A 1,2-rearrangement

Reactive scattering or a chemical reaction is characterized by a rearrangement of the component particles within the collision system, thereby resulting in a change of the physical and chemical identity of the original collision reactants A + B into different collision products C + D. Total mass is conserved. The reaction is exothemiic when rel(CD) > (AB) and is endothermic when rel(CD) < (AB). A threshold energy is required for the endothemiic reaction. 

Note 1. At higher temperatures the tertiary chloride undergoes a rearrangement, catalysed by CuCl, giving H2C=C(C1)CH=CH2. In these cases the refractive index of the crude product is much higher. 

When fragmentation is accompanied by the formation of a new bond as well as by the breaking of an existing bond, a rearrangement process is involved. These will be even mass peaks when only C, H, and O are involved. The migrating atom is almost exclusively hydrogen six-membered cyclic transition states are most important. 

In a curve-fitting method the concentration of a reactant or product is monitored continuously as a function of time, and a regression analysis is used to fit an appropriate differential or integral rate equation to the data. Eor example, the initial concentration of analyte for a pseudo-first-order reaction, in which the concentration of a product is followed as a function of time, can be determined by fitting a rearranged form of equation 13.12... 

Heating triacetylboron at temperatures above its melting poiat, 123°C, causes a rearrangement to B20(0CCH2)4 (15). An explosive hazard is also generated by dissolving BF ia anhydride (see Boron compounds). 

Alternatively, a number of investigators (69—73) have proposed, on the basis of plausible kinetic arguments, that the conjugate olefin is produced by a rearrangement of alkylperoxy radicals (eq. 24). 

Extended x-ray absorption fine stmcture measurements (EXAFS) have been performed to iavestigate the short-range stmcture of TbFe films (46). It is observed that there is an excess number of Fe—Fe and Tb—Tb pairs ia the plane of the amorphous film and an excess number of Tb—Fe pairs perpendicular to film. The iacrease of K with the substrate temperature for samples prepared by evaporation is explained by a rearrangement of local absorbed atom configurations duting the growth of the film (surface-iaduced textuting) (47). 

With secondary amines such as piperidine or dimethylamine the formal products (169) of cine substitution are obtained with primary amines e.g. /-butylamine), in addition to the displacement product (173), a rearranged product (174) is obtained in which the nitrogen-bearing methyl becomes exocyclic 80CC123). Earlier studies on the reaction of... 

Nitrobenzofuroxan (355) undergoes a rearrangement (recognizable as an isomerization in unsymmetrically substituted derivatives) which is an example of this general rearrangement (Scheme 45) (64AG(E)693) see Table 10. 

Whereas the cycloaddition of arylazirines with simple alkenes produces A -pyrrolines, a rearranged isomer can be formed when the alkene and the azirine moieties are suitably arranged in the same molecule. This type of intramolecular photocycloaddition was first detected using 2-vinyl-substituted azirines (75JA4682). Irradiation of azirine (54) in benzene afforded a 2,3-disubstituted pyrrole (55), while thermolysis gave a 2,5-disubstituted pyrrole (56). Photolysis of azirine (57) proceeded similarly and gave 1,2-diphenylimidazole (58) as the exclusive photoproduct. This stands in marked contrast to the thermal reaction of (57) which afforded 1,3-diphenylpyrazole (59) as the only product. 

Fouling Fouling affec ts MF as it affects all membrane processes. One difference is that the fouling effect caused by deposition of a foulant in the pores or on the surface of the membrane can be confounded by a rearrangement or compression of the sohds cake which may form on the membrane surface. Also, the high, open space found in tortuous-pore membranes makes them slower to foiil and harder to clean. 

Careful watching is necessary at this point, since if the distillation is carried too far a violent reaction, apparently a rearrangement of the initial addition product may set in. 

Figure 4.6 The bifunctional enzyme PRA-isomerase (PRAI) IGP-synthase (IGPS) catalyzes two sequential reactions in the biosynthesis of tryptophan. In the first reaction (top half), which is catalyzed by the C-terminal PRAI domain of the enzyme, the substrate N-(5 -phosphoribosyl) anthranilate (PRA) is converted to l-(o-carboxyphenylamino)-l-deoxyribulose 5-phosphate (CdRP) by a rearrangement reaction. The succeeding step (bottom half), a ring closure reaction from CdRP to indole-3-glycerol phosphate (IGP), is catalyzed by the N-terminal IGPS domain.

In the discussion so far, an ideal termination of the bulk crystal has been assumed at the surface that is, the positions of atoms in the surface have been assumed to be the same as what they would have been in the bulk before the surface was created. This may not be true. Reconstruction, a rearrangement of atoms in the surfrce and near-surface layers, occurs frequently. It is caused by an attempt of the surface to lower its free energy by eliminating broken bonds. The atomic layers par-... 

In turn the oxazoline-containing polymer may then react very rapidly (e.g. at 240°C) with such groups as carboxyls, amines, phenols, anhydrides or epoxides, which may be present in other polymers. This reaction will link the two polymers by a rearrangement reaction similar to that involved in a rearrangement polymerisation without the evolution of water or any gaseous condensation products (Figure 7.14). 

Such reactions allow chain extension and/or cross-linking to occur without the elimination of small molecules such as water, i.e. they react by a rearrangement polymerisation type of reaction. In consequence these materials exhibit a lower curing shrinkage than many other types of thermosetting plastics. 

In contiaat, die isomer, in which tire double bond is not in a position to participate in die iooizsdon step, reacts 10 times slower than die anti isomer. The reaction product is derived fiom a rearranged caibocation ion that is stabilized by virtue of being allylic. ... 

Dehydrotestosterone acetate (174) in nonprotic solvents (dioxane, benzene) undergoes a rearrangement to the isomer (175). This product is photolabile and isomerizes readily to new cross-conjugated dienones. Thus, ultraviolet irradiation of (174), its 1-, 2- and 4-methyl homologs, and its lOa-stereoisomer (188) in dioxane solution causes, in each case, a series of rearrangements as summarized on page 331 for (174) and (188). ... 

Reaction of A with water under kinetic control conditions leads to the 5)5,19-cyclo-6 -ol (69a), whereas under conditions of thermodynamic control A rearranges to the isomeric cation B which reacts with water to give the B-homo-7)5-ol (70a). 

Contracted notation is a rearrangement of terms such that the number of indices is reduced although their range increases. For second-order tensors, the number of indices is reduced from 2 to 1 and the range increased from 3 to 9. The stresses and strains, for example, are contracted as in Table A-1. Similarly, the fourth-order tensors for stiffnesses and compliances in Equations (A.42) and (A.43) have 2 instead of 4 free indices with a new range of 9. The number of components remains 81 (3 = 9 ). 

Fluonnation of a ketone, 4-protoadamantanone, with sulfur tetrafluoride gives a 93 yield of a rearrangement product, 1,2-difluoroadamantane [173] (equation 88)... 

Strong acids or superacid systems generate stable fluorinated carbocations [40, 42] Treatment of tetrafluorobenzbarrelene with arenesulfonyl chlorides in nitro-methane-lithium perchlorate yields a crystalline salt with a rearranged benzo barrelene skeleton [43] Ionization of polycyclic adducts of difluorocarbene and derivatives of bornadiene with antimony pentafluonde in fluorosulfonyl chloride yields stable cations [44, 45]... 

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