Carboxylic acid amid hydrocarbons

Adsorption TLC selection of the mobile phase is conditioned by sample and stationary-phase polarities. The following polarity scale is valid for various compound classes in NPTLC in decreasing order of K values carboxylic acids>amides>amines>alcohols>aldehydes > ketones > esthers > nitro compounds > ethers > hal-ogenated compounds > aromatics >olefins > saturated hydrocarbons > fluorocarbons. For example, retention on silica gel is controlled by the number and functional groups present in the sample and their spatial locations. Proton donor/acceptor functional groups show the greatest retention, followed by dipolar molecules, and, finally, nonpolar groups. 

Potassium amide Carboxylic acids from hydrocarbons Synthesis with addition of 1 C-Atom s. 4, 614 KNHS H -> COOH... 

Carboxylic acid amides from hydrocarbons H —CONHs... 

Amines from carboxylic acid amides with simultaneous formation of hydrocarbons from tosylates... 

The considerable strengths, but also limitations, of the empirical fitting of model potentials has been established more recently, by considering a few hundred crystal structures and heats of sublimation for hydrocarbons, oxohydrocarbons, azahydrocarbons, chlorohydrocarbons, sulfohydrocarbons, sul-fones, sulfoxides, nitro compounds, carboxylic acids, amides. 

Halomethyl deri atiYes of carboxylic acid amides are obtained by the joint reaction of formaldehyde and a hydrogen halide vith amides having the type fomiula RCOXHR in which R and R represent aliphatic and cA cioaiipliatic hydrocarbon radicals . These products haA e the. structure, RCOX R CHsX, in which X represents a halogen atom. 

Solvents can be classified into three categories according to their polarity namely, polar protic, dipolar aprotic and non-polar. Most of the common solvents fall under one of following chemical classes Aliphatic hydrocarbons, aromatic hydrocarbons, alcohols, phenols, ethers, aldehydes, ketones, carboxylic acids, esters, halogen-substituted hydrocarbons, amines, nitriles, nitro-derivatives, amides and sulfur-containing solvents (Marcus, 1998). In certain cases a mixture of two or more solvents would perform better than a single solvent. 

Formally related reactions are observed when anthracene [210] or arylole-fines [211-213] are reduced in the presence of carboxylic acid derivatives such as anhydrides, esters, amides, or nitriles. Under these conditions, mono- or diacylated compounds are obtained. It is interesting to note that the yield of acylated products largely depends on the counterion of the reduced hydrocarbon species. It is especially high when lithium is used, which is supposed to prevent hydrodimerization of the carboxylic acid by ion-pair formation. In contrast to alkylation, acylation is assumed to prefer an Sn2 mechanism. However, it is not clear if the radical anion or the dianion are the reactive species. The addition of nitriles is usually followed by hydrolysis of the resulting ketimines [211-213]. 

The compositions consist of a heat-plastified mixture of an ethylene homopolymer or copolymer, about 3 to 30 pbw of an elastomer, a stability control agent, which is a partial ester of a long chain fatty acid with a polyol, higher allyl amine, fatty acid amide or olefinically unsaturated carboxylic acid copolymer, and a hydrocarbon blowing agent having from 1 to 6 carbon atoms and a boiling point between -175 and 50C. 

Compositions and functions of typical commercial products in the 2-alkyl-l-(2-hydroxyethyl)-2-imidazolines series are given in Table 29. 2-Alkyl-l-(2-hydroxyethyl)-2-imidazolines are used in hydrocarbon and aqueous systems as antistatic agents, corrosion inhibitors, detergents, emulsifiers, softeners, and viscosity builders. They are prepared by heating the salt of a carboxylic acid with (2-hydroxyethyl)ethylenediamine at 150—160°C to form a substituted amide 1 mol water is eliminated to form the substituted imidazoline with further heating at 180—200°C. Substituted imidazolines yield three series of cationic surfactants by ethoxylation to form more hydrophilic products quatemization with benzyl chloride, dimethyl sulfate, and other alkyl halides and oxidation with hydrogen peroxide to amine oxides. 

The estimation of the aqueous solubility at rmin and at other temperatures requires data on the enthalpy and the heat capacity of the solution. These properties are themselves temperature dependent and have been systematically studied for various sets of compounds such as hydrocarbons [58,59], 1-alkanols [60], alkoxyethanols, and 1,2-dialkoxyethanes [61], carboxylic acids, amines, and N-substituted amides [62], monoesters, ethylene glycol diesters, glycerol triesters [63], and crown ethers [64], Additive schemes for the estimation of aqueous solution heat capacities have been evaluated [65,66],... 

Esters arc most commonly prepared by the reaction of a carboxylic acid and an alcohol with Lhc elimination of water. Esters are also formed by a number of other reactions utilizing acid anhydrides, acid chloride s, amides, nitriles, unsaturated hydrocarbons, ethers, aldehydes, ketones, alcohols, and esters (via ester interchange). 

The results of the infrared analysis are presented in Table VI. These results show that carboxylic acids and phenols are found only in the acid concentrates. Carboxylic acids are concentrated in the polar acid subfractions III and IV while phenols are concentrated in subfraction II. Carbazoles, ketones, and amides are found in all three major nonhydrocarbon fractions. The appearance of the same compound type in several fractions may arise from differences in acidity or basicity that are caused by the hydrocarbon portion of the molecule. Multifunctionality could also be a factor in the distribution of compound types among the fractions. The 1695 cm"1 band was assigned to ketones on the basis of work... 

Saturated hydrocarbons < olefins < aromatic hydrocarbons = organic halides < sulfides < ethers < nitro compounds < esters = aldehydes = ketones < alcohols = amines < sulfones < amides < carboxylic acids... 

There are non-systematic number roots for hydrocarbon derivatives containing acyl groups or derived from acyl groups. These are the ketones, carboxylic acids, esters, nitriles, and amides ... 

Previous analysis of Uinta Basin bitumens (6,10) have shown that the predominant nitrogen types are pyrollic, amide, and aromatic nitrogen. Predominant sulfur types are sulfide, sulfoxide, and thiophenic sulfur predominant oxygen types are ketones, phenols, carboxylic acids, and possibly appreciable concentrations of furans. The aromatic (basic) nitrogen is expected to participate in irreversible adsorption on acidcracking catalysts (13) and it could require an increased cat-to-oil ratio. Previous analyses (10) have indicated also that Uinta Basin bitumen is high in naphthenic hydrocarbon and low in free paraffins. This is illustrated by the results given in Table II in which over 60% of the saturates... 

As mentioned above, the bis-amides 9a are used as precursors in the synthesis of Af-acylenamines. The conditions used for this reaction depend on the purpose of the synthesis and are described in numerous works, and reviewed in a series of articles35-37. The acid catalyst is usually concentrated sulfuric acid, but a successful application of 85% phosphoric, chlorosulfonic, methanesulfonic and formic acids was reported, and reactions were also conducted in the presence of anhydrous hydrogen chloride35. The solvents used are usually glacial acetic acid and chlorinated hydrocarbons. It is believed that the water necessary for the formation of the bis-amides under anhydrous conditions is obtained from conversion of the carboxylic acid to the anhydride, or even the sulfuric acid35. 

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