Saturated/unsaturated compounds

Hydrotreatment Catalytic process used to saturate unsaturated compounds in crude oil products or to remove heteroatoms from crude oil fractions. Process carried out under a hydrogen atmosphere. 

The double bond is not stronger than the single bond on the contrary, it is more vulnerable, making unsaturated compounds more chemically reactive than the saturates. 

The principal direct appHcation of furfural is as a selective solvent. It is used for separating saturated from unsaturated compounds in petroleum refining, for the extractive distillation of butadiene and other hydrocarbons in the manufacture of synthetic mbber and for the production of... 

Aqueous mineral acids react with BF to yield the hydrates of BF or the hydroxyfluoroboric acids, fluoroboric acid, or boric acid. Solution in aqueous alkali gives the soluble salts of the hydroxyfluoroboric acids, fluoroboric acids, or boric acid. Boron trifluoride, slightly soluble in many organic solvents including saturated hydrocarbons (qv), halogenated hydrocarbons, and aromatic compounds, easily polymerizes unsaturated compounds such as butylenes (qv), styrene (qv), or vinyl esters, as well as easily cleaved cycHc molecules such as tetrahydrofuran (see Furan derivatives). Other molecules containing electron-donating atoms such as O, S, N, P, etc, eg, alcohols, acids, amines, phosphines, and ethers, may dissolve BF to produce soluble adducts. 

Carbocyclic compounds are very usefully divided into (a) saturated (alicyclic) compounds, (b) aromatic compounds and (c) the intermediate partially unsaturated (alicyclic) compounds. Heterocyclic compounds can be subdivided in exactly the same way, and equally usefully. 

Unsaturated alcohols may be converted to saturated carbonyl compounds as a result of migration (75). When migration relative to saturation is high, the isomerization gains synthetic utility (9,49). 

Products from coking processes vary considerably with feed type and process conditions. These products are hydrocarbon gases, cracked naphtha, middle distillates, and coke. The gas and liquid products are characterized by a high percentage of unsaturation. Hydrotreatment is usually required to saturate olefinic compounds and to desulfurize products from coking units. 

Catalytic systems at very low metal loading 0.1% (w/w) obtained in this way can be conveniently used in the hydrogenation of a,P-unsaturated ketones to the corresponding saturated carbonyl compounds with very high efficiencies and selectivities. In Table 4 we report the results obtained in the selective hydrogenation of 4-(6-methoxy-2-naphthyl)-3-buten-2-one, 1, and 2-acetyl-5,8-dimethoxy-3,4-dihydronaphthalene, 2, to the corresponding saturated carbonyl products (I), which are important intermediates... 

The nature of dangerous reactions involving organic chemicals depends on the saturated, unsaturated or aromatic structures of a particular compound. Saturated hydrocarbons are hardly reactive, especially when they are linear. Branched or cyclic hydrocarbons (especially polycyclic condensed ones) are more reactive, in particular as with oxidation reactions. With ethylenic or acetylenic unsaturated compounds, the products are endothermic . 

Another general process involves the reaction of Pd(0) species with halides or sulfonates by oxidative addition, generating reactive intermediates having the organic group attached to Pd(II) by a ct bond. The oxidative addition reaction is very useful for aryl and alkenyl halides, but the products from saturated alkyl halides often decompose by (3-elimination. The a-bonded species formed by oxidative addition can react with alkenes and other unsaturated compounds to form new carbon-carbon bonds. The... 

The right sides of Eq. (3.21) can be employed as a measure of the chemical reactivity of both saturated and unsaturated compounds, which will be discussed in detail later. 

Mesomeric, like inductive, effects are permanent polarisations in the ground state of a molecule, and are therefore manifested in the physical properties of the compounds in which they occur. The essential difference between inductive and mesomeric effects is that while inductive effects can operate in both saturated and unsaturated compounds, mesomeric effects can operate only in unsaturated, especially in conjugated, compounds. The former involve the electrons in a bonds, the latter those in tt bonds and orbitals. Inductive effects are transmitted over only quite short distances in saturated chains before dying away, whereas mesomeric effects may be transmitted from one end to the other of quite large molecules provided that conjugation (i.e. delocalised tt orbitals) is present, through which they can proceed. 

Aromatics, olefins and in general, unsaturated compounds undergo hydrogenation reactions, usually unwanted due to their detrimental effect on the operating costs, derived from an excessive consumption of hydrogen. Aromatic saturation, however, is used in jet fuel to improve the smoke point and in diesel for cetane enhancement. In the case of gasoline, extreme hydrogenation leads to a deterioration of the fuel performance parameters. 

Hydrogen (reduction) alkenes, which are unsaturated compounds, add hydrogen to become saturated compounds ... 

Litol Also called Houdry-Litol. A process for making benzene by dealkylating other aromatic hydrocarbons. It is a complex process which achieves desulfurization, removal of paraffins and naphthenes, and saturation of unsaturated compounds, in addition to dealkylation. The catalyst contains cobalt and molybdenum. Developed by the Houdiy Process and Chemical Company and Bethlehem Steel Corporation. First installed by the Bethlehem Steel Corporation in 1964. Subsequently used at British Steel s benzole refinery, Teesside, England. 

Reagents which selectively retard certain chemical species can be incorporated into a thin-layer plate. Thus, silver nitrate, which forms weak 7t-complexes with unsaturated compounds, aids their separation from saturated compounds. 

Besides piperidine alkaloids, a total of 19 pyrrolidines have been found in the secretions of thief ants and fire ants of the genera Solenopsis and Monomorium. Among these, compounds 80-84 are simple pyrrolidines with two saturated linear all-carbon side chains only in Solenopsis latinode is there a secondary amine (82) and its methylated analog (85). One or two terminal unsaturations are present in compounds 86-91, which all possess a (hex-l-en)-6-yl chain and a 5-, 7-, or 9-carbon saturated chain. Compounds 93, 94, 96, 97, and 98 are the A-l-pyrrolines corresponding to pyrrolidines 80, 82, 90 (93 and 96 corresponding to 80, 94 to 82, and 97 and 98 to 90). 

---