Home > Iowa Academy of Science > Journals & Newsletters > Proceedings of the Iowa Academy of Science > Volume 34 (1927) > Annual Issue
Document Type
Research
Abstract
It is known that phenyl alkyl ethers substitute in the phenyl radical less easily than phenol; nevertheless, phenetol will give a tribromophenyl compound. When the allyl derivative is used, both phenyl and allyl radicals may be involved in the change. Experiments now in progress show that rearrangement of the allyl ether by heat, according to Claisen's method may cause a loss of bromine.
Publication Date
1927
Journal Title
Proceedings of the Iowa Academy of Science
Volume
34
Issue
1
First Page
222
Last Page
223
Copyright
©1927 Iowa Academy of Science, Inc.
Language
en
File Format
application/pdf
Recommended Citation
Raiford, L. Chas. and Birosel, D. M.
(1927)
"Steric Hindrance in the Behavior of Phenyl Alkyl Ether and Derivatives,"
Proceedings of the Iowa Academy of Science, 34(1), 222-223.
Available at:
https://scholarworks.uni.edu/pias/vol34/iss1/53