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4 Vapor pressure of liquid. 5 Spectral data. 6 References. ... This page provides supplementary chemical data on toluene. MSDS sheets. Structure and properties
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Toluene is also found in cigarette smoke and car exhaust. If not in contact with air, toluene can remain unchanged in soil or water for a long time. [39] Toluene is a common solvent, e.g. for paints, paint thinners, silicone sealants, [40] many chemical reactants, rubber, printing ink, adhesives (glues), lacquers, leather tanners, and ...
The Antoine equation is = +. where p is the vapor pressure, T is temperature (in °C or in K according to the value of C) and A, B and C are component-specific constants.. The simplified form with C set to zero:
Negative azeotropes are also called maximum boiling mixtures or pressure minimum azeotropes. An example of a negative azeotrope is hydrochloric acid at a concentration of 20.2% and 79.8% water (by mass). Hydrogen chloride boils at −85 °C and water at 100 °C, but the azeotrope boils at 110 °C, which is higher than either of its constituents.
For ring closing reactions, it is an example of enantioselectivity, wherein a single enantiomer of a cyclization product is formed from the selective ring closure of the starting material. In a typical electrocyclic ring closing, selection for either conrotatory or disrotatory reactions modes still produces two enantiomers.
The Petasis reagent is also very air stable, and is commonly used in solution with toluene or THF. The Tebbe reagent and the Petasis reagent share a similar reaction mechanism. The active olefinating reagent, Cp 2 TiCH 2 , is generated in situ upon heating.
The observed effect in these reactions is not rate acceleration (that would be on water), but an increase in enantioselectivity. In the context of organocatalysis, both concepts of on-water reactions and in-the-presence-of-water reactions were criticized in 2007 as not so environmentally friendly by Donna Blackmond. According to Blackmond ...