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Strong covalent hydration of terephthalaldehyde
Authors:Baymak Melek S  Vercoe Kellie L  Zuman Petr
Institution:Department of Chemistry, Clarkson University, Potsdam, New York 13699-5810, USA.
Abstract:Spectrophotometric and electroanalytical studies indicate that one of the formyl groups of terephthalaldehyde in aqueous solution is present in about 23% as a geminal diol. Stronger covalent hydration of CHO in terephthalaldehyde than in p-nitrobenzaldehyde is attributed to a strong resonance interaction between the two formyl groups.
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