๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Solvolysis of trans-cyclooct-2-enyl 3,5-dinitrobenzoates

โœ Scribed by Kenneth B. Wiberg; Takayuki Nakahira


Book ID
104234905
Publisher
Elsevier Science
Year
1974
Tongue
French
Weight
143 KB
Volume
15
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Relative solvolysis rates of allyl and d
โœ Nye A. Clinton; C.Peter Lillya ๐Ÿ“‚ Article ๐Ÿ“… 1968 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 178 KB

Of the many solvolysis rate studies involving ally1 compounds, only two have examined the effect of extending conjugation. Vernon' has estimated that replacement of a p-methyl group by a phenyl group (1. and 2) increases the rate by a factor of gg. 140. Friedrich and WinsteIn have studied some spiro

Solvolysis of spiro[2.n]alkyl-4 dinitrob
โœ Kenneth B. Wiberg; John E. Hiatt ๐Ÿ“‚ Article ๐Ÿ“… 1968 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 170 KB

H. C. Brown and G. Ham, J.Am. Chem,Soc, && 2735 (1956) found a cyclopentyl/ cyclohexyl rate ratio of 14. Cyclobutyl tosylate is 11 timae as reactive as cyclohexyl tosylate.' Correcting for the 7OO:l ratio found with I and III, one obtains a rate acceleration of 8X10' for cyclobutyl tosylate.