## Abstract A comparison of the solvolysis rates of the substituted 2‐__exo__‐ and 2‐__endo__ ‐norbornyl __p__‐toluenesulfonates **1, 2, 3** and **4** and the substituted 1‐ and 2‐adamantyl sulfonates **9** and **10**, respectively, in 80% ethanol and 97% trifluoroethanol has shown that the sensiti
Norbornanes. Part 18. Inductive Charge Dispersal in the Solvolyses of 4- and 5-Substituted 2-Norbornyl p-Toluenesulfonates
✍ Scribed by Francesco Fuso; Cyril A. Grob; Pawel Sawlewicz; Guo Wei Yao
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- German
- Weight
- 435 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
As measured by the pK, of 4-substituted quinuclidines [3] For the influence of 6-endo-substituents, see [2].
Derived from the equation log k = p,uy + log k,.
📜 SIMILAR VOLUMES
## Abstract The solvolysis rates and products of several 7‐__anti__‐substituted 2‐__endo__‐norbornyl __p__‐toluenesulfonates **11** have been determined and compared with those of the previously reported 6‐__exo__‐substituted 2‐__exo__‐norbornyl __p__‐toluenesulfonates **1.** Although the number of
## Abstract The solvolysis rate constants __k__ for the 6‐__endo__‐substituted 2‐__exo__‐norbornyl toluenesulfonates **7** have been determined. Values of log__k__ correlate well with the respective inductive constants of the substitutents except when the latter are nucleophilic and therefore lead
## Abstract The solvolysis rates and products of the 6__endo__‐R‐substituted 2__endo__‐norbornyl toluenesulfonates **6a**–**6i** have been determined. The rates of **6a**–**6g** correlate with the inductive constants σ the 6__endo__‐substituents and are not related to the size of the latter. It is
The solvolysis rates and products of the tertiary 2-methyl-2-exo-and -2-endonorbornyl 2,4-dinitrophenyl ethers 1 and 2, (X = 2,4-(NO,),C,H,O) have been determined. The different sensitivities of the rates of these ethers to the inductive effect of substituents at C(6) indicate that graded bridging o