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Like other chlorosilanes or silanes, silicon tetrachloride reacts readily with water: . SiCl 4 + 2 H 2 O → SiO 2 + 4 HCl. The reaction can be noticed on exposure of the liquid to air, as SiCl 4 vapour produces fumes as it reacts with moisture to give a cloud-like aerosol of silica and hydrochloric acid. [6]
VSEPR theory is used to predict the arrangement of electron pairs around central atoms in molecules, especially simple and symmetric molecules. A central atom is defined in this theory as an atom which is bonded to two or more other atoms, while a terminal atom is bonded to only one other atom.
As described by the VSEPR model, the five valence electron pairs on the central atom form a trigonal bipyramid in which the three lone pairs occupy the less crowded equatorial positions and the two bonded atoms occupy the two axial positions at the opposite ends of an axis, forming a linear molecule.
Std Gibbs free energy of formation, Δ f G o liquid: −619.8 kJ/mol Standard molar entropy, S o liquid: 239.7 J/(mol K) Heat capacity, c p: 145. J/(mol K) Gas properties Std enthalpy change of formation, Δ f H o gas: −657. kJ/mol Std Gibbs free energy of formation, Δ f G o gas: −617.0 kJ/mol Standard molar entropy, S o gas: 330.7 J/(mol ...
The geometry is common for certain main group compounds that have a stereochemically-active lone pair, as described by VSEPR theory. Certain compounds crystallize in both the trigonal bipyramidal and the square pyramidal structures, notably [Ni(CN) 5] 3−. [1]
This geometry is almost always consistent with VSEPR theory, which usually explains non-collinearity of atoms with a presence of lone pairs. There are several variants of bending, where the most common is AX 2 E 2 where two covalent bonds and two lone pairs of the central atom (A) form a complete 8-electron shell .
Square prismatic geometry (D 4h) is much less common compared to the square antiprism.An example of a molecular species with square prismatic geometry (a slightly flattened cube) is octafluoroprotactinate(V), [PaF 8] 3–, as found in its sodium salt, Na 3 PaF 8. [6]
Via hydrosilylation, trichlorosilane is a precursor to other useful organosilicon compounds: . RCH=CH 2 + HSiCl 3 → RCH 2 CH 2 SiCl 3. Some useful products of this or similar reactions include octadecyltrichlorosilane (OTS), perfluoroctyltrichlorosilane (PFOTCS), and perfluorodecyltrichlorosilane (FDTS).