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Quintuplets

The yield is determined by weighing the cold trap before and after distillation of methylenecyclopropane. Any small amounts of tetra-hydrofuran carried into the methylenecyclopropane trap are eliminated in a subsequent distillation. By proton magnetic resonance analysis the checkers found that no tetrahydrofuran reached the cold traps the spectrum (dichloromethane) shows a triplet at S 1.00 and a quintuplet at S 5.35 in the ratio 4 2. [Pg.39]

All results are based on the average of quintuplet samples. Cross-head speed = 200 mm/min. Pro-Struct adhesives are manufactured by Pro-Struct, Pinetown, South Africa. [Pg.250]

The proton resonance of 26 is also indicative of transannular interactions interspatial transannular coupling of each aromatic proton with all four fluorine nuclei of the other ring induces splitting of the aromatic protons (quintuplet r =3.18, /hf =0.8 Hz). An alternative... [Pg.86]

In order to simplify the problem we will 8issume that the state, , in which we are interested is singlet. Then, the 1-TRDM, linking to a quintuplet state vanishes. Therefore, the only cases that may arise come from singlet-singlet or singlet-triplet transitions. The cases that in principle have to be considered are ... [Pg.47]

The Problem Three years ago, the sum of the ages of the quintuplets and their older sister was 155. If Sis is five years older than her siblings, then how old are the quints today ... [Pg.206]

First, quintuplets refers to five siblings born at the same time. Designate the variable x as the age of the quints today. Their sister s age is then x + 5 years. Three years ago, the quints were x - 3 years old, and their sister was x + 5 - 3 or x + 2 years old. The sum of the ages of these six children is written by multiplying the quints age by five and adding the sister s age 5(x - 3) + (x + 2), and that sum is set equal to 155 for the equation. [Pg.207]

Polyradicals 6—8 in Scheme 8.3 further show the utility of the Ovchinnikov rule. For example, 2,4-dimethylenepentadienyl, 6, is immediately seen to have a quadruplet ground state, as well as 1,3,5-trimethylenebenzene, 7, while tripropadienemethyl, 8, is a quintuplet (Scheme 8.3). Many other examples are offered in Exercise 8.1. [Pg.227]

The reagent tris[3-t-butylhydroxymethylene)-D-camphorato]Eu(III) was used initially to separate the resonances of R and S enantiomeric amines [53]. The fluorinated reagent tris[3-trifluoroacetyl-D-camphorato]Eu(III), Eu(facam)3 was used in the separation of resonances of enantiomers of 2-phenyl-2-butanol. The spectra of 2-phenyl-2-butanol on addition of Eu(thd)3 and Eu(facam)3 are shown in Fig. 10.21. As seen in the figure, Eu(thd)3 did not cause changes in the resonances while Eu(facam)3 caused separation of a-methyl resonances into two peaks, and resolved the -methyl triplets into a quintuplet and thus distinguishing the two isomers [54],... [Pg.807]

Careful purification of solutions of fluorosilane and fluorosilicate anions and a decrease in concentration and temperature result in a fine structure of F NMR spectra due to a non-equivalent arrangement of ligands (Table 16). For example, in the F NMR spectra of octahedral complexes of the type RSiFj" a doublet (equatorial atoms) and a quintuplet are observed whose mutual arrangement depends on the nature of the ligand In fluorine derivatives of penta- or hexa-coordinate silicon with slow exchange, the Hgip values (if they can be determined) are greater for the fluorine atoms with chemical shifts in low field. [Pg.154]


See other pages where Quintuplets is mentioned: [Pg.83]    [Pg.61]    [Pg.254]    [Pg.169]    [Pg.172]    [Pg.172]    [Pg.296]    [Pg.265]    [Pg.265]    [Pg.146]    [Pg.288]    [Pg.94]    [Pg.26]    [Pg.47]    [Pg.131]    [Pg.518]    [Pg.219]    [Pg.223]    [Pg.231]    [Pg.202]    [Pg.597]    [Pg.173]    [Pg.174]    [Pg.188]    [Pg.195]    [Pg.227]    [Pg.252]    [Pg.252]    [Pg.190]   
See also in sourсe #XX -- [ Pg.1441 ]




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