Radicals formulae

The first column (Substance) in each table describes the structure of the radical species, arranged in ascending order of the empirical formula. Radicals with related structures have been collected in groups. 

Radical formula Radical properties A,G, "of sulfur parent... 

Of the general formula, R - S — H, where R represents an aliphatic or cyclic radical, the thiols —also known as mercaptans— are acidic in behavior owing to their S—H functional group they are corrosive and malodorous. Their concentration in crude oils is very low if not zero, but they are created from other sulfur compounds during refining operations and show up in the light cuts, as illustrated in Table 8.6. 

Benzoyl peroxide is a com monly used free radical ini tiator It has the formula O O... 

TABLE 1.13 Names and Formulas of Organic Radicals Continued)... 

Free Radicals. In the formula of a polyatomic radical an unpaired electron(s) is(are) indicated by a dot placed as a right superscript to the parentheses (or square bracket for coordination compounds). In radical ions the dot precedes the charge. In structural formulas, the dot may be placed to indicate the location of the unpaired electron(s). 

Abbreviations for Ligand Names. Except for certain hydrocarbon radicals, for ligand (L) and metal (M), and a few with H, all abbreviations are in lowercase letters and do not involve hyphens. In formulas, the ligand abbreviation is set off with parentheses. Some common abbrevia-... 

Hydroxy-2-methylpropanenitrile is then reacted with methanol (or other alcohol) to yield methacrylate ester. Free-radical polymerization is initiated by peroxide or azo catalysts and produce poly(methyl methacrylate) resins having the following formula ... 

Poly (methyl Acrylate). The monomer used for preparing poly(methyl acrylate) is produced by the oxidation of propylene. The resin is made by free-radical polymerization initiated by peroxide or azo catalysts and has the following formula ... 

Alkylation of cyclohexane with isoprene can be carried out with alkyl radicals formed at 450°C and 20.3 MPa (200 atm) (73). 40% Pentenylcyclohexanes, 20% dipentenes (ie, substances having the general formula C qH ), and 40% higher boiling compounds are obtained using a 6.8 molar ratio of cyclohexane to isoprene and a space velocity of 2.5. Of the pentenylcyclohexanes, the head and tail products are in equal amounts. Even... 

During Stages II and III the average concentration of radicals within the particle determines the rate of polymerization. To solve for n, the fate of a given radical was balanced across the possible adsorption, desorption, and termination events. Initially a solution was provided for three physically limiting cases. Subsequentiy, n was solved for expHcitiy without limitation using a generating function to solve the Smith-Ewart recursion formula (29). This analysis for the case of very slow rates of radical desorption was improved on (30), and later radical readsorption was accounted for and the Smith-Ewart recursion formula solved via the method of continuous fractions (31). 

Nloha.tes, Niobic acid is amphoteric and can act as an acid radical in several series of compounds, which are referred to as niobates. Niobic acid is soluble in solutions of the hydroxides of alkaH metals to form niobates. Fusion of the anhydrous pentoxide with alkaH metal hydroxides or carbonates also yields niobates. Most niobates are insoluble in water with the exception of those alkaH metal niobates having a base-to-acid ratio greater than one. The most weU-known water-soluble niobates are the 4 3 ad the 7 6 salts (base acid), having empirical formulas MgNb O c, (aq) and M24Nb2202y (aq), respectively. The hexaniobate is hydrolyzed in aqueous solution according to the pH-dependent reversible equiHbria (130), when the pH is ca 9. 

Polyethylene (PE) is a genetic name for a large family of semicrystalline polymers used mostiy as commodity plastics. PE resins are linear polymers with ethylene molecules as the main building block they are produced either in radical polymerization reactions at high pressures or in catalytic polymerization reactions. Most PE molecules contain branches in thek chains. In very general terms, PE stmcture can be represented by the following formula ... 

Dialkyl peroxides have the stmctural formula R—OO—R/ where R and R are the same or different primary, secondary, or tertiary alkyl, cycloalkyl, and aralkyl hydrocarbon or hetero-substituted hydrocarbon radicals. Organomineral peroxides have the formulas R Q(OOR) and R QOOQR, where at least one of the peroxygens is bonded directly to the organo-substituted metal or metalloid, Q. Dialkyl peroxides include cyclic and bicycflc peroxides where the R and R groups are linked, eg, endoperoxides and derivatives of 1,2-dioxane. Also included are polymeric peroxides, which usually are called poly(alkylene peroxides) or alkylene—oxygen copolymers, and poly(organomineral peroxides) (44), where Q = As or Sb. 

Carbonates are indexed in Chemicaly hstracts under carbonic acid, esters. Symmetrical diesters have the prefix di or bis. Unsymmetrical diesters are listed with the two radicals following each other. For example, ethyl phenyl carbonic diester is C2H OCOOC H. Table 6 Hsts commonly used carbonates, their Chemicaly hstracts Service Registry Number, and formulas. 

It resembles tetracyanoethylene in that it adds reagents such as hydrogen (31), sulfurous acid (31), and tetrahydrofuran (32) to the ends of the conjugated system of carbon atoms suffers displacement of one or two cyano groups by nucleophilic reagents such as amines (33) or sodiomalononittile (34) forms TT-complexes with aromatic compounds (35) and takes an electron from iodide ion, copper, or tertiary amines to form an anion radical (35,36). The anion radical has been isolated as salts of the formula (TCNQ) where is a metal or ammonium cation, and n = 1, 1.5, or 2. Some of these salts have... 

Trigonometric Substitution This technique is particularly well adapted to integrands in the form of radicals. For these the function is transformed into a trigonometric form. In the latter form they may be more easily recognizable relative to the identity formulas. These functions and their transformations are... 

Naphthenic acid is a collective name for organic acids present in some but not all crude oils. In addition to true naphthenic acids (naphthenic carboxylic acids represented by the formula X-COOH in which X is a cycloparaffin radical), the total acidity of a crude may include various amounts of other organic acids and sometimes mineral acids. Thus the total neutralization number of a stock, which is a measure of its total acidity, includes (but does not necessaiily represent) the level of naphthenic acids present. The neutralization number is the number of milligrams of potassium hydroxide required to neutralize one gram of stock as determined by titration using phenolphthalein as an indicator, or as determined by potentiometric titration. It may be as high as 10 mg KOH/gr. for some crudes. The neutralization number does not usually become important as a corrosion factor, however, unless it is at least 0.5 mg KOH/gm. 

The compounds formed when a hydroxyl group (-OH) is substituted for a hydrogen are called alcohols. They have the general formula R-OH. The hydroxyl radical looks exactly like the hydroxide ion, but it is not an ion. Where the hydroxide ion fits the definition of a complex ion - a chemical combination of two or more atoms that have colleetively lost or (as in this case) gained one or more electrons - the... 

The substitution of one hydroxyl radical for a hydrogen atom in propane produces propyl alcohol, or propanol, which has several uses. Its molecular formula is C3H7OH. Propyl alcohol has a flash point of 77°F and, like all the alcohols, bums with a pale blue flame. More commonly known is the isomer of propyl alcohol, isopropyl alcohol. Since it is an isomer, it has the same molecular formula as propyl alcohol but a different structural formula. Isopropyl alcohol has a flash point of 53 F. Its ignition temperamre is 850°F, while propyl alcohol s ignition temperature is 700 F, another effect of the different stmcture. Isopropyl alcohol, or 2-propanol (its proper name) is used in the manufacture of many different chemicals, but is best known as rubbing alcohol. 

Whenever a hydrocarbon backbone has two hydroxyl radicals attached to it, it becomes a special type of alcohol known as a glycol. The simplest of the glycols, and the most important, is ethylene glycol, whose molecular formula C2H4(OH)2. The molecular formula can also be written CHjOHCHjOH and may be printed as such on some labels. Ethylene glycol is a colorless, thick liquid with a sweet taste, is toxic by ingestion and by inhalation, and among its many uses is a permanent antifreeze and coolant for automobiles. It is a combustible liquid with a flash point of 240"F. 

The last group of substituted hydrocarbons produced by adding hydroxyl radicals to the hydrocarbon backbone are the compounds made when three hydroxyl radicals are substituted these are known as glycerols. The name of the simplest of this type of compound is just glycerol. Its molecular formula is 3115(011)3. Glycerol is a colorless, thick, syrupy liquid with a sweet taste, and has a flash point of 320°F, and is used to make such diverse products as candy and explosives, plus many more. Other glycerols are made, but most of them are not classified as hazardous materials. 

The simplest of the ethers would be ether that has the simplest hydrocarbon backbones attached those backbones are the radicals of the simplest hydrocarbon, methane. Therefore, the simplest of the ethers is dimethyl ether, whose formula is CH3OCH3. Dimethyl is used because there are two methyl radicals, and di-" is the prefix for two. This compound could also be called methyl methyl ether, or just... 

The ketones are a group of compounds with the general formula R-C-R. The -C-functional group is known as the carbonyl group or carbonyl radical it appears in many different classes of hydrocarbon derivatives. There are only a few important ketones, and they are all extremely hazardous. 

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