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Inductive and hyperconjugative effects in the solvolysis of 4-substituted bicyclo[2.2.2]Oct-1-yl p-nitrobenzenesulfonates

✍ Scribed by C.A. Grob; R. Rich


Publisher
Elsevier Science
Year
1978
Tongue
French
Weight
164 KB
Volume
19
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES


Polar Effects in the Solvolysis of 4-Sub
✍ Cyril A. Grob; Roland Rich πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 German βš– 415 KB πŸ‘ 1 views

Hydrolysisofbicyclo[2.2.2]octylp-nitrobenzenesulfonate (14a,X =p-N02C6H4S03), and nineteen 4-R-substituted derivatives 14b-14 t in 70% aqueous dioxane yield the corresponding bicyclo [2.2.2]octanols 14 (X = OH), exclusively. The 7-center fragmentation to 1,4-dimethylidene-cyclohexane (15) is not obs

Polar effects. Part 12. Inductivity and
✍ Cyril A. Grob; Gerhard Wittwer; K. Rama Rao πŸ“‚ Article πŸ“… 1985 πŸ› John Wiley and Sons 🌐 German βš– 480 KB πŸ‘ 1 views

## Abstract The rate constants (log __k__) for the solvolysis of 4^e^‐substituted 2^e^‐ and 2^a^‐adamantyl __p__‐nitrobenzenesulfonates **14** and **15**, respectively, in 80% EtOH correlate linearly with the respective inductive substituent constants Οƒ. Therefore, relative rates are controlled by