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Thermodynamic data for the effect of substituents on the strength of Hetero-Intermolecular Hydrogen Bonds. l’art II.

Year 1981, Volume: 27 , 0 - 0, 01.01.1981
https://doi.org/10.1501/Commub_0000000131
https://izlik.org/JA66AC89HK

Abstract

Hetero-association constants and enthalpy changes are estimated for the hetero-association reactions between trifluoroacetic acid and each of p-nitro and p-meythylbenzophenones, at the temperature range 35-55 . The results show that the presence of the p-nitro group in the benzop- henone molecule weakens the hydrogen bonds formed between trifluoroacetic acid and benzop- henone, whereas the p-methyl group strengthens such bonds.

References

  • Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering

Year 1981, Volume: 27 , 0 - 0, 01.01.1981
https://doi.org/10.1501/Commub_0000000131
https://izlik.org/JA66AC89HK

Abstract

References

  • Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
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Details

Primary Language English
Subjects Chemical Engineering
Journal Section Research Article
Authors

A. A. Taha This is me

Publication Date January 1, 1981
DOI https://doi.org/10.1501/Commub_0000000131
IZ https://izlik.org/JA66AC89HK
Published in Issue Year 1981 Volume: 27

Cite

Vancouver 1.Taha AA. Thermodynamic data for the effect of substituents on the strength of Hetero-Intermolecular Hydrogen Bonds. l’art II. Commun. Fac. Sci. Univ. Ank. Ser. B [Internet]. 1981 Jan. 1;27. Available from: https://izlik.org/JA66AC89HK

Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering

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