Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Geometry trigonal planar

The hybridisation theory may be used to account for the direction of the bonds in an atom that is involved in three single bonds only, and which does not have any lone pairs. If the s orbital and only two of the three p orbitals are hybridised, leaving the pz orbital untouched, then three hybrid orbitals [Pg.62]

If these three orbitals are degenerate, what configuration relative to each other will they adopt These three orbitals will form a trigonal planar shape, with a bond angle of 120°. This leaves the last p orbital to project above and below the plane formed by the [Pg.62]

In the isolated molecule of boron trichloride, there are only three electron pairs around the boron, and so they adopt the trigonal planar geometry. The last orbital, pz, is left unused and so is an empty [Pg.63]

Again this is a trigonal planar species, with an empty orbital that projects above and below the plane of the C-H bonds. [Pg.63]

The trichloromethyl carbanion, CC13-, which is formed by the deprotonation of trichloromethane, CHCI3, may, under favourable conditions, lose a chloride anion. Write down the balanced equation [Pg.63]


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]

Valence shell electron-pair repulsion (VSEPR) model (Section 1.10) Method for predicting the shape of a molecule based on the notion that electron pairs surrounding a central atom repel one another. Four electron pairs will arrange themselves in a tetrahedral geometry, three will assume a trigonal planar geometry, and two electron pairs will adopt a linear arrangement. [Pg.1296]

Ball-and-stick model of triethylaluminum (a) and a stylized model (b) that emphasizes the trigonal planar geometry around the aluminum atom. [Pg.620]

Trigonal planar geometry Is common In carbon compounds that have double bonds. For example, ethylene has two trigonal planar carbon atoms. Each carbon atom has three ligands two hydrogen atoms and one CH2 group. [Pg.621]

Compounds like triethylaluminum and dimethylzinc that have metal-carbon bonds are rather uncommon. Nevertheless, trigonal planar geometry (.s and linear geometry (.S p) occur frequently in nature. As we show in Section 10-1. these geometries and their corresponding hybridizations occur in molecules with double bonds and triple bonds. [Pg.673]

C13-0116. The nitrogen atom of a peptide linkage has trigonal planar geometry. What is the hybridization of the nitrogen atom in a peptide linkage Explain why nitrogen adopts this form of hybridization. [Pg.970]

Trimethylboron is an example of one type of Lewis acid. This molecule has trigonal planar geometry in which the boron atom is s hybridized with a vacant 2 p orbital perpendicular to the plane of the molecule (Figure 21-11. Recall from Chapter 9 that atoms tend to use all their valence s and p orbitals to form covalent bonds. Second-row elements such as boron and nitrogen are most stable when surrounded by eight valence electrons divided among covalent bonds and lone pairs. The boron atom in B (CH ) can use its vacant 2 p orbital to form a fourth covalent bond to a new partner, provided that the new partner supplies both electrons. Trimethyl boron is a Lewis acid because it forms an additional bond by accepting a pair of electrons from some other chemical species. [Pg.1500]

The Gc2N2 ring of 53 is planar with both N atoms having a trigonal-planar geometry (359.97°) and in-plane arrangement of snbstitnents. In contrast, both Ge atoms are distinctly pyramidal (322.10°) with a markedly ont-of-plane tra i-arrangement of the aryl snbstitnents. [Pg.87]

In pyridine- X-C interactions, the C - X moiety is roughly coplanar with the pyridine and the two C-N- X angles are approximately 120° [129,143, 144]. The same holds for other nitrogen heteroaromatics (e.g. pyrazine, quinoline, etc.) [145-147]. A carbonyl group pins the donors after a trigonal planar geometry and works either as a mono- [148,149] or bidentate XB acceptor [150]. Sulfoxides behave similarly [151,152] and imines form XB along the expected axis of the lone pair [153]. [Pg.128]

It should be very important to reveal the structural features of heavy ketones and to make a systematic comparison with those of a carbonyl compound such as the bond shortening and the trigonal planar geometry which result from the sp2 hybridization between the carbon and oxygen atoms. [Pg.156]

Although some examples of thermodynamically stabilized double bond systems between Group 14 and Group 16 elements showed trigonal planar geometry due to their structural restriction, almost all of their bond lengths are longer than those kinetically stabilized and theoretically predicted.67 These results clearly show that considerable electronic perturbation is inevitably involved in the thermodynamically stabilized systems. [Pg.158]

In the molecule of 4-methylene-3-borahomoadamantane derivative 79, the structure of which was determined by X-ray analysis, the six carbon atoms of the triene system, the two boron and two silicon atoms all lie in one plane within experimental error (mean deviation 1.4 pm). The boron atoms deviate from the trigonal-planar geometry, since the sum of bond angles around the atoms is only 355.8° instead of 360°, as usually encountered in triorganoboranes. Considerable distortions of the bond angles at the terminal C-C double bond occurs in the vicinity of the boron atoms B-C(4)-C(ll) 130.60(19)° and B-C(4)-C(5) 107.38(17)° <2002CEJ1537>. [Pg.598]

Derivatives 80 and 81 have the same stereochemistry, indicating the deviation of the boron from trigonal-planar geometry into a pyramidal one (Table 5). [Pg.598]

It goes from a trigonal planar geometry and sp hybridization to a tetrahedral... [Pg.460]


See other pages where Geometry trigonal planar is mentioned: [Pg.1294]    [Pg.620]    [Pg.709]    [Pg.1509]    [Pg.88]    [Pg.88]    [Pg.266]    [Pg.266]    [Pg.284]    [Pg.55]    [Pg.66]    [Pg.67]    [Pg.68]    [Pg.69]    [Pg.82]    [Pg.87]    [Pg.16]    [Pg.20]    [Pg.39]    [Pg.202]    [Pg.206]    [Pg.20]    [Pg.489]    [Pg.916]    [Pg.920]    [Pg.952]    [Pg.979]    [Pg.1046]    [Pg.1149]    [Pg.1169]    [Pg.157]    [Pg.157]    [Pg.163]    [Pg.4]    [Pg.174]   
See also in sourсe #XX -- [ Pg.55 , Pg.89 , Pg.92 , Pg.98 ]

See also in sourсe #XX -- [ Pg.161 ]

See also in sourсe #XX -- [ Pg.223 , Pg.225 , Pg.226 ]

See also in sourсe #XX -- [ Pg.55 , Pg.56 , Pg.70 , Pg.73 , Pg.80 , Pg.82 , Pg.87 , Pg.157 , Pg.202 ]

See also in sourсe #XX -- [ Pg.333 , Pg.334 , Pg.335 , Pg.337 , Pg.343 , Pg.351 , Pg.1006 ]

See also in sourсe #XX -- [ Pg.107 ]

See also in sourсe #XX -- [ Pg.347 , Pg.348 , Pg.350 , Pg.357 , Pg.366 , Pg.1042 ]

See also in sourсe #XX -- [ Pg.15 ]

See also in sourсe #XX -- [ Pg.224 ]

See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.336 , Pg.338 ]

See also in sourсe #XX -- [ Pg.27 ]

See also in sourсe #XX -- [ Pg.133 , Pg.139 ]

See also in sourсe #XX -- [ Pg.37 , Pg.372 , Pg.386 ]




SEARCH



Coordination geometry trigonal planar

Electron geometry trigonal planar

Molecular geometry trigonal planar

Planar trigonal geometry, VSEPR

Three Electron Groups Trigonal Planar Geometry

Trigonal geometry

Trigonal planar

Trigonal planar geometry and VSEPR

Trigonal planar geometry and sp hybridization

Trigonal planar geometry and sp2 hybridization

Valence shell electron pair repulsion trigonal planar geometry

© 2024 chempedia.info