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Stick figure forms

Double and triple bonds are represented with bent bonds formed with flexible couplings. Substances that require models with bent bonds normally are found to be much less stable and, therefore, chemically more reactive than molecules which can be constructed with straight sticks. Figure 1-4 shows the double bond of ethylene, the triple bond of acetylene, and the distorted bonds of cyclopropane. [Pg.10]

Models of ethene and methanal can be built with ball-and-stick models by using flexible couplings or bent sticks to form the double bonds (Figure 2-2), but the H—C—H angles are inaccurate because they are 109.5° rather than the observed 117° to 118°. [Pg.35]

For fine powders that tend to bridge or stick and are of low bulk density, some form of forced feed, such as the tapered screw feeder shown in Figure 9, must be used to deaerate, precompact, and pressurize the feed into the nip. Large machines are available with up to five screw feeders to spread the flow across the roUs, and vacuum hoppers are also used to remove air when densifying low density feeds. [Pg.117]

Figure 14.1 Each polypeptide chain in the collagen molecule folds into an extended polyproline type II helix with a rise per turn along the helix of 9.6 A comprising 3.3 residues. In the collagen molecule three such chains are supercoiled about a common axis to form a 3000-A-long rod-like molecule. The amino acid sequence contains repeats of -Gly-X-Y- where X is often proline and Y is often hydroxyproline. (a) Ball and stick model of two turns of one polypeptide chain. Figure 14.1 Each polypeptide chain in the collagen molecule folds into an extended polyproline type II helix with a rise per turn along the helix of 9.6 A comprising 3.3 residues. In the collagen molecule three such chains are supercoiled about a common axis to form a 3000-A-long rod-like molecule. The amino acid sequence contains repeats of -Gly-X-Y- where X is often proline and Y is often hydroxyproline. (a) Ball and stick model of two turns of one polypeptide chain.
Figure Three represernarions of the structure of Cm- (a) normal ball-and-stick model (b) the polyhedron derived by truncating the 12 vertices of an icosahedron to form 12 symmetrically separated pentagonal faces (c) a conventional bonding model. Figure Three represernarions of the structure of Cm- (a) normal ball-and-stick model (b) the polyhedron derived by truncating the 12 vertices of an icosahedron to form 12 symmetrically separated pentagonal faces (c) a conventional bonding model.
The filaments of all plant fibers consist of several cells. These cells form crystalline microfibrils (cellulose), which are connected together into a complete layer by amorphous lignin and hemi-cellulose. Multiple layers stick together to form multiple layer composites, filaments. A single cell is subdivided into several concentric layers, one primary and three secondary layers. Figure 5 shows a jute cell. The cell walls differ in their composition and in the orientation of the cellulose microfibrils whereby the characteristic values change from one natural fiber to another. [Pg.793]

FIGURE H.3 When methane burns, it forms carbon dioxide and water. The blue color is due to the presence of C2 molecules in the flame. If the oxygen supply is inadequate, these carbon molecules can stick togelher and form soot, thereby producing a smoky flame. Note that one carbon dioxide molecule and two water molecules are produced for each methane molecule that is consumed. The two hydrogen atoms in each water molecule do not necessarily come from the same methane molecule the illustration depicts the overall outcome, not the specific outcome of the reaction of one molecule. The excess oxygen remains unreacted. [Pg.87]

FIGURE 5.11 The viscosities of several liquids. Liquids com K>sed of molecules that cannot form hydrogen I Kinds are generally less viscous than those that can form hydrogen bonds. Mercury is an exception its atoms stick together by a kind of metallic bonding, and its viscosity is very high. The centipoise (cP) is the unit commonly used to report viscosity (1 cP = 10 1 kg-m-s ). [Pg.308]

Stimulated by these observations, Odelius et al. [73] performed molecular dynamic (MD) simulations of water adsorption at the surface of muscovite mica. They found that at monolayer coverage, water forms a fully connected two-dimensional hydrogen-bonded network in epitaxy with the mica lattice, which is stable at room temperature. A model of the calculated structure is shown in Figure 26. The icelike monolayer (actually a warped molecular bilayer) corresponds to what we have called phase-I. The model is in line with the observed hexagonal shape of the boundaries between phase-I and phase-II. Another result of the MD simulations is that no free OH bonds stick out of the surface and that on average the dipole moment of the water molecules points downward toward the surface, giving a ferroelectric character to the water bilayer. [Pg.274]

The pump in Figure 80, /, pumps at every other stroke, because one stroke is required to fill the chamber between the valves. A. H. CocKETT (1955) describes the piunp shown in Figure 80, III, which pumps at every stroke. The piston P consists of a magnet encased in polythene—tl avoids trouble which can arise from a glass piston in a glass tube forming powdered glass so that the piston sticks. It is... [Pg.180]

Figure 17.3 Anatomy of a redox enzyme representation of the X-ray crystallographic structure of Trametes versicolor laccase III (PDB file IKYA) [Bertrand et al., 2002]. The protein is represented in green lines and the Cu atoms are shown as gold spheres. Sugar moieties attached to the surface of the protein are shown in red. A molecule of 2,5-xyhdine that co-crystallized with the protein (shown in stick form in elemental colors) is thought to occupy the broad-specificity hydrophobic binding pocket where organic substrates ate oxidized by the enzyme. Electrons from substrate oxidation are passed to the mononuclear blue Cu center and then to the trinuclear Cu active site where O2 is reduced to H2O. (See color insert.)... Figure 17.3 Anatomy of a redox enzyme representation of the X-ray crystallographic structure of Trametes versicolor laccase III (PDB file IKYA) [Bertrand et al., 2002]. The protein is represented in green lines and the Cu atoms are shown as gold spheres. Sugar moieties attached to the surface of the protein are shown in red. A molecule of 2,5-xyhdine that co-crystallized with the protein (shown in stick form in elemental colors) is thought to occupy the broad-specificity hydrophobic binding pocket where organic substrates ate oxidized by the enzyme. Electrons from substrate oxidation are passed to the mononuclear blue Cu center and then to the trinuclear Cu active site where O2 is reduced to H2O. (See color insert.)...
Figure 4.14 (a) The boat conformation of cyclohexane is formed by "flipping" one end of the chair form up (or down). This flip requires only rotations about carbon-carbon single bonds, (b) Ball-and-stick model of the boat conformation, (c) A space-filling model. [Pg.156]

The psoralen ring system can intercalate within double-stranded DNA or RNA and induce the formation of adducts with adjacent thymine bases (Figure 11.15). The furan-side and pyrone-side of the tricyclic rings in psoralen both can form cycloaddition products with the 5,6-double bond of thymine residues, which results in crosslinks between the DNA strands with a PEG-biotin label sticking out. [Pg.533]

FIGURE 5-11 Ribbon diagram of an NBD dimer (PDB 160). 3 strands are depicted as arrows and a helices as coiled ribbons. The two nucleotides, shown as stick models, bind to form part of the interface that stabilizes the dimeric interaction. (With permission from Fig. 5 of reference [88].)... [Pg.83]


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