Abstract
dc:descriptionCarbocations are typically formed in solution, where the solvent stabilizes thecarbocation and mixes the reaction allowing the particles to interact and form products. However, in the absence of solvent it is unknown if the carbocation will form. Previous literature has shown that S<sub>N</sub>2 reactions can occur under high speed ball milling conditions; the results were that primary alkyl halides undergo substitution reactions, while the reactions of secondary alkyl halides depend on the nucleophile. However, reactions that form a carbocation intermediate, such as, S<sub>N</sub>1 reaction and pinacol rearrangement have not been explored, until now.
Degree
thesis:*- Name thesis:degree_name
- MS
- Level thesis:degree_level
- masters
- Discipline thesis:degree_discipline
- Arts and Sciences: Chemistry
- Grantor dc:publisher
- University of Cincinnati
- Year dc:date
- 2012
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Wagner, Meghan
- Contributors dc:contributor
-
- Mack, James
Subjects
dc:subject × 1Rights
dc:rights- Statement dc:rights
-
- unrestricted
- This thesis or dissertation is protected by copyright: all rights reserved. It may not be copied or redistributed beyond the terms of applicable copyright laws.
- Language dc:language
- English
Identifiers
dc:identifier.*- Repository record dc:identifier
- http://rave.ohiolink.edu/etdc/view?acc_num=ucin1352402944
- OAI identifier oai:identifier
- oai:etd.ohiolink.edu:ucin1352402944