The study of the isomerization of trans-3-acetoxy-2-bromocyclooctene

<p>The isomerization of trans-3-acetoxy-2-bromocyclooctene (trans-1) to cis-3-acetoxy-2-bromocyclooctene (cis-1) was studied, trans-3- Methoxy-2-bromocyclooctene (trans-2) was used as a model compound for comparison. The rate of isomerization of both compounds increased tremendously with iodine (free radical catalysis) and decresed tremendously in the presence of hydroquinone (free radical inhibitor). This showed that the isomerizations of trans-1 and trans-2 are free radical catalyzed. It was anticipated that acetoxyl participation in trans-1, by stabilizing the free radical intermediate, would cause the rate of rearrangement of trans-1 to be much greater than the rate of rearrangement of trans-2. However, trans-1 iscented only about four times faster then trans-2. These results neither clearly establish nor rule out acetoxyl participation in the rear- rangement of trans-1</p>

Name thesis:degree_name

Master of Science (M.S.)

Level thesis:degree_level

Thesis

Discipline thesis:degree_discipline

Graduate School

Year dc:date.available

1972

Author dc:creator

• Lewis, Virginia Hill

Contributors dc:contributor

• Emensdy

• Isomerization
• Radicals (Chemistry)
• trans 1
• trans2
• Iodine
• Chemistry

Licence

• http://rightsstatements.org/vocab/NKC/1.0/

Repository record dc:identifier

https://scholarlycommons.pacific.edu/uop_etds/1767

OAI identifier oai:identifier

oai:scholarlycommons.pacific.edu:uop_etds-2766