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Trigonal bonding

Figure 7.12 (a) Part of a layer of Al(OH)3 (idealized) the heavy and light open circles represent OH groups above and below the plane of the A1 atoms. In a-Al(OH)3 the layers are stacked to give approximately hep. (b) Structure of y-Al(OH)3 viewed in a direction parallel to the layers the OH groups labelled C and D are stacked directly beneath A and B. The six OH groups A, B, C, D and B, D (behind B and D), form a distorted H-bonded trigonal prism. [Pg.245]

If back donation occurs to a ligand, the flow of electron density from the metal leaves less electron density to be donated in the opposite direction. It seems that this should have little effect on the donation of a pair of electrons on the ligand in the trans position to form a a bond. Accordingly, the major factor appears to be the stabilization of a five-bonded (trigonal bipyramid) transition state as a result of 7r bond formation. Ligands that readily form 1r bonds include some of those that generate the largest trans effect. [Pg.724]

In silicon derivatives, X-ray studies of compound 27 were consistent with a covalently bonded trigonal bipyramidal molecule <2000CC565>. In addition, nucleophilic substitution at silicon for similar compounds was modeled either by NMR or X-ray techniques and both methods correlate in the calculation of % Si-O bond formation <2003JOM66, 2003JOM154>. [Pg.593]

Molecular Geometry Tetrahedral with four atoms bonded. Trigonal pyramidal with three atoms bonded. Bent with two atoms bonded. Trigonal planar with three atoms bonded. Linear with two atoms bonded. [Pg.70]

Keywords Hypervalency, Sulfurane, Persulfonium salt, Persulfurane, Ligand exchange reaction, Ligand coupling reaction, Pseudorotation, Apical bond, Equatorial bond, Trigonal bipyrami-dal, Octahedral, Three-center four-electron bond... [Pg.89]

Carbon s Ability to Form Double and Triple Bonds Carbon atoms also form double bonds (trigonal planar geometry) and triple bonds (linear geometry), adding even more diversity to the number of compounds that carbon forms. [Pg.952]

Both these molecules exist in the gaseous state and both are trigonal planar as indicated by reference to Table 2.8. However, in each, a further covalent bond can be formed, in which both electrons of the shared pair are provided by one atom, not one from each as in normal covalent bonding. For example, monomeric aluminium chloride and ammonia form a stable compound ... [Pg.41]

The formation of a fourth covalent bond by the aluminium atom results in spatial rearrangement from the trigonal planar, for three bonding electron pairs, to tetrahedral, for four bonding electron pairs. [Pg.41]

As in the case of NH4 the charge is distributed over the whole ion. By considering each multiple bond to behave spatially as a single bond we are again able to use Table 2.8 to correctly deduce that the carbonate ion has a trigonal planar symmetry. Structures for other covalently-bonded ions can readily be deduced. [Pg.44]

The element before carbon in Period 2, boron, has one electron less than carbon, and forms many covalent compounds of type BX3 where X is a monovalent atom or group. In these, the boron uses three sp hybrid orbitals to form three trigonal planar bonds, like carbon in ethene, but the unhybridised 2p orbital is vacant, i.e. it contains no electrons. In the nitrogen atom (one more electron than carbon) one orbital must contain two electrons—the lone pair hence sp hybridisation will give four tetrahedral orbitals, one containing this lone pair. Oxygen similarly hybridised will have two orbitals occupied by lone pairs, and fluorine, three. Hence the hydrides of the elements from carbon to fluorine have the structures... [Pg.57]

Carbon symmetry -letraheJnil isp ) C -C bond length 15.4 nm. trigonal planar sp ) C C bond length 14.2 nm interplanar distance 3J.5 nm... [Pg.163]

The carbon atoms of the double bond have a trigonal planar configuration and free rotation about the C—C bond is prevented by the n bond. The inability to rotate means that geometrical isomers can be produced, with substituents a and b, thus ... [Pg.173]

To ensure that the arrangement of four atoms in a trigonal planar environment (e.g., a sp -hybridized carbon atom) remains essentially planar, a quadratic term like V(0) = (fe/2) is used to achieve the desired geometry. By calculating the angle 9 between a bond from the central atom and the plane defined by the central... [Pg.343]

The coefficients C are chosen to ensure that the function has a minimum at the appropriate reference bond angle. For linear, trigonal, square planar and octahedral coordination, Fourier series with just two terms are used with a Cq term and a term for n = 1, 2, 3 or 4, respectively ... [Pg.253]

Ammonia (NH3) 107 H / Nitrogen has three bonded pairs + one unshared pair Tetrahedral Trigonal pyramidal ... [Pg.30]

Boron trifluoride (BF3) F 20. B- F F Boron has three bonded pairs Trigonal planar Trigonal planar ... [Pg.30]

Boron trifluoride is a trigonal planar molecule There are six electrons two for each B—F bond associated with the valence shell of boron These three bonded pairs are farthest apart when they are coplanar with F—B—F bond angles of 120°... [Pg.31]

Multiple bonds are treated as a single unit m the VSEPR model Formaldehyde is a trigonal planar molecule m which the electrons of the double bond and those of the two single bonds are maximally separated A linear arrangement of atoms m carbon diox ide allows the electrons m one double bond to be as far away as possible from the elec Irons m the other double bond... [Pg.31]

Physical Properties. Sulfur tetrafluoride has the stmcture of a distorted trigonal bipyramid, the sulfur having hybrid sp d orbitals and an unshared electron pair (93). The FSF bond angles have been found to be 101° and 187°, and the bond distances 0.1646 and 0.1545 nm (94). [Pg.243]

The chemistry of propylene is characterized both by the double bond and by the aHyUc hydrogen atoms. Propylene is the smallest stable unsaturated hydrocarbon molecule that exhibits low order symmetry, ie, only reflection along the main plane. This loss of symmetry, which implies the possibiUty of different types of chemical reactions, is also responsible for the existence of the propylene dipole moment of 0.35 D. Carbon atoms 1 and 2 have trigonal planar geometry identical to that of ethylene. Generally, these carbons are not free to rotate, because of the double bond. Carbon atom 3 is tetrahedral, like methane, and is free to rotate. The hydrogen atoms attached to this carbon are aUyflc. [Pg.124]


See other pages where Trigonal bonding is mentioned: [Pg.528]    [Pg.273]    [Pg.282]    [Pg.313]    [Pg.507]    [Pg.333]    [Pg.1174]    [Pg.347]    [Pg.635]    [Pg.71]    [Pg.183]    [Pg.372]    [Pg.528]    [Pg.273]    [Pg.282]    [Pg.313]    [Pg.507]    [Pg.333]    [Pg.1174]    [Pg.347]    [Pg.635]    [Pg.71]    [Pg.183]    [Pg.372]    [Pg.2396]    [Pg.39]    [Pg.152]    [Pg.164]    [Pg.251]    [Pg.252]    [Pg.316]    [Pg.916]    [Pg.180]    [Pg.159]    [Pg.24]    [Pg.72]    [Pg.73]    [Pg.358]    [Pg.358]    [Pg.384]   
See also in sourсe #XX -- [ Pg.31 , Pg.36 , Pg.37 , Pg.38 , Pg.39 , Pg.40 , Pg.97 , Pg.243 , Pg.582 , Pg.761 ]




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