Organic compounds esters

In the presence of potassium tert-butylate and as with most organic compounds, esters combust spontaneousiy after a period of induction that is generally very short. Such accidents have been reported with propyl formate, ethyl acetate and dimethyl carbonate. 

Like many organic compounds, esters can be reduced in two ways (a) by catalytic hydrogenation using molecular hydrogen, or (b) by chemical reduction. In either case, the ester is cleaved to yield (in addition to the alcohol or phenol from which it was derived) a primary alcohol corresponding to the acid portion of the ester. 

Identify the class of organic compounds (ester, ether, ketone, and so on) to which each of the following belongs. 

Sodium and potassium hydroxides. The use of these efficient reagents is generally confined to the drying of amines (soda lime, barium oxide and quicklime may also be employed) potassium hydroxide is somewhat superior to the sodium compound. Much of the water may be first removed by shaking with a concentrated solution of the alkali hydroxide. They react with many organic compounds (e.g., acids, phenols, esters and amides) in the presence of water, and are also soluble in certain organic liquids so that their use as desiccants is very limited... 

Metallic sodium is vital in the manufacture of esters and in the preparation of organic compounds. The metal may be used to improve the structure of certain alloys, to descale metal, and to purify molten metals. 

Essential oils (Section 26 7) Pleasant smelling oils of plants consisting of mixtures of terpenes esters alcohols and other volatile organic substances Ester (Sections 4 1 and 20 1) Compound of the type... 

Potassium fluoride [7789-23-3], KF, is the most frequently used of the alkaU metal fluorides, although reactivity of the alkaU fluorides is in the order CsF > RbF > KF > NaF > LiF (6). The preference for KF is based on cost and availabiUty traded off against relative reactivity. In its anhydrous form it can be used to convert alkyl haUdes and sulfonyl haUdes to the fluorides. The versatility makes it suitable for halogen exchange in various functional organic compounds like alcohols, acids and esters (7). For example, 2,2-difluoroethanol [359-13-7] can be made as shown in equation 9 and methyl difluoroacetate [433-53 ] as in equation 10. 

Nitration is defined in this article as the reaction between a nitration agent and an organic compound that results in one or more nitro (—NO2) groups becoming chemically bonded to an atom in this compound. Nitric acid is used as the nitrating agent to represent C-, 0-, and N-nitrations. O-nitrations result in esters. N-nitrations result in nitramines. 

Most organic compounds, including aromatic hydrocarbons, alcohols, esters, ketones, ethers, and carboxyUc acids are miscible with nitroparaffins, whereas alkanes and cycloalkanes have limited solubiUty. The lower nitroparaffins are excellent solvents for coating materials, waxes, resins, gums, and dyes. 

ROOC—COOH, are not. The dialkyl esters are characterized by good solvent properties and serve as starting materials in the synthesis of many organic compounds, such as pharmaceuticals, agrochemicals, and fine chemicals (qv). Among the diesters, dimethyl, diethyl, and di- -butyl oxalates are industrially important. Their physical properties are given in Table 7. 

Like the lower alcohols, amyl alcohols are completely miscible with numerous organic solvents and are excellent solvents for nitrocellulose, resia lacquers, higher esters, and various natural and synthetic gums and resius. However, iu contrast to the lower alcohols, they are only slightly soluble iu water. Only 2-methyl-2-butanol exhibits significant water solubiUty. As associated Hquids, amyl alcohols form a2eotropes with water and//or a variety of organic compounds (Table 3). 

Sulfation is defined as any process of introducing an SO group into an organic compound to produce the characteristic C—OSO configuration. Typically, sulfation of alcohols utilizes chlorosulfuric acid or sulfur trioxide reagents. Unlike the sulfonates, which show remarkable stability even after prolonged heat, sulfated products are unstable toward acid hydrolysis. Hence, alcohol sulfuric esters are immediately neutralized after sulfation in order to preserve a high sulfation yield. 

The corrosion behavior of tantalum is weU-documented (46). Technically, the excellent corrosion resistance of the metal reflects the chemical properties of the thermal oxide always present on the surface of the metal. This very adherent oxide layer makes tantalum one of the most corrosion-resistant metals to many chemicals at temperatures below 150°C. Tantalum is not attacked by most mineral acids, including aqua regia, perchloric acid, nitric acid, and concentrated sulfuric acid below 175°C. Tantalum is inert to most organic compounds organic acids, alcohols, ketones, esters, and phenols do not attack tantalum. 

For the properties of these compounds, see Esters, organic. For esters of inorganic acids, see the articles on nitric acid, phosphoric acids, sulfuric acid, etc. 

Ethers, esters, amides and imidazolidines containing an epithio group are said to be effective in enhancing the antiwear and extreme pressure peiformance of lubricants. Other uses of thiiranes are as follows fuel gas odorant (2-methylthiirane), improvement of antistatic and wetting properties of fibers and films [poly(ethyleneglycol) ethers of 2-hydroxymethyl thiirane], inhibition of alkene metathesis (2-methylthiirane), stabilizers for poly(thiirane) (halogen adducts of thiiranes), enhancement of respiration of tobacco leaves (thiirane), tobacco additives to reduce nicotine and to reduce phenol levels in smoke [2-(methoxymethyl)thiirane], stabilizers for trichloroethylene and 1,1,1-trichloroethane (2-methylthiirane, 2-hydroxymethylthiirane) and stabilizers for organic compounds (0,0-dialkyldithiophosphate esters of 2-mercaptomethylthiirane). The product of the reaction of aniline with thiirane is reported to be useful in the flotation of zinc sulfide. 

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