Effect of structure on reactivity in oxi
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M. Calzadilla; A. Malpica; T. Cordova
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Article
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1999
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John Wiley and Sons
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English
โ 58 KB
๐ 2 views
Second-order rate constants for substituted benzaldehyde oxime formation increase linearly with the activity of hydrated protons over the pH range ca 2-7. Under these conditions, first-order rate constants show saturation behavior with increasing hydroxylamine concentration, establishing carbinolami