<?xml version="1.0" encoding="UTF-8"?>
<records>
<record>
<language>eng</language>
<publisher>Science and Education Publishing</publisher>
<journalTitle>World Journal of Chemical Education</journalTitle>
<eissn>2375-1657</eissn>
<publicationDate>2021-11-15</publicationDate>
<volume>9</volume>
<issue>3</issue>
<startPage>94</startPage>
<endPage>95</endPage>
<doi>10.12691/wjce-9-3-5</doi>
<publisherRecordId>WJCE2021935</publisherRecordId>
<documentType>article</documentType>
<title language="eng">Why the Second Bond Exceptionally Effective on pKa Values of -ynoic (-C¡ÔC-) Compounds? Chemical Education Perspective</title>
<authors>
<author>
<name>R. Sanjeev</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>D. A. Padmavati</name>
<affiliationId>2</affiliationId>
</author>
<author>
<name>V. Jagannadham</name>
<email>jagannadham1950@yahoo.com</email>
<affiliationId>2</affiliationId>
</author>

</authors>
<affiliationsList>
<affiliationName affiliationId="1">Department of Chemistry, Geethanjali College of Engineering and Technology, Cheeryal-501301, Telangana, India</affiliationName>
<affiliationName affiliationId="2">Department of Chemistry, Osmania University, Hyderabad-500007, India</affiliationName>

</affiliationsList>
<abstract language="eng">Sudden decrease of nearly more than two orders of magnitude of pKa units of ynoic series of compounds is explained based on the electronegativity differences of sp, sp2 and sp3 carbons and on the subsequent stability of the corresponding anions. Both resonance and inductive effects operate in tandem to stabilize the ynoic anions.</abstract>
<fullTextUrl format="pdf">http://pubs.sciepub.com/wjce/9/3/5/wjce-9-3-5.pdf</fullTextUrl>
<keywords language="eng"><keyword>Ynoic compounds</keyword>
<keyword>chemical education</keyword>
<keyword>graduate research; pH and pK<SUB>a</SUB></keyword>
</keywords>
</record>
</records>
