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<records>
<record>
<language>eng</language>
<publisher>Science and Education Publishing</publisher>
<journalTitle>World Journal of Chemical Education</journalTitle>
<eissn>2375-1657</eissn>
<publicationDate>2025-09-24</publicationDate>
<volume>13</volume>
<issue>3</issue>
<startPage>65</startPage>
<endPage>90</endPage>
<doi>10.12691/wjce-13-3-5</doi>
<publisherRecordId>WJCE20251335</publisherRecordId>
<documentType>article</documentType>
<title language="eng">A Deep Insight into the Application of Linear Free Energy Relationships (LFER) to Five Membered Heterocyclic Ring Systems: A Chemical Education Review for Graduate Students</title>
<authors>
<author>
<name>Sanjeev Rachuru</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>V. Jagannadham</name>
<email>jagannadham1950@yahoo.com</email>
<affiliationId>2</affiliationId>
</author>

</authors>
<affiliationsList>
<affiliationName affiliationId="1">Department of Chemistry, St. Ann's College for Women, Mehdipatnam Hyderabad-500028, India</affiliationName>
<affiliationName affiliationId="2">Department of Chemistry, Osmania University, Hyderabad-500007, India</affiliationName>
</affiliationsList>
<abstract language="eng">Hammett and Taft equations are applied to the acid dissociation equilibriums of 4 and 5-substituted furan, pyrrole, thiophene, tellurophene, isoxazole, pyrazole carboxylic acids, to solvolysis data of 4 and 5-substituted-2-furylmethylcarbinyl p-nitrobenzoates and to the permanganate ion oxidation of 5-substituted-2-furfurals. Excellent correlations were observed in these studies except in the case of 1-Me-4/5-X-3-pyrazole-COOH. In the case of 5-X-2-furoic, pyrrole, thiophene carboxylic acids only the substituent -COOH deviated from these correlations for which possible explanation is given in terms of intramolecular hydrogen bonding between the -COOH and the ring heteroatom and two types of intramolecular hydrogen bonding between -COOH and ring nitrogen atom and -COOH and H of NH of pyrrole. In the case of 3,5-X-4-isoxazole carboxylic acids the -NH2 group at 5 position deviated for which the explanation in terms of H-bonding between -NH2 and -COOH is given. Even the possibility of the formation of zwitterion is not ruled out. 5-X-1,2,3-triazole-4-carboxylic acids did not follow any LFER. The solvolysis rate constants of both 4 and 5-substituted-2-furylmethylcarbinyl p-nitrobenzoates correlated well with para substituent constants. Further the correlation with BrownĄŻs + values is still better. It is noteworthy that MnO4- oxidation of 5-X-2-furfural correlated well with all the para, meta and ortho substituent constants. An attempt is made for the first time by our laboratory to apply the LFER to 5 membered ring systems with one heteroatom viz. pyrroles, two heteroatoms viz. pyrazoles, imidazoles, isoxazoles, three heteroatoms viz. the triazoles and four heteroatoms viz. tetrazoles. For the first time we have shown that the pKa values of N(1)H-acidities of 3-X-pyrroles, 3-X-pyrazoles, 4-X-pyrazoles, 4-X-imidazoles, 3-X-1,2,4-triazole, 4-X-1,2,3-triazole and 5-X-1,2,3,4-tetrazoles correlated well with Hammett  values.</abstract>
<fullTextUrl format="pdf">https://pubs.sciepub.com/wjce/13/3/5/wjce-13-3-5.pdf</fullTextUrl>
<keywords language="eng"><keyword>Hammett equation</keyword>
<keyword>Taft equation</keyword>
<keyword>5-membered heterocycles</keyword>
</keywords>
</record>
</records>
