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Hydrogen chloride, polar

It is clear from Table 1 that, for a few highly polar molecules such as water, the Keesom effect (i.e. freely rotating permanent dipoles) dominates over either the Debye or London effects. However, even for ammonia, dispersion forces account for almost 57% of the van der Waals interactions, compared to approximately 34% arising from dipole-dipole interactions. The contribution arising from dispersion forces increases to over 86% for hydrogen chloride and rapidly goes to over 90% as the polarity of the molecules decrease. Debye forces generally make up less than about 10% of the total van der Waals interaction. [Pg.174]

Examine electrostatic potential maps for potassium hydride and hydrogen chloride. How are they similar and how are they different (Focus on whether the molecules are polar or nonpolar (compare dipole moments), and on the electronic character of hydrogen.) Draw the ionic Lewis structure that is most consistent with each electrostatic potential map. Does each atom have a filled valence shell ... [Pg.123]

A Bronsted-Lowry acid is a substance that donates a proton (H+), and a Bronsted-Lowry base is a substance that accepts a proton. (The name proton is often used as a synonym for hydrogen ion, H+, because loss of the valence electron from a neutral hydrogen atom leaves only the hydrogen nucleus— a proton.) When gaseous hydrogen chloride dissolves in water, for example, a polar HC1 molecule acts as an acid and donates a proton, while a water molecule acts as a base and accepts the proton, yielding hydronium ion (H30+) and chloride ion (Cl-). [Pg.49]

Surface modification reactions are used to improve the wettability of glass surfaces by polar stationary phases and to Improve the extent of deactivation by sllylation" [138-146,166]. Miaaiuua procedures have been investigated but only a few are in use. Of these, the most important reactions are etching by hydrogen chloride, leaching with aqueous hydrochloric acid, formation of whiskers and solution deposition of a layer of solid particles. Because of the high purity and thinness of the... [Pg.593]

Fluoride ion catalyzes the hydrosilylation of both alkyl and aryl aldehydes to silyl ethers that can be easily hydrolyzed to the free alcohols by treatment with 1 M hydrogen chloride in methanol.320 The most effective sources of fluoride are TBAF and tris(diethylamino)sulfonium difluorotrimethylsilicate (TASF). Somewhat less effective are CsF and KF. Solvent effects are marked. The reactions are facilitated in polar, aprotic solvents such as hexamethylphosphortriamide (HMPA) or 1,3-dimethyl-3,4,5,6-tetrahydro-2(l //)-pyrirnidinone (DMPU), go moderately well in dimethylformamide, but do not proceed well in either tetrahydrofuran or dichloromethane. The solvent effects are dramatically illustrated in the reaction of undecanal and dimethylphenylsilane to produce undecyloxyphenyldimethylsi-lane. After one hour at room temperature with TBAF as the source of fluoride and a 10 mol% excess of silane, yields of 91% in HMPA, 89% in DMPU, 56% in dimethylformamide, 9% in tetrahydrofuran, and only 1% in dichloromethane are obtained (Eq. 164).320... [Pg.60]

The formation of hydrogen chloride in the reaction medium can lead to products of its addition to the olefinic linkage.156 Yields of such adducts are increased by the use of solvents of low polarity that are weak electron acceptors, such as dichlorodimethylsilane (Equation 4.34).157... [Pg.129]

This enhanced reactivity of fluoromethyl cyanide is undoubtedly due to the inductive effect of the fluorine atom which produces an electron deficit on the carbon atom linked to the nitrogen, and presumably increases still further the polarity of the carbon-nitrogen bond, so that the electron displacements can be pictured as (IX). The increased polarity of the carbon-nitrogen bond will obviously facilitate polar addition of hydrogen chloride and alcohols (or phenols). [Pg.141]

Formula HCl MW 36.461 a polar molecule, dipole moment 1.12D H—Cl bond energy 105.5 kcal/mol internuclear distance 1.28A. Hydrochloric acid is an aqueous solution of hydrogen chloride. [Pg.357]

During the dark, polar winter the temperature drops to extremely low values, on the order of-80°C. At these temperatures, water and nitric acid form polar stratospheric clouds. Polar stratospheric clouds are important because chemical reactions in the stratosphere are catalyzed on the surface of the crystals forming these clouds. The chemical primarily responsible for ozone depletion is chlorine. Most of the chlorine in the stratosphere is contained in the compounds hydrogen chloride, HCl, or chlorine nitrate, CIONO. Hydrogen chloride and chlorine nitrate undergo a number of reactions on the surface of the crystals of polar stratospheric clouds. Two important reactions are ... [Pg.264]

Addition Reactions. In general, polar molecules such as hydrogen halides add across the B—N bonds, the more electronegative group bonding to boron (91). The adducts are cydotriborazanes such as the product formed by reaction of B-trichloroborazine and hydrogen chloride (eq. 35). X-ray crystal analysis shows the structure exists in a chair conformation (124). [Pg.266]

From the concepts discussed in Chapter 6, you should be able to deduce that hydrogen chloride is a somewhat polar molecule. This gaseous material, therefore, has a good solubility in water by virtue of the dipole-dipole attractions occurring between the HC1 and H20 molecules. [Pg.689]

Methylpropene reacts with ethene and hydrogen chloride under polar conditions to yield 1-chloro-3,3-dimethylbutane. Show a mechanism for this reaction that is consistent with the reactants, conditions, and product. Give your reasoning. [Pg.401]

Also called dipolar attraction, this is the attraction between the opposite (partial) charges of polar molecules. Obviously, dipolar attractions occur only between polar molecules. A dipole-dipole attraction is shown below for a pair of hydrogen chloride molecules. The dipole-dipole attractive force is indicated with a blue dashed line. [Pg.166]


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