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Conformational mix

Biitene Now we shall look for the energies of the conformational mix of 1-bntene. We know less about this molecule than we did about /(-butane, so the procedure will be a lit.tle more complicated. [Pg.128]

Ahyd/7 of all the linear monoalkynes in this series were measured in n-hexane solution. The slight trend toward less exothermic enthalpies of hydrogenation for 2-octyne to 4-octyne is due to the larger number of conformers in the alkane product. Thus, A H of the alkyne is not decreasing along this series, Af H of the conformational mix of products is increasing. Compare the linear nonynes and decynes. [Pg.85]

Conformationally pure subset Conformationally mixed subset ... [Pg.750]

The behavior of this set of radial distribution functions and, conseqnently, the thermophysical properties of the system, are not compatible with the ideas underlying the popular vdW-lf conformal mixing rules. In fact, vdW-lf are based on the conformity of the radial distribution functions, that is,... [Pg.222]

Formulation consists of mixing the effluent streams coming from the different refining units in order to obtain products conforming to the specifications. It is also at this point that additives are added, the reasons for which and whose action will be described later. One can easily see that as far as octane numbers are concerned, or for that matter any other parameter, the... [Pg.202]

The temperature of esterification has a significant influence on isomerization rate, which does not proceed above 50% at reaction temperatures below 150°C. In resins produced rapidly by using propylene oxide and mixed phthaUc and maleic anhydrides at 150°C, the polyester polymers, which can be formed almost exclusively in the maleate conformation, show low cross-linking reaction rates with styrene. [Pg.315]

The separation of Hquid crystals as the concentration of ceUulose increases above a critical value (30%) is mosdy because of the higher combinatorial entropy of mixing of the conformationaHy extended ceUulosic chains in the ordered phase. The critical concentration depends on solvent and temperature, and has been estimated from the polymer chain conformation using lattice and virial theories of nematic ordering (102—107). The side-chain substituents govern solubiHty, and if sufficiently bulky and flexible can yield a thermotropic mesophase in an accessible temperature range. AcetoxypropylceUulose [96420-45-8], prepared by acetylating HPC, was the first reported thermotropic ceUulosic (108), and numerous other heavily substituted esters and ethers of hydroxyalkyl ceUuloses also form equUibrium chiral nematic phases, even at ambient temperatures. [Pg.243]

Real reactors may conform to some sort of ideal mixing patterns, or their performance may be simulated by combinations of ideal models. The commonest ideal models are the following ... [Pg.2083]

Figure 2.5 Schematic illustrations of antiparallel (3 sheets. Beta sheets are the second major element of secondary structure in proteins. The (3 strands are either all antiparallel as in this figure or all parallel or mixed as illustrated in following figures, (a) The extended conformation of a (3 strand. Side chains are shown as purple circles. The orientation of the (3 strand is at right angles to those of (b) and (c). A p strand is schematically illustrated as an arrow, from N to C terminus, (bj Schematic illustration of the hydrogen bond pattern in an antiparallel p sheet. Main-chain NH and O atoms within a p sheet are hydrogen bonded to each other. Figure 2.5 Schematic illustrations of antiparallel (3 sheets. Beta sheets are the second major element of secondary structure in proteins. The (3 strands are either all antiparallel as in this figure or all parallel or mixed as illustrated in following figures, (a) The extended conformation of a (3 strand. Side chains are shown as purple circles. The orientation of the (3 strand is at right angles to those of (b) and (c). A p strand is schematically illustrated as an arrow, from N to C terminus, (bj Schematic illustration of the hydrogen bond pattern in an antiparallel p sheet. Main-chain NH and O atoms within a p sheet are hydrogen bonded to each other.
It should be possible when walking through a machine shop, for example, to identify which products are awaiting inspection, which have been inspected and found conforming, and which have been rejected. If, by chance, some product were to become separated from its parent batch, it should still be possible to return the product to the location from whence it came. A machine shop is where this type of identification is essential - it is where mix-ups can occur. In other places, where mix-ups are unlikely, inspection and test identification does not need to be so explicit. [Pg.430]


See other pages where Conformational mix is mentioned: [Pg.125]    [Pg.126]    [Pg.128]    [Pg.151]    [Pg.153]    [Pg.158]    [Pg.142]    [Pg.260]    [Pg.750]    [Pg.752]    [Pg.759]    [Pg.191]    [Pg.226]    [Pg.539]    [Pg.125]    [Pg.126]    [Pg.128]    [Pg.151]    [Pg.153]    [Pg.158]    [Pg.142]    [Pg.260]    [Pg.750]    [Pg.752]    [Pg.759]    [Pg.191]    [Pg.226]    [Pg.539]    [Pg.157]    [Pg.493]    [Pg.494]    [Pg.126]    [Pg.345]    [Pg.108]    [Pg.167]    [Pg.263]    [Pg.411]    [Pg.298]    [Pg.544]    [Pg.545]    [Pg.469]    [Pg.300]    [Pg.482]    [Pg.447]    [Pg.310]    [Pg.436]    [Pg.438]    [Pg.233]   
See also in sourсe #XX -- [ Pg.126 , Pg.151 , Pg.152 ]




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Lipid mixed conformations

Mixed solvent influence on the conformer equilibrium

Mixing conformal solution

Three conformal solution mixing

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