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Functional group relationships, and

As above, the log k values of the different types of compounds [alkanols (ROH), polycyclic aromatic hydrocarbons (PAH), alkyl benzenes (RB), and alkyl benzoates (ROB)] each demonstrated a linear relationship with their log P values and this relationship was observed with different ratios of acetonitrile and water. The experiment was then performed in eluents containing different organic modifiers and it was found that the behaviour of analytes containing different functional groups differed and the effect depended on the log P of the analyte. [Pg.59]

Carothers derived a relationship between the extent of reaction at the gel point and the average functionality /avg of the polymerization system for the case where the two functional groups A and B are present in equivalent amounts [Carothers, 1936]. The derivation follows in a manner similar to that for Eq. 2-78. The average functionality of a mixture of monomers is the average number of functional groups per monomer molecule for all types of monomer molecules. It is defined by... [Pg.105]

Figure 8 shows the relationships between the heat of adsorption and the polarizability of molecules for a homologous series of n-alkanes, ethers, and n-alcohols. AQspecific of the functional groups —O— and... [Pg.46]

This paper reports a study to verify the relationship between functional group distribution and thermal decomposition behavior. A Fourier transform infrared spectrometer (FTIR) has been employed to obtain quantitative infrared spectra of the coals, chars, and tars produced in the devolatilization experiments. The spectra have been deconvoluted by using a computerized spectral synthesis routine to obtain functional group distributions, which are compared to the model parameters. [Pg.96]

Suggest ways to make these two compounds. Show your disconnections and make sure you number the functional group relationships. [Pg.113]

Most reactions involving the enzymes listed in Section II include the combination of a carbanion center with an electrophilic center that is part of an un-symmetrical double bond, such as a carbonyl or imino function. The cases in which carbonium ion-type intermediates form involve a completely different structure. This is not a case of competing mechanisms among common functional groups, but rather a specific relationship between functional group structure and mechanism. [Pg.289]

This exercise affords students an opportunity to measure actual UV and FTIR absorption spectra of several organic solutes while comparing overall differences in UV and FTIR spectra for chemically similar and dissimilar organic solutes. The laboratory experiment focuses on the influence of delocalization of electron density and the nature of UV absorption spectra. The experiment also focuses on the relationship of organic functional group analysis and FTIR absorption spectra. A review of an appropriate text which reviews the theory of UV vis and FTIR absorption spectroscopy and molecular structure gives an appreciation of what will be observed in the laboratory (3). [Pg.549]

Other systems where substituent shift additivity fails include allylic alcohols and l,Y-unsaturated esters. The examples in Figure 4-4 illustrate these functional group relationships. The en-OTs that would result from simple addition of substituent effects can be seen by inspection. In these cases, as well as with the enone example, the direction of the effect can be explained as being the result... [Pg.51]

There is a simple test for this protocol. Is it possible to make molecule 1 by the reaction of the anion derived from 7 and acetone The answer is yes The lesson is to correlate disconnect fragments with real molecules. This often means recognizing the chemical relationships of the functional groups involved and adding appropriate functional group transformations. [Pg.1275]

Sometimes the orientation of two substituents m an aromatic compound precludes Its straightforward synthesis m Chloroethylbenzene for example has two ortho para directing groups m a meta relationship and so can t be prepared either from chloroben zene or ethylbenzene In cases such as this we couple electrophilic aromatic substitution with functional group manipulation to produce the desired compound... [Pg.505]


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Function relationships

Functional groups and

Functional relationships

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