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Benzene ortho-substituted

It is of interest that these reactions exhibit stronger activation of the substituent at C-5 by a neighboring electron-acceptor group compared with the corresponding ortho-substituted benzene. This is possibly owing either to the effect of the nitrogen hetero atom or to a weaker delocalization of multiple bonds in the heterocyclic nucleus. [Pg.391]

As might be expected, an increase in pressure reduces the selectivity of the nitronium ion (since the reactivity is effectively increased) and also increases the amount of ortho substitution this has been shown from the relative rates of nitration of benzene and /-butylbenzene in acetic acid at 45 °C60. [Pg.33]

Charton, M., Prog. Phys. Org. Chem., 8, 235 (1971) has reported extensively on correlations of rate data for ortho substituted benzene derivatives using the dual substituent parameter treatment in the form with an additional (intercept) parameter, and in our opinion, too limited substituent data sets. For these and related reasons which we have discussed, we question the significance of many of Charton s correlations. [Pg.80]

There is an obvious structural analogy between cw-vinylene sets, 1, and ortho-substituted benzene sets, 2. The possible existence of proximity effects in... [Pg.97]

These effects can occur when the active site at which a measurable phenomenon occurs is in close proximity to the substituent. Among the many systems exhibiting direct steric effects are ortho-substituted benzenes, 1, cis-substituted ethylenes, 2, and the ortho- (1,2-, 2,1- and 2,3-) and peri- (1,8-) substituted naphthalenes, 3, 4, 5 and 6, respectively. Other examples are d.v-1,2-disubstiUited cyclopropanes, c/ s-2,3-disubstituted norbornanes and ci.s-2,3-disubstituted [2.2.2]-bicyclooctanes, 7, 8 and 9, respectively. Some systems generally do not show steric effects. Vicinally substituted systems such as disubstituted methanes, 10, and 1,1-disubstituted ethenes, 11, are examples, 2,3-Disubstituted heteroarenes with five-membered rings such as thiophenes and selenophenes... [Pg.703]

Conveniently, ortho-substituted nitroso-benzenes prepared in a redox cell (vide supra) from the corresponding... [Pg.359]

In summary, the sulfonylureas are new herbicides which exhibit activity at extremely low rates of application and show very low mammalian toxicity. Exceptionally high activity is shown by compounds containing a benzene ring substituted in the ortho position, an unsubstituted sulfonylurea bridge, and a pyrimidine or triazine heterocycle substituted with methyl or methoxy groups. [Pg.28]

Conformational constraints induced by various ortho-substitutents in 1-aUyloxy-2-azidomethylbenzenes (97) were used to accelerate intramolecular cycloadditions of the azide group to alkenes (21) (Scheme 9.21). For the unsubstituted azide 96, high temperature was required for the cycloaddition and the yield of the cycloadduct 100 was low. The monosubstituted azide 97 underwent cycloaddition in refluxing benzene in 10 h to give the cycloadduct 101 in good yield. Disubstituted azides 98 and 99 underwent 1,3-dipolar cycloaddition in 5-7 h to give the triazolines 102 and 103. [Pg.634]

Fig. 12. End view of the geometry of an ortho-substituted benzene derivative. The X p group is variable, the planar bonded MZ Z2 group is constant... Fig. 12. End view of the geometry of an ortho-substituted benzene derivative. The X p group is variable, the planar bonded MZ Z2 group is constant...
Fig. 13. Top view of the geometry of an ortho-substituted benzene derivative... Fig. 13. Top view of the geometry of an ortho-substituted benzene derivative...
A somewhat related report in which equally impressive selectivity and yield (60—90%) were obtained Cacou and Wolf have studied the low temperature direct fluorination of aromatic compounds in CC13 F (100). They have established that under appropriate conditions molecular fluorination proceeds on substituted benzenes and tolulenes with similar selectivity and orientation as has been commonly observed for other halogens. For example reaction with nitrobenzene gives 80% meta substitution and reaction with tolulene gives 60% ortho substitution. The conversions were reported in this study and found to average 0.01%. [Pg.205]

Orthophthalic acid is made by the oxidation of naphthalene (1) with H2SCL fuming heated, in the presence of mercuric sulfate —SO2 is also formed and recovered (2 ) with air in the presence of vanadium pentoxide at 450 to 520°C. Orthophthalic acid also is formed when benzene compounds containing carbon ortho-substituted groups are oxidized. Orthophthalic arid is used in the manufacture of indigo and other dyes,... [Pg.1300]


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See also in sourсe #XX -- [ Pg.39 ]




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Benzene substitution

Disubstituted Benzenes Ortho, Meta, and Para Substitution

Ortho- Substitution

Substitution substituted benzenes

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