Anhydrides structure

COT is prepared by the polymerization of ethyne at moderate temperature and pressure in the presence of nickel salts. The molecule is non-planar and behaves as a typical cyclic olefin, having no aromatic properties. It may be catalytically hydrogenated to cyclo-octene, but with Zn and dil. sulphuric acid gives 1,3,6-cyclooclairiene. It reacts with maleic anhydride to give an adduct, m.p. 166 C, derived from the isomeric structure bicyclo-4,2,0-octa-2,4,7-triene(I) ... 

Dinitrogeri pentoxide is the anhydride of nitric acid and is prepared by removing water from pure nitric acid by means of phosphorus (V) oxide. It is a crystalline solid having the ionic structure of (N02) (N03) , nitronium nitrate (the nitronium ion is mentioned later). It decomposes above 273 K, thus ... 

Both acids 3deld succinic acid, m.p. 185°, upon catalytic reduction (see Section 111,150), thus establishing their structures. Maleic and fumaric acids are examples of compounds exhibiting cis-trans isomerism (or geometric isomerism). Maleic acid has the cm structure since inter alia it readily 3delds the anhydride (compare Section 111,93). Fumaric acid possesses the trans structure it does not form an anhydride, but when heated to a high temperature gives maleic anhydride. 

It may be pointed out that dehydration of p hydroxy esters with fused potassium hydrogen sulphate, acetic anhydride, phosphoric oxide or with tliionyl chloride in benzeue solution leads to ap unsiiturated esters containing some PY-unsaturated ester the proportion of the latter depends not only upon the structure of the ester but also upon the dehydrating agent used. Elehydration occasionally occurs during the reaction itself or upon attempted distillation. 

By controlhng the relative amounts of, for example, glycerol and phthahc anhydride and the experimental conditions of the reaction, various pol5 mers of different properties are obtained. Under mild conditions (ca. 150°) only the primary alcohol groups are esterified and the secondary alcohol group remains free. The structural unit of the resulting linear polymer is ... 

Davies and Warren" found that when 1,4-dimethylnaphthalene was treated with nitric acid in acetic anhydride, and the mixture was quenched after 34 hr, a pale yellow solid with an ultraviolet spectrum similar to that of a-nitro-naphthalene was produced. However, if the mixture was allowed to stand for 5 days, the product was i-methyl-4 nitromethylnaphthalene, in agreement with earlier findings. Davies and Warren suggested that the intermediate was 1,4-dimethyl-5 nitronaphthalene, which underwent acid catalysed rearrangement to the final product. Robinson pointed out that this is improbable, and suggested an alternative structure (iv) for the intermediate, together with a scheme for its formation from an adduct (ill) (analogous to l above) and its subsequent decomposition to the observed product. 

The preparation of these [4-hydroxy-THISs, (1), X = O] by cydization of a-carboxy-N-arylthiobenzimides (5) by treatment with acetic anhydride and triethylamine has been investigated in detail, and the structure has been revised for the compound previously described as 2.3-diphenyl-4-hydroxythiazolium hydroxide inner salt (1, X = 0, R = R = Ph, R = H) (Scheme 5) (3, 10). 4-Hydroxy-THlSs also arise by condensation of gem-dicyanoepoxides with thioamides (Scheme 6) (8). 

Furthermore, if the structural unit to be polymerized is a vinyl group, mixed reactions can be carried out with a second compound such as a vinyl derivative or maleic anhydride. 

Succinic anhydride the structure of which is shown is a cyclic... 

Figure 20 1 shows the structures of various derivatives of acetic acid (acetyl chlo ride acetic anhydride ethyl thioacetate ethyl acetate and acetamide) arranged m order... 

Step 2 Structurally O acylisoureas resemble carboxylic acid anhydrides and are powerful acylatmg agents In the reaction s second stage the amine adds to the carbonyl group of the O acylisourea to give a tetrahedral intermediate... 

Poly(amide-imide) is the condensation polymer of 1,2,4-benzenetricarboxylic anhydride and various aromatic diamines and has the general structure ... 

Write structural formulas for maleic anhydride (M ) and stilbene (M2). Neither of these monomers homopolymerize to any significant extent, presumably owing to steric effects. These monomers form a copolymer,... 

Properties and Structure. Phosphoms(V) oxide, the extremely hygroscopic acid anhydride of the phosphoric acids, exists in several forms but is often referred to by its empirical formula, P2O3. Three crystalline polymorphs, two distinct Hquids, and several amorphous or glassy soHds are recogni2ed. Some properties of the various forms of phosphoric oxide are Hsted in Table 10. 

Table 2. Structure and Properties of Aromatic Diamines and Acid Anhydrides Used in Epoxy-Matrix Resins...

The Diels-Alder addition of maleic anhydride gave a compound for which two structures were proposed (Scheme 41) (66DIS(B)102,43JCS654). 

By virtue of their fused /3-lactam-thiazolidine ring structure, the penicillins behave as acylating agents of a reactivity comparable to carboxylic acid anhydrides (see Section 5.11.2.1). This reactivity is responsible for many of the properties of the penicillins, e.g. difficult isolation due to hydrolytic instability (B-49MI51102), antibacterial activity due to irreversible transpeptidase inhibition (Section 5.11.5.1), and antigen formation via reaction with protein molecules. 

Styryl sulfonyl chloride Friedel-Crafts cyclization benzo[h]thiophenes from, 4, 873 Succinic anhydrides polymers, I, 277 mass spectrometry, 4, 585 structure, 4, 552... 

Systems based on isophthalic acid often show better water and alkali resistance than those based on phthalic anhydride. This is not thought to be due to inherent differences between the phthalic and isophthalic structures but is ascribed to the fact that isophthalate resins have generally considerably higher viscosities which enable them to be diluted with greater amounts of styrene. It is the additional proportion of styrene which gives the improved water and alkali resistance. 

The major aromatics (organics having at least one ring structure with six carbon atoms) manufactured include benzene, toluene, xylene, and naphthalene. Other aromatics manufactured include phenol, chlorobenzene, styrene, phthalic and maleic anhydride, nitrobenzene, and aniline. Benzene is generally recovered from cracker streams at petrochemical plants and is used for the manufacture of phenol, styrene, aniline, nitrobenzene, sulfonated detergents, pesticides such as hexachlorobenzene, cyclohexane (an important intermediate in synthetic fiber manufacture), and caprolactam, used in the manufacture of nylon. Benzene is also used as a general purpose solvent. 

The chemistry of carboxylic acids is the central theme of this chapter. The importance of carboxylic acids is magnified when we realize that they are the parent compounds of a large group of derivatives that includes acyl chlorides, acid anhydrides, esters, and amides. Those classes of compounds will be discussed in Chapter 20. Together, this chapter and the next tell the story of some of the most fundamental structural types and functional group transfonnations in organic and biological chemistry. 

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