Sigmatropic rearrangements antarafacial

Both suprafacial and antarafacial sigmatropic rearrangements are symmetry-allowed, but suprafacial rearrangements are often easier for geometric reasons. The rules for sigmatropic rearrangements are identical to those for cycJoaddition reactions (Table 30.3). 

The following reaction is an example of a [2,3] sigmatropic rearrangement. Would you expect the reaction to be supra facial or antarafacial Explain. 

An intramolecular rearrangement of the conjugate acid of the triazene compound to form the oc-complex without an additional molecule of amine would correspond to a thermal [l,3]-sigmatropic rearrangement. However, such a mechanism can be ruled out on the grounds of the antarafacial pathway required from orbital symmetry considerations (Woodward-Hoffmann rules). 

Sandmeyer reaction, 306 Sandwich compoimds, 275 Sawhorse projections, 7 Saytzev elimination, 249, 256 Schiff bases, 221 Schmidt rearrangement, 122 Selectivity, 156, 169, 326 a, 362 a, 370 372 aj,385 a bonds, 6 o complexes, 41,131 Sigmatropic rearrangements, 352-357 antarafacial, 353 carbon shifts, 354 hydrogen shifts, 352 orbital symmetry in, 352 photochemical, 354 suprafadal, 353 thermal, 353... 

A similar analysis of [1,5] sigmatropic rearrangements shows that in this case the thermal reaction must be suprafacial and the photochemical process antarafacial. For the general case, with odd-numbered /, we can say that [1,/] suprafacial migrations are allowed thermally when j is of the form 4n + 1, and photochemically when j has the form An - 1 the opposite is true for antarafacial migrations. 

Sigmatropic rearrangements in anions are more rare, but the isomerization of the conjugated anion 5.42 to the conjugated anion 5.45 probably takes place by a [1,6] shift 5.43 —> 5.44. It is known to be intramolecular, but the stereochemistry (antarafacial is allowed) could not be checked. In order for the reaction to take place at all, it is necessary for the stereochemistry within... 

The rules for [m,n -sigmatropic rearrangements, where m / 1 and n / I, are more complex still. The bond can migrate suprafacially or antarafacially on either component, with the great majority of known reactions being... 

Several cases of photochemical reactions, for which the thermal equivalents were forbidden, are shown below. In some cases the reactions simply did not occur thermally, like the [2 +2] and [4 +4] cycloadditions, and the 1,3- and 1,7-suprafacial sigmatropic rearrangements. In others, the photochemical reactions show different stereochemistry, as in the antarafacial cheletropic extrusion of sulfur dioxide, and in the electrocyclic reactions, where the 4-electron processes are now disrotatory and the 6-electron processes conrotatory. In each case,... 

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