ISSN:
1042-7163
Keywords:
Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
The mechanism of isomerization of allyl thiocyanate to allyl isothiocyanate has been investigated both experimentally and theoretically. The kinetic study indicates that the reaction is unimolecular and is not ionic. The entropy of activation suggests strongly that the mechanism involves a cyclic transition state. The rate of reaction was retarded to a small extent in polar solvents relative to that in nonpolar solvents. Ab initio MO calculations indicate, in agreement with the experimental results, that the reaction proceeds through a cyclic transition state, one in which the SCN moiety is almost linear. Thus, this is a [3,3] sigmatropic rearrangement. The charge separation in the transition state was substantial. The retardation of the reaction in polar solvents was attributed to the difference in solvation in the original state and in the transition state. © 1997 John Wiley & Sons, Inc.
Additional Material:
6 Ill.
Type of Medium:
Electronic Resource
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