Dipole moment methanol

Mercaptoethanol reagent 380 Mercury cations 144,311 Mercury lamps 20, 22 ff emission lines 23, 24 -, high pressure 22 ff -, technical data 23 Mercury(I) nitrate reagent 337 Mercury(II) salt reagent 340 Mesaconic acid 61 Mesoporphyrin 101, 102 Metal cations 310—312,398 Metal complexes 248, 398 Methanol, dipole moment 97 Methine dyestuffs 360 4-Methoxyaniline see Anisidine 4-Methoxybenzaldehyde see Anisaldehyde Methoxybenzaldehyde derivatives 72 Methoxycinnamic acid 277... 

Carbon-oxygen and carbon-halogen bonds are polar covalent bonds and carbon bears a partial positive charge in alcohols ( " C—0 ) and in alkyl halides ( " C—X ) Alcohols and alkyl halides are polar molecules The dipole moments of methanol and chloromethane are very similar to each other and to water... 

Many of the properties oj -hydroxypyridines are typical of phenols. It was long assumed that they existed exclusively in the hydroxy form, and early physical measurements seemed to confirm this. For example, the ultraviolet spectrum of a methanolic solution of 3-hydroxypyridine is very similar to that of the 3-methoxy analog, and the value of the dipole moment of 3-hydroxypyridine obtained in dioxane indicates little, if any, zwitterion formation. However, it has now become clear that the hydroxy form is greatly predominant only in solvents of low dielectric constant. Comparison of the pK values of 3-hydroxypyridine with those of the alternative methylated forms indicated that the two tautomeric forms are of comparable stability in aqueous solution (Table II), and this was confirmed using ultraviolet spectroscopy. The ratios calculated from the ultraviolet spectral data are in good agreement with those de-... 

Electrical Conductivity in Non-aqueous Solvents. Let us now discuss the random motion of an atomic ion dissolved in methanol or ethanol. It will be seen from Table 41 that the value of the dipole moment on the OH group of these molecules differs little from that of the... 

In contrast with water, methanol, ammonia, and other substances in Table 2.1, carbon dioxide, methane, ethane, and benzene have zero dipole moments. Because of the symmetrical structures of these molecules, the individual bond polarities and lone-pair contributions exactly cancel. 

It is easy to see that, for instance, water is a more polar solvent than heptane. Water has a dipole moment, is both a proton donor and acceptor and will dissolve ionic solutes. Similarly, methanol and acetonitrile are both more polar than heptane, but it is not so easy to assign relative polarities to methanol and acetonitrile. 

Substitution of methanol by another alcohol such as propanol would not be expected to radically change selectivity because in both cases a proton donor solvent is present. However, a greater change in selectivity can be expected by using ethyl ether (proton acceptor) or methylene chloride (large dipole moment). 

Po Polarity, Xe proton acceptor, Xd proton donor, Xn dipole moment, THF tetrahydrofuran, ACN acetonitrile, MeOH methanol, ATN acetone, DMF dimethylformamide, nc cannot be calculated. 

From the theoretical viewpoint, acetonitrile is the most suitable solvent to study the correlation of retention times and log P values of analytes, since the dipole moment (2.44) is nearly equal to that of water (2.55) (Figure 4.4). The electron donor effect can therefore be eliminated, and the elution order is not changed on modification of the acetonitrile-water mixture ratio. The first choice of an eluent should therefore be an acetonitrile-water mixture for non-ionic compounds in reversed-phase liquid chromatography. Methanol, acetone, THF, or DMF can then be added to improve the resolution. 

Calculations at the 6-3IG level indicate that in the gas phase, 2//-l,2,3-triazole is more stable than 1//-1,2,3-triazole by about 4.5 kcal moC. In solution, the IH isomer becomes the more stable species because the large difference in dipole moments favors the more polar tautomer. The triazolium ion (75) is predicted to be more stable than (76) by about 13.5 kcal mol <89Mi40i-0i>. 2//-1,2,3-Triazole represents more than 99.9% of the equilibrium mixture in the gas phase. However, the ab initio calculated proton affinity of 1//-benzotriazole is 10.2 kcal mol larger than that of 2//-benzotriazole, which is consistent with ICR measurements (1-methylbenzotriazole is 10 kcal mol more basic than 2-methylbenzotriazole). Measurements of enthalpies of solution, vaporization, sublimation and solvation in water, methanol and DMSO confirm the predominance of the IH tautomer in solution <89JA7348>. The energy difference between the tautomers of 1,2,3-triazole has also been estimated at the 6-31G (MP2)//3-21G level including zero-point effects. The... 

We have no measurements of micellar size, since the translation of micelle size into the number of monomers in the micelle is not a simple task and requires assumptions not easily experimentally tested. We are hopeful of extending experimentation in this direction in future research. Table II lists dielectric constants, dipole moments and effective polarities for methanol, 1- and 2-octanol, and water at 25°C. 

Comparison of dipole moments shows only small differences in polarity. From these data, it can be reasoned that micellization in methanol is feasible. Dielectric constants and effective polarities (dipole moment/molar volume) support this premise with more divergent values. It is noted that bis(2-ethyIhexyI) sodium sulfosuccinate forms micelles readily in water and 2-octanol which have the highest and lowest dielectric constants, respectively, but micelles are formed only at low concentrations in methanol whose dielectric constant is intermediate in value. 

Table II. Dielectric Constants, Dipole Moments and Effective Polarities for Methanol, Octanols and Water at 25°C...

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