The ethyl ether, also known as diethyl ether, it is an organic compound whose chemical formula is C4H10O. It is characterized by being a colorless and volatile liquid, and therefore, its bottles should be kept closed as tightly as possible.
This ether is classified as a member of the dialkyl ethers; that is, they have the formula ROR ', where R and R' represent different carbon segments. And as described by its second name, diethyl ether, it is two -ethyl radicals that bind to the oxygen atom..
Ethyl ether was initially used as a general anesthetic, introduced in 1846 by William Thomas Green Morton. However, due to its flammability, its use was discarded, replacing it with other less dangerous anesthetics..
This compound has also been used to estimate the time of blood circulation, during the evaluation of the cardiovascular status of patients..
Within the body, diethyl ether can be transformed into carbon dioxide and metabolites; the latter end up being excreted in the urine. However, most of the administered ether is exhaled into the lungs, without undergoing any modification..
On the other hand, it is used as a solvent for soaps, oils, perfumes, alkaloids and gums..
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In the image above, there is a representation with a model of spheres and bars of the molecular structure of ethyl ether..
As can be seen, the red sphere, corresponding to the oxygen atom, has two ethyl groups linked on both sides. All the links are simple, flexible, and freely rotating around the σ axes.
These rotations give rise to stereoisomers known as conformers; that more than isomers, they are alternative spatial states. The structure of the image corresponds exactly to the anti conformer, in which all its groups of atoms are staggered (separated from each other).
What would the other conformer be? The eclipsed one, and although its image is not available, it is enough to visualize it in the shape of a U. At the upper ends of the U, the methyl groups would be located, -CH3, which would experience steric repulsions (collide in space).
Therefore, it is expected that the CH molecule3CHtwoOCHtwoCH3 adopt anti shaping most of the time.
By what intermolecular forces are the ethyl ether molecules in the liquid phase governed? They are kept in the liquid mainly thanks to dispersion forces, since their dipole moment (1.5D) lacks a sufficiently deficient region in electron density (δ +)
This is because no carbon atom in the ethyl groups gives up too much electron density to the oxygen atom. The aforementioned is evident with the electrostatic potential map of ethyl ether at hand (lower image). Note the absence of a blue region.
Oxygen cannot form hydrogen bonds either, again, because there are no O-H bonds available in the molecular structure. Therefore, it is the instantaneous dipoles and their molecular mass that favor their dispersion forces..
Despite this, it is highly soluble in water. Why? Because its oxygen atom, with a higher electron density, can accept hydrogen bonds from a water molecule:
(CH3CHtwo)twoORδ- - δ+H-OH
These interactions are responsible for 6.04g of this ether dissolving in 100mL of water.
-Diethyl ether
-Ethoxyethane
-Ethyl oxide
C4H10O or (CtwoH5)twoOR.
74.14 g / mol.
Colorless liquid.
Sweet and spicy.
Burning and sweet.
94.3 ºF (34.6 ºC) at 760 mmHg.
-177.3 ° F (-116.3 ° C). Stable crystals.
-49ºF (closed container).
6.04 g / 100mL at 25 ºC.
Miscible with short chain aliphatic alcohols, benzene, chloroform, petroleum ether, fat solvent, many oils and concentrated hydrochloric acid.
Soluble in acetone and very soluble in ethanol. It is also soluble in naphtha, benzene and oils.
0.714 mg / mL at 68 ªF (20 ºC).
2.55 (in relation to air taken with density 1).
442 mmHg at 68ºF. 538 mmHg at 25 ° C. 58.6 kPa at 20 ºC.
It is slowly oxidized by the action of air, moisture and light with the formation of peroxides.
Peroxide formation can occur in ether containers that have been opened and that remain in storage for more than six months. Peroxides can be detonated by friction, impact, or heating.
Avoid contact with: zinc, halogens, non-metallic oxyhalides, strong oxidizing agents, chromyl chloride, tementine oils, metal nitrates and chlorides.
356 ºF (180 ºC).
When heated it decomposes, emitting acrid and irritating smoke.
0.2448 cPoise at 20 ºC.
8.807 Kcal / g.
89.8 cal / g at 30 ºC.
17.06 dynes / cm at 20º C.
9.53 eV.
0.83 ppm (purity is not given).
1,355 at 15 ºC.
Ethyl ether can be obtained from ethyl alcohol, in the presence of sulfuric acid as a catalyst. Sulfuric acid in an aqueous medium dissociates producing the hydronium ion, H3OR+.
The anhydrous ethyl alcohol flows through the sulfuric acid solution, heated between 130ºC and 140ºC, producing the protonation of ethyl alcohol molecules. Subsequently, another non-protonated ethyl alcohol molecule reacts with the protonated molecule.
When this happens, the nucleophilic attack of the second ethyl alcohol molecule promotes the release of water from the first molecule (the protonated one); as a result, a protonated ethyl ether (CH3CHtwoOHCHtwoCH3), with partially positive charged oxygen.
However, this synthesis method loses efficiency because the sulfuric acid is gradually diluted with the water produced in the process (product of the dehydration of ethyl alcohol)..
The reaction temperature is critical. At temperatures below 130ºC, the reaction is slow and ethyl alcohol will be distilled for the most part..
Above 150 ºC, sulfuric acid causes the formation of ethylene (the double bond alkene), instead of combining with ethyl alcohol to form ethyl ether.
In the reverse process, that is, the hydration of ethylene in the vapor phase, ethyl ether can be formed as a by-product in addition to ethyl alcohol. In fact, this synthetic route produces most of this organic compound..
This process uses phosphoric acid catalysts attached to a solid support, which can be adjusted to produce more ether..
Vapor phase dehydration of ethanol in the presence of alumina catalysts can give a 95% yield in the production of ethyl ether..
May cause skin and eye irritation by contact. Contact with the skin can cause drying and cracking. Ether does not usually penetrate the skin, as it is quickly evaporated.
Eye irritation caused by ether is usually mild, and in the case of severe irritation, the damage is generally reversible.
Its ingestion produces narcotic effects and stomach irritation. Severe ingestion can cause kidney damage.
Inhalation of ether can cause nose and throat irritation. In the case of inhalation of ether, the following may occur: drowsiness, excitement, dizziness, vomiting, irregular breathing and increased salivation..
High exposure can cause loss of consciousness and even death.
OSHA sets an airborne occupational exposure limit of 800 ppm averaged over an 8-hour shift.
Eye irritation levels: 100 ppm (human). Eye irritation levels: 1200 mg / m3 (400 ppm).
It is an organic solvent that is used to dissolve bromine, iodine and other halogens; most lipids (fats), resins, pure rubbers, some alkaloids, gums, perfumes, cellulose acetate, cellulose nitrate, hydrocarbons and colorants.
In addition, it is used in the extraction of active principles from animal and plant tissues, because it has a lower density than water and floats on it, leaving the desired substances dissolved in the ether..
It has been used as a general anesthetic since 1840, replacing chloroform as it has a therapeutic advantage. However, it is a flammable substance, and therefore encounters severe difficulties in its use within clinical settings..
In addition, it produces some undesirable postoperative side effects such as nausea and vomiting in patients..
For these reasons, the use of ether as a general anesthetic has been discarded, replacing it with other anesthetics such as halothane..
Ether mixed with ethanol was used to form the solution called spirit of ether, used in the treatment of gastric flatulence and milder forms of gastralgia..
Ether has been used to evaluate blood circulation between an arm and the lungs. Ether is injected into an arm, bringing the blood to the right atrium, then the right ventricle, and from there to the lungs..
The time that elapses from the injection of the ether to the capture of the odor of the ether in the exhaled air is approximately 4 to 6 s.
Ether is used in teaching laboratories in many experiments; for example, in the demonstration of Mendel's laws of genetics.
Ether is used to lull the flies of the genus Drosophila and allow the necessary crosses between them, thus putting into evidence the laws of genetics
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