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Western Kentucky University
Conformational Analysis of 1-Tertiarybutyl-1, 4-Dihydronaphthalene a Turnover from SRNI to SNI Mechanism
Abstract
dc:description.abstract<p>The cyclohexadiene porition of 1-tertiarybutyl-1, 4-dihydronaphthalene exists in a puckered rather than planar conformation at room temperature, with approximately equal populations of the isomer with the t-butyl group “axial” and “equatorial.” Analysis of chemical shifts and coupling constants was aided by use of a LAOCOON III program. </p>
Degree
thesis:*- Name thesis:degree_name
- Master of Science
- Discipline thesis:degree_discipline
- Department of Chemistry
- Year
- 1977
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Huang, Su-Jen
- Contributors dc:contributor
-
- Norman Holy
Subjects
dc:subject × 1Identifiers
dc:identifier.*- Repository record dc:identifier
- https://digitalcommons.wku.edu/theses/1425
- OAI identifier oai:identifier
- oai:digitalcommons.wku.edu:theses-2432