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FRAMs

Parcelain Made fram clays hydraus Electrical insulatars. [Pg.163]

Dimethylpentane Isopropyl benzene fraMS-2-Pentene 1,2,4-Trimethylbenzene... [Pg.169]

FIGURE iO.45 Capture of lime dust fram a clamshell unloading operation (three regions of lime drop flow patterns are modeled). [Pg.907]

Conjugated, cross-conjugated, and homoconjugated fluoroalkenes react with halogens to yield predominantly 1,4-adducts Results from the reactions of a series of conjugated fluoroalkenes with elemental halogens are summarized in Table 4 In nearly all cases, the fraMs-l,4-addition products are formed exclusively [Il ... [Pg.367]

Suggest an efficient synthesis of fram-2-heptene from propyne ] and any necessary organic or inorganic reagents. I... [Pg.376]

Problem 4.20 Which isomer is more stable, c/s-decalin or fram-decalin Explain. [Pg.129]

Using the relationship between equilibrium constant and free energy shown previously in Figure 4.12, p. 122, we can calculate that ds-2-butene is less stable than fram-2-butene by 2.8 kj/mol (0.66 kcal/mol) at room temperature. [Pg.185]

In step 8 of fatty-acid biosynthesis (Figure 29.5), reduction of fram-crotonyl ACP gives butyryl ACP. A hydride from NADPH adds to C3 of the crotonyl group from file Re face, and protonation on C2 occurs on the Si face. Is tire reduction a syn addition or an anti addition ... [Pg.1175]

Figure 4-1. Chemical slruclure of (I) fram-polyaceiylene (II) poly(/wra-phcnylenc vinylcne) (III) poly(/>ara-phenylcnc) (IV) polylhiophcne and (V) poiyanilincs. Figure 4-1. Chemical slruclure of (I) fram-polyaceiylene (II) poly(/wra-phcnylenc vinylcne) (III) poly(/>ara-phenylcnc) (IV) polylhiophcne and (V) poiyanilincs.
Acetic acid, fram-cyclohexanediaminetetra-metal complexes, 1,554... [Pg.74]

Consider a sample with two fluorophores, A and B, whose lifetimes (lA and XB) are each independent of emission wavelength and are different fram one another. By setting 4>D = 4>A 90°, the contribution from A is nulled out and the scanned emission spectrum represents only the contribution from B. Similarly, the spectrum for A is obtained by setting 4>D = 4>B 90°. In practice, finding the correct value of for this... [Pg.200]

Heiserman JE, Drayer BP, Keller PJ, Fram EK. Intracranial vascular stenosis and occlusion evaluation with three-dimensional time-of-flight MR angiography. Radiology 1992 185 667-673. [Pg.32]

Memory) (128 KB) on the MIMOSII electronics board. Firmware parameters and the instrument logbook are stored in the nonvolatile memory ferroelectric RAM (FRAM) on the electronics board. There are three individual FRAMs on the MIMOS II electronics board with three identical copies of these parameters to ensure parameter integrity. The copies are compared with each other from time to time to verify that they are identical. If one copy deviates from the other two, it is replaced by a copy of the other two identical parameter sets. All parameters can be adjusted during mission operations. [Pg.66]

It is of interest to investigate the usefulness of this theory to the chemical change involving the interaction between the conjugated systems 56,62,145). Such a-n interactions are frequently stereoselective. The addition to olefinic double bonds and the a, -elimination are liable to take place with the fraMS-mode 146h The Diels-Alder reaction occurs with the cis-fashion with respect to both diene and dienophile. [Pg.73]

These reactions, while not very important for high-energy donors in the absence of azulene, do help define what the potential energy diagrams should look like, that is, the fram-stilbene triplet is a discrete intermediate while the cij-stilbene triplet is a high vibrational form of the phantom triplet. Herkstroeter and McClure(13> have been able to observe the fro/w-stilbene triplet via flash photolysis using low-temperature glasses however, no similar triplet was observed for cfr-stilbene. Only when they studied cfr-stilbene-like... [Pg.193]

In total the analysis of protein complexes indicates that methionine is the most likely group to bind to [PtCU]2 and [PtenClfc] probably by a displacement reaction. However a specific attachment to another residue such as histidine or sulphydryl can not be ruled out. Furthermore the antitumour activity is that of cis- [Pt (NH 3) 2CI2] and the di-functional character of this reagent has not been revealed so far by the above studies. In fact no attempt has been made to uncover the difference between [PtCl2(NH3)2] in its cis and fraMS-forms. [Pg.37]

Gottlieb, A.G., Fram, D.M., Whitehead, S.F., Rubin, G.M., Russell, C.H., Castleman, P.A., Webb, F.N., "CLINFO A Friendly Computer System for Clinical Research", XII International Conference on Medical and Biomedical Engineering, Jerusalem, Israel, 1979. [Pg.30]

Attempts to react the oxidant with fram-dichlorocthylene or tetrafluoroethylene at ambient temperature in absence of diluent caused violent explosions. The oxidant should not be allowed to contact organic or easily oxidised material without adequate precautions. [Pg.144]


See other pages where FRAMs is mentioned: [Pg.190]    [Pg.198]    [Pg.263]    [Pg.233]    [Pg.233]    [Pg.649]    [Pg.728]    [Pg.1013]    [Pg.1261]    [Pg.96]    [Pg.53]    [Pg.898]    [Pg.898]    [Pg.404]    [Pg.2418]    [Pg.84]    [Pg.99]    [Pg.139]    [Pg.454]    [Pg.455]    [Pg.494]    [Pg.9]    [Pg.265]    [Pg.273]    [Pg.273]    [Pg.226]    [Pg.206]    [Pg.233]    [Pg.331]    [Pg.332]    [Pg.361]    [Pg.443]    [Pg.30]   
See also in sourсe #XX -- [ Pg.569 ]

See also in sourсe #XX -- [ Pg.569 ]




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Fram Strait

Fram-Diols

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