E-Journal of Chemistry (Jan 2009)

Studies of Hydrogen Bonding Between N, N-Dimethylacetamide and Primary Alcohols

  • M. S. Manjunath,
  • P. Sivagurunathan,
  • J. Sannappa

DOI
https://doi.org/10.1155/2009/120362
Journal volume & issue
Vol. 6, no. S1
pp. S143 – S146

Abstract

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Hydrogen bonding between N, N-dimethylacetamide (DMA) and alcohols has been studied in carbon tetrachloride solution by an X-band Microwave bench at 936GHz. The dielectric relaxation time (τ) of the binary system are obtained by both Higasi's method and Gopalakrishna method. The most likely association complex between alcohol and DMA is 1:1 stoichiometric complex through the hydroxyl group of the alcohol and the carbonyl group of amide. The results show that the interaction between alcohols and amides is 1:1 complex through the free hydroxyl group of the alcohol and the carbonyl group of amide and the alkyl chain-length of both the alcohols and amide plays an important role in the determination of the strength of hydrogen bond (O-H: C=O) formed and suggests that the proton donating ability of alcohols is in the order: 1-propanol < 1-butanol < 1-pentanol and the accepting ability of DMA.