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Additional Data on the cis and trans Isomers of Pentene-2

✍ Scribed by Sherrill, Mary L.; Matlack, Elizabeth S.


Book ID
127282425
Publisher
American Chemical Society
Year
1937
Tongue
English
Weight
547 KB
Volume
59
Category
Article
ISSN
0002-7863

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πŸ“œ SIMILAR VOLUMES


cis and trans Isomers of 2-Styrylpyridin
✍ WILLIAMS, J. L. R.; WEBSTER, S. K.; ALLAN, J. A. Van πŸ“‚ Article πŸ“… 1961 πŸ› American Chemical Society 🌐 English βš– 366 KB
H2S-promoted thermal isomerization of ci
✍ D. Perrin; C. Richard; R. Martin πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 457 KB

H,S accelerates the thermal isomerization of cis-2-pentene (P2c) to 1-pentene (P1) and trans-2-pentene (P2t) to around 800 K. This effect is interpreted on the basis of a free radical mechanism in which 2-pentenyl and thiyl radicals are the main chain carriers. P1 formation is essentially explained

Polymerization ability of cis- and trans
✍ Yokoyama, Y. ;Hall, H. K. πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons βš– 491 KB

## Abstract The behavior of the readily available __cis__‐ (**1**) and __trans__‐ (**2**) 4, 5‐epoxy‐2‐pentenals toward classical cationic, anionic, and free radical initiators has been examined. Only the cationic polymerization of **1** gave soluble polymer of moderate molecular weights. This poly