Of ethane

The reaction between hydrogen and chlorine is probably also of this type and many organic free radical reactions (e.g. the decomposition of ethanal) proceed via chain mechanisms. 

CCls CHO. A colourless oily liquid with a pungent odour b.p. 98°C. Manut actured by the action of chlorine on ethanol it is also made by the chlorination of ethanal. When allowed to stand, it changes slowly to a white solid. Addition compounds are formed with water see chloral hydrate), ammonia, sodium hydrogen sulphite, alcohols, and some amines and amides. Oxidized by nitric acid to tri-chloroethanoic acid. Decomposed by alkalis to chloroform and a methanoate a convenient method of obtaining pure CHCI3. It is used for the manufacture of DDT. It is also used as a hypnotic. 

Manufactured by the liquid-phase oxidation of ethanal at 60 C by oxygen or air under pressure in the presence of manganese(ii) ethanoate, the latter preventing the formation of perelhanoic acid. Another important route is the liquid-phase oxidation of butane by air at 50 atm. and 150-250 C in the presence of a metal ethanoate. Some ethanoic acid is produced by the catalytic oxidation of ethanol. Fermentation processes are used only for the production of vinegar. 

CH2 CH CH0. a colourless, volatile liquid, with characteristic odour. The vapour is poisonous, and intensely irritating to eyes and nose b.p. 53"C. It is prepared by the distillation of a mixture of glycerin, potassium sulphate and potassium hydrogen sulphate. It is manufactured by direct oxidation of propene or cross-condensation of ethanal with meth-anal. 

The hydrocarbons are separated in another column and analyzed by a flame ionization detector, FID. As an example, Figure 3.13 shows the separation obtained for a propane analyzed according to the ISO 7941 standard. Note that certain separations are incomplete as in the case of ethane-ethylene. A better separation could be obtained using an alumina capillary column, for instance. 

Once the bubble point is reached (at point B), the first bubble of ethane vapour is released. From point B to C liquid and gas co-exist in the cell, and the pressure is maintained constant as more of the liquid changes to the gaseous state. The system exhibits infinite compressibility until the last drop of liquid is left In the cell (point C), which is the dew point. Below the dew point pressure only gas remains in the cell, and as pressure is reduced below the dew point, the volume increase is determined by the compressibility of the gas. The gas compressibility is much greater than the liquid compressibility, and hence the change of volume for a given reduction in pressure (the... 

If the experiment was now reversed, starling from A and increasing the pressure, the first drop of ethane liquid would appear at point C, the dew point of the gas. Remember that throughoufthis process, isothermal conditions are maintained. 

Figure 5.20 Pressure-temperature phase diagram mixture of ethane and n-heptane...

Moving back to the overall picture, it can be seen that as the fraction of ethane in the mixture changes, so the position of the two-phase region and the critical point change, moving to the left as the fraction of the lighter component (ethane) increases. 

Sales gas, which is typically made up of methane (CH ) and small amounts of ethane (C2Hg), can be exported by refrigerated tanker rather than by pipeline and has to be compressed by a factor of 600 (and cooled to -150°C). This is then termed Liquefied Natural Gas (LNG). 

One can effectively reduce the tliree components to two with quasibinary mixtures in which the second component is a mixture of very similar higher hydrocarbons. Figure A2.5.31 shows a phase diagram [40] calculated from a generalized van der Waals equation for mixtures of ethane n = 2) with nomial hydrocarbons of different carbon number n.2 (treated as continuous). It is evident that, for some values of the parameter n, those to the left of the tricritical point at = 16.48, all that will be observed with increasing... 

Figure A2.5.31. Calculated TIT, 0 2 phase diagram in the vicmity of the tricritical point for binary mixtures of ethane n = 2) witii a higher hydrocarbon of contmuous n. The system is in a sealed tube at fixed tricritical density and composition. The tricritical point is at the confluence of the four lines. Because of the fixing of the density and the composition, the system does not pass tiirough critical end points if the critical end-point lines were shown, the three-phase region would be larger. An experiment increasing the temperature in a closed tube would be represented by a vertical line on this diagram. Reproduced from [40], figure 8, by pennission of the American Institute of Physics.

Figure A3.10.20 Arrhenius plot of ethane hydrogenolysis aetivity for Ni(lOO) and Ni(l 11) at 100 Torr and H2/C2Hg = 100. Also ineluded is the hydrogenolysis aetivity on supported Ni eatalysts at 175 Torr and H2/C2H6 = 6.6 [43].

Engstrom J R, Goodman D W and Weinberg W H 1988 Hydrogenolysis of ethane, propane, n-butane and neopentane... 

Burcat A, Skinner G B, Crossley R W and Scheller K 1973 High temperature decomposition of ethane Int. J. Chem. Kinetics 5 345-52... 

The reaction usually proceeds with explosive violence and a better method of preparation is to heat, gently, moist crystals of ethane-dioic acid (oxalic acid) and potassium chlorate(V) ... 

Mercury compounds (for example mercury(II) chloride) are used in medicine because of their antiseptic character. The artificial red mercury(Il) sulphide is the artist s vermilion . Mercury(II) sulphate is a catalyst in the manufacture of ethanal from ethyne ... 

Figure 2-15, Distance matrices of ethanal with a) geometric distances in A and b) topological distances. The matrix elements of b) result from counting the number of bonds along the shortest walk between the chosen atoms,...

Figure 2-16. a) The redundant incidence matrix of ethanal can be compressed by b) omitting the zero values and c) omitting the hydrogen atoms, in the non-square matrix, the atoms are listed in columns and the bonds in rows. 

Figure 2-17. a) The redundanl bond malrix of ethanal with ihe zero values omitted, b) It can be compressed by reduction to the top right triangle, c) Omitting the hydrogen atoms provides the simplest non-redundant matrix representation. 

Figure 2-19. The BE-matriK of ethanal allows one to determine tine number of valence electrons (the sum of each row) on the atoms and to validate the octet rule,...

Figure 2-20. A connection table the structure diagram of ethanal, with the atoms arbitrarily labeled, is defined by a list of atoms and a list of bonds.

Figure 2-22. Non-redundant connection table of ethanal. Only non-hydrogen atoms are considered bonds with the lowest indices are counted once (see Figure 2-21).

The origin of a torsional barrier can be studied best in simple cases like ethane. Here, rotation about the central carbon-carbon bond results in three staggered and three eclipsed stationary points on the potential energy surface, at least when symmetry considerations are not taken into account. Quantum mechanically, the barrier of rotation is explained by anti-bonding interactions between the hydrogens attached to different carbon atoms. These interactions are small when the conformation of ethane is staggered, and reach a maximum value when the molecule approaches an eclipsed geometry. 

Schematic illustration of the arrangements of ethane molecules in slits of varying sizes. In the slit of width ochJ tich methyl group is able to occupy a potential minimum from the pore (middle). 

Using the heat parameters from Problem 12, calculate of ethane. The... 

In the case of ethylene, because of 2-fold symmetry, odd terms drop out of the series, V3, V5,... = 0. In the case of ethane, because of 3-fold symmeti-y, even temis drop out, V2, V4,... = 0. Terms higher than three, even though permitted by symmetry, are usually quite small and force fields can often be limited to three torsional terms. Like cubic and quaitic terms modifying the basic quadratic approximation for stretching and bending, terms in the Fourier expansion of Ftors (to) beyond n = 3 have limited use in special cases, for example, in problems involving octahedrally bound complexes. In most cases we are left with the simple expression... 

Add 4 0 g. (4 0 ml.) of pure anihne dropwise to a cold solution of ethyl magnesium bromide (or iodide) prepared from 1 Og. of magnesium, 5 0 g. (3-5 ml.) of ethyl bromide (or the equivalent quantity of ethyl iodide), and 30 ml. of pure, sodium-dried ether. When the vigorous evolution of ethane has ceased, introduce 0 02 mol of the ester in 10 ml. of anhydrous ether, and warm the mixture on a water bath for 10 minutes cool. Add dilute hydrochloric acid to dissolve the magnesium compounds and excess of aniline. Separate the ethereal layer, dry it with anhydrous magnesium sulphate and evaporate the ether. Recrystallise the residual anihde, which is obtained in almost quantitative yield, from dilute alcohol or other suitable solvent. 

---