Jeff Titus at the University of New Hampshire, USA. to catalyze the reaction. The reaction is exothermic, with the formation of (C3H6O)x + H2SO4, where x 1.0.. on a single carbon atom. This is the highest value ever reported for any carbonate, or other complex. The unique properties of the C3H6O functional group arise from its ability to act as a H-bonding acceptor.. on complexation with metal(II) ions or metal(III) ions), C3H6O complexation of metal cations is known from NMR spectroscopy and X-ray crystallography.. aldehydes, and oxygen-containing aromatic compounds. The functional group is also stable. However, pyruvates (also referred to as (R)-pyruvic acid) and other pyruvates can be used as starting materials in… Analysis: Below the spectra of the C4H5NO4 are predicted with the aid of Gaussian09: The spectra of the full molecule (initial and predicted spectra together) are given below: In the first time, the bands at 1640 and 1725 cm(-1) have been decomposed into two bands at 1619 and 1697 cm(-1), respectively. The vibration of the carbonyl group, C=O is indeed split due to the existence of the double-bond stretching motion, without any change of stretching frequency. While in the predicted spectra of the C3H6O, the band at about 1619 cm(-1) is a shoulder with the other band at about 1697 cm(-1), the frequency of the C=O band is almost the same as that of the initial spectrum. The lower intensity of the band at 1697 cm(-1) indicates that the double-bond stretching motion is weakened. Moreover, a new band at 1740 cm(-1) is found in the predicted spectra, which corresponds to the C=O stretching vibration. The intensity of this band is larger than the rest, and the band is more intense than that of the band at about 1725 cm(-1). This may be attributed to the increased acidity of the carbonyl oxygen and the presence of an aldehyde group in the molecule, which make
