Cyclicality causes

Cyclic alkenes give different regioisomers depending on the reaction conditions owing to double bond isomerization caused by syii elimination of Pd—H species and its readdition. The following three reaction conditions were tested for the reaction of cycloheptene (35)[18,38] ... 

The pattern of orbital energies is different for benzene than it would be if the six tt electrons were confined to three noninteracting double bonds The delocalization provided by cyclic conjugation in benzene causes its tt electrons to be held more strongly than they would be in the absence of cyclic conjugation Stronger binding of its tt electrons is the factor most responsible for the special stability—the aromaticity—of benzene... 

In the X- and y-directions (Figure 49.5b), an ion trajectory is more difficult to visualize. It is essentially the sum of two main effects one a simple oscillation caused by the rapid cyclic alternations of the RF field (Figure 49.5c), the other a more complicated drift or guided motion due to the inhomogeneity of the RF field within the space between all four rods. 

Ton-exchange resins are used repeatedly in a cyclic manner over many years, and deterioration of both physical and chemical properties can be anticipated. Comparison of the properties of used resin with those of new resin is helpfiil to learning more about the nature and cause of deterioration (12). Corrective action frequendy extends the life of the resin. Comparison of properties must always be made with the resin in the same ionic form. 

In the oxaziridines (1) ring positions 1, 2 and 3 are attributed to oxygen, nitrogen and carbon respectively. The latter almost always is in the oxidation state of a carbonyl compound and only in rare cases that of a carboxylic acid. Oxaziridinones are not known. The nitrogen can be substituted by aryl, alkyl, H or acyl the substituent causes large differences in chemical behavior. Fused derivatives (4), accessible from cyclic starting materials (Section 5.08.4.1), do not differ from monocyclic oxaziridines. 

Under cyclic or repeated stress conditions, rupture of protective oxide films that prevent corrosion takes place at a greater rate than that at which new protec tive films can be formed. Such a situation frequently resiilts in formation of anodic areas at the points of rupture these produce pits that serve as stress-concentration points for the origin or cracks that cause ultimate failure. 

Small pits, some the size of pinheads, pockmarked surfaces (Fig. 7.22). Each pit was surrounded by a halo of reddish-brown rust. Cyclic wetting and evaporation caused chloride concentration and increased acidity locally. 

Several theories have been proposed to explain the corrosion-fatigue phenomena. One is that cyclic stressing causes repeated rupture of protective coatings. Corrosion-fatigue cracks propagate as the coating is successively reformed and ruptured along a plane. 

Hysteresis losses, caused by cyclic magnetization of steel. 

Additional cyclic torque. Caused by machining imperfections of drive components (particularly gearing) and imbalance of rotating drive components. 

Solving an indoor air quality problem is a cyclical process of data collection and hypothesis testing. Deeper and more detailed investigation is needed to suggest new hypotheses after any unsuccessful or partially-successful control attempt. Even the best planned investigations and mitigation actions may not produce a resolution to the problem. You may have made a careful investigation, found one or more apparent causes for the problem, and implemented a control system. Nonetheless,... 

Oxidation of tim5-4-(2,2,2-tnfluoro-l-hydroxy 1 tnfluoromethylethyl)cyclo-hexanol with pyridinium chlorochromate results m the correspondmg cyclic ketone whereas oxidation with nitnc acid m the presence of a catalyst causes ring cleavage [50] (equation 46)... 

Irradiation of cyclic ketones having perfluoroalkyl groups causes cleavage of a ring to yield acyclic products [I74 (equation 44) Similarly, perfluonnated ketones undergo decarbonylation when irradiated [775]. Gas-phase photolysis of perfluorodiazoketones, in the presence of a trapping agent, yields fluorinated furan as a major product [176] (equation 45)... 

In contrast to other acids, anhydrous hydrogen fluoride does not cause hydroly SIS and decarboxylation of the malonic acid residues in these reactions [5]. It is a good reagent for the cyclization of a-benzamidoacetophenones to 2,5 diphenyl-oxazoles [6] (equation 7) The same reaction with concentrated sulfuric acid gives cyclic product with only a 12% yield [6]... 

The cyclic thioketone, 3-oxotctrahydrothiophene (11), gives a mixture of enamines (12,13) when caused to react with a secondary amine such as piperidine or pyrrolidine (31). The enamine mixture can be reduced to the 3-aminotetrahydrothiophene using formic acid or oxidized to the 3-amino-thiophene using diisopentylsulfide. 

If cyclic ketones are monosubstituted in the a-position, their rates of reaction decrease as compared to the rate for the parent ketone (9,41). More highly substituted ketones (e.g., diisobutyl ketone, diisopropyl ketone) can be caused to react using newer preparative techniques (39,43,44, see Section VII). Monosubstituted acetones often can give selfcondensation products, but the recent literature (13,39,43) contains reports of the successful formation of the enamines of methyl ketones. 

---