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Single rings

The name naphthenic acid is derived from the early discovery of monobasic carboxyUc acids in petroleum, with these acids being based on a saturated single-ring stmcture. The low molecular weight naphthenic acids contain alkylated cyclopentane carboxyUc acids, with smaller amounts of cyclohexane derivatives occurring. The carboxyl group is usually attached to a side chain rather than direcdy attached to the cycloalkane. The simplest naphthenic acid is cyclopentane acetic acid [1123-00-8] (1, n = 1). [Pg.509]

For single rings (i.e. mononuclear systems) up to ten atoms in size, there is no question but that Hantzsch-Widman names are overwhelmingly the most widely used, and specialists can be presumed to recognize them readily. However, when one of the trivial names of Table 1 can be used, it prevails almost exclusively. Thiophene will be immediately understood by specialists and most nonspecialists, whereas thiole will distract the reader s attention from the chemistry while he considers the writer s intention is the Hantzsch-Widman system indeed being used, or is it a typographical error Chemical Abstracts also uses these trivial names in its indexes. [Pg.35]

Aromatics-single ring, mono and disubstituted by n-paraffins 6 1.91 0.0418 23.5 66.1... [Pg.360]

Aromatics-single ring, mono substituted by isoparaffins 2 2.99 0.0264 37.5 62.6... [Pg.360]

The barrier seals come in two basic forms. One is a labyrinth design, which is probably the most common. It has the features of a conventional labyrinth discussed earlier. The alternative is the carbon ring seal. The carbon ring is used either as a single ring or, in some cases, it is of a mui-... [Pg.219]

The preseparation utilized a 5 pim cyano column (250 cm X 4.6 mm i.d.) and a 5 p.m silica column (250 cm X 4.6 mm i.d.) in series, followed by GC analysis on an SE-54 column (25 m X 0.2 mm i.d., 0.33 p.m film thickness). The SFC system separated the aviation sample into two peaks, including saturates and single-ring aromatics as the first peak, and two-ring aromatic fractions as the second peak. These fractions were selectively cut and then transferred to the GC unit for further analysis. (Figure 12.20). [Pg.327]

Alkenes (Olefins) and Cycloalkenes. Olefins are unsaturated and highly reactive. Because of their propensity to be reduced to paraffins w ilh hydrogen or to merceptans with hydrogen sulfide, alkenes are found in petroleum only in very low concentrations. Single-ring cycloalkenes have the same formula, as olefins and so are difficult... [Pg.319]

Thomson based h(s configurations on the work of fin American physicist, Alfred Mayer, who had experimented wilh magnets attached to corks and floated In a circular basin of water. When five magnets were placed in the water, for example, they formed a single ring The ad-... [Pg.36]

The spiro monomers 57-59 are reported to give single ring-opening.27 5 27> Solution polymerization of 57m and 58 (R CH3, R C3H7) 4 provided soluble products. [Pg.208]

The Wittig reaction has been carried out intramolecularly, to prepare rings containing from 5 to 16 carbons, both by single ring closure... [Pg.1236]

After the components have been placed next to one another, drawing the final structure requires removal of the H2 O units. UMP has three components. From right to left in the drawing, they are uracil, a single-ring base ribose, the sugar and one phosphate group. [Pg.935]

When aromatics, even single-ring compoimds such as benzene, have one substituent already, the introduction of the next also gives rise to regioisomerism. In addition, the first one guides the introduction of the second by steric and electronic effects. [Pg.72]

Organic synthesis 33 [OS 33] Nitration of substituted single-ring aromatics... [Pg.450]

The nitration of several single-ring aromatics with two substituents at various ring positions has been reported [94], The exact nature of these species, however, was not disclosed, probably for intellectual property reasons, as the reactions were performed for an industrial company (BASF). [Pg.450]

OS 33] ]R 16h] [P 25] For the nitration of a single-ring aromatic in a capillary-flow micro reactor, experiments were performed at two temperature levels, 60 and 120 °C [94]. Owing to the assumed increase in conversion rate with higher temperature, attempts were made to compensate for this by decreasing the capillary length at otherwise constant dimensions. For the 60 °C experiment, a very low... [Pg.455]


See other pages where Single rings is mentioned: [Pg.395]    [Pg.1346]    [Pg.100]    [Pg.109]    [Pg.10]    [Pg.158]    [Pg.405]    [Pg.41]    [Pg.409]    [Pg.409]    [Pg.412]    [Pg.413]    [Pg.121]    [Pg.4]    [Pg.5]    [Pg.7]    [Pg.9]    [Pg.372]    [Pg.373]    [Pg.54]    [Pg.143]    [Pg.112]    [Pg.563]    [Pg.198]    [Pg.204]    [Pg.206]    [Pg.207]    [Pg.208]    [Pg.661]    [Pg.94]    [Pg.45]    [Pg.933]    [Pg.10]    [Pg.451]    [Pg.454]    [Pg.460]   
See also in sourсe #XX -- [ Pg.136 ]




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Aromatic compounds with single ring

Aromatics single-ring

Examples single ring

Hydrogenation single aromatic rings

Interconversion around the single bonds of rings

Saturated bicyclic 6/5 ring-fused systems with bridgehead nitrogen and a single

Saturated bicyclic 6/5 ring-fused systems with bridgehead nitrogen and a single additional

Single-Ring DBAs

Single-Ring Heterocyclic Sulfur Compounds

Single-rings, substituted

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