Unsaturated, meaning

In contrast to alkanes, which have only single bonds, alkenes and alkynes have multiple bonds Alkenes are hydrocarbons that contain a carbon-carbon double bond, and alkynes are hydrocarbons that contain a carbon-carbon triple bond. Both groups of compounds are unsaturated, meaning that they have fewer hydrogens per carbon than the related alkanes. Ethylene (H2C = CH2), for example, has the formula C2H4, whereas ethane (CH3CH3) has the formula C2H6. 

What do saturated and unsaturated mean when applied to hydrocarbons Give an example of a saturated hydrocarbon and an example of an unsaturated hydrocarbon. 

What does unsaturated mean in the phrase margarine contains ... 

It involves the addition of a covalent molecule to the metal with cleavage of a covalent bond and can be considered a two-electron oxidation of the metal. One of the necessary conditions for this reaction is that the metal complexes to be oxidized should be coordinatively unsaturated. With the transition metal complexes, a saturated coordination number is determined by the configuration of the metal (/-electrons (five-coordination for ds metals, and four-coordination for d ° metals. If the complexes with these dn have less than these coordination numbers, they are said to be coordinatively unsaturated, and oxidative addition reaction may occur. In other words, co-ordinative unsaturation means that there are vacant sites on the complexes. 

Fats are typically straight long-chained hydrocarbons, and fatty acids are fats which have a carboxylic acid group at one end. Unsaturated means it contains a carbon-carbon double bond somewhere in its structure, while poly means it contains more than one of them. In fact, linoleic acid contains two C=C double... 

A type of lipid called a fatty acid is a carboxylic acid with a long hydrocarbon chain. Fatty acids can be saturated, meaning they contain the maximum number of hydrogen atoms, or unsaturated, meaning they contain one or more carbon-carbon double bonds. Saturated fatty acids experience greater inter-molecular forces, making them solid at room temperature, while unsaturated fatty acids are liquids. 

Separations based upon differences in the chemical properties of the components. Thus a mixture of toluene and anihne may be separated by extraction with dilute hydrochloric acid the aniline passes into the aqueous layer in the form of the salt, anihne hydrochloride, and may be recovered by neutralisation. Similarly, a mixture of phenol and toluene may be separated by treatment with dilute sodium hydroxide. The above examples are, of comse, simple apphcations of the fact that the various components fah into different solubihty groups (compare Section XI,5). Another example is the separation of a mixture of di-n-butyl ether and chlorobenzene concentrated sulphuric acid dissolves only the w-butyl other and it may be recovered from solution by dilution with water. With some classes of compounds, e.g., unsaturated compounds, concentrated sulphuric acid leads to polymerisation, sulphona-tion, etc., so that the original component cannot be recovered unchanged this solvent, therefore, possesses hmited apphcation. Phenols may be separated from acids (for example, o-cresol from benzoic acid) by a dilute solution of sodium bicarbonate the weakly acidic phenols (and also enols) are not converted into salts by this reagent and may be removed by ether extraction or by other means the acids pass into solution as the sodium salts and may be recovered after acidification. Aldehydes, e.g., benzaldehyde, may be separated from liquid hydrocarbons and other neutral, water-insoluble hquid compounds by shaking with a solution of sodium bisulphite the aldehyde forms a sohd bisulphite compound, which may be filtered off and decomposed with dilute acid or with sodium bicarbonate solution in order to recover the aldehyde. 

Other terms that mean the same thing as the index of hydrogen deficiency include elements of unsaturation sites of unsaturation and the sum of double bonds and rings... 

From Alcoholysis and Transesteriflcation. Metal alkoxides of higher, unsaturated, or branched alcohols are difficult to prepare directiy and are usually made from lower metal alkoxides by means of alcoholysis ... 

Sulfurized olefins (S2CI2 plus isobutene) are further reacted with S and Na2S to give products useful as extreme pressure lubricant additives (144,145). The reaction of unsaturated natural oils with sulfur monochloride gives resinous products known as Factice, which are useful as art-gum erasers and mbber additives (146,147). The addition reaction of sulfur monochloride with unsaturated polymers, eg, natural mbber, produces cross-links and thus serves as a means for vulcanizing mbber at moderate temperatures. The photochemical cross-linking of polyethylene has also been reported (148). 

Vinyllithium [917-57-7] can be formed direcdy from vinyl chloride by means of a lithium [7439-93-2] dispersion containing 2 wt % sodium [7440-23-5] at 0—10°C. This compound is a reactive intermediate for the formation of vinyl alcohols from aldehydes, vinyl ketones from organic acids, vinyl sulfides from disulfides, and monosubstituted alkenes from organic halides. It can also be converted to vinylcopper [37616-22-1] or divinylcopper lithium [22903-99-7], which can then be used to introduce a vinyl group stereoselectively into a variety of a, P-unsaturated systems (26), or simply add a vinyl group to other a, P-unsaturated compounds to give y, 5-unsaturated compounds. Vinyllithium reagents can also be converted to secondary alcohols with trialkylb o r ane s. 

EPM can be vulcanised radically by means of peroxides. A small amount of built-in third diene monomer in EPDM permits conventional vulcanisa tion with sulfur at the pendent sites of unsaturation. 

The inside of the convection tubes rarely foul, but occasionally the Hquid unsaturates in feedstocks tend to polymerize and stick to the walls and thus reduce the heat transfer. This soft coke is normally removed by mechanical means. In limited cases, the coke can also be burnt off with air and steam. Normally, the outside surface of the convection section fouls due to dust and particles in the flue gas. Periodically (6 to 36 months), the outside surface is cleaned by steam lancing. With Hquid fuel firing, the surface may require more frequent cleaning. 

The meaning of the word aromaticity has evolved as understanding of the special properties of benzene and other aromatic molecules has deepened. Originally, aromaticity was associated with a special chemical reactivity. The aromatic hydrocarbons were considered to be those unsaturated systems that underwent substitution reactions in preference to addition. Later, the idea of special stability became more important. Benzene can be shown to be much lower in enthalpy than predicted by summation of the normal bond energies for the C=C, C—C, and C—H bonds in the Kekule representation of benzene. Aromaticity is now generally associated with this property of special stability of certain completely conjugated cyclic molecules. A major contribution to the stability of aromatic systems results from the delocalization of electrons in these molecules. 

Wohf-Kishner reductions of a,jS-epoxy ketones give allylic alcohols, thus providing a means of reversing the arrangement in a,jS-unsaturated ketones or allylic alcohols. The reaction as first described by Wharton proceeds very readily (at room temperature in some instances) and the addition of strong base is unnecessary for example, the reduction of the epoxy ketone 143. 

The addition of primary amines to fluoroolefins under anhydrous conditions yields imines The hexafluoropropene dimer, perfluoro-2-methyl-2-pcntcne, and ten butylamine react to yield a mixture of two compounds m a 9 4 ratio [4] (equation 3) rather than just the major keteiiimme-imine, as previously reported [5] It IS claimed that this result is possible by means of isomerization to the terminally unsaturated difluoromethylene isomer prior to nucleophilic attack Secondary amines add to fluoroolefins under anhydrous conditions to give fluonnated ternary amines m good yields If the fluoroolefin is added to the amine without cooling the reaction mixture, or if an excess of the secondary armne is used, there is a tendency toward dehvdrofluonnation of the ternary amine The products... 

Heats of formation, molecular geometries, ionization potentials and dipole moments are calculated by the MNDO method for a large number of molecules. The MNDO results are compared with the corresponding MINDO/3 results on a statistical basis. For the properties investigated, the mean absolute errors in MNDO are uniformly smaller than those in MINDO/3 by a factor of about 2. Major improvements of MNDO over MINDO/3 are found for the heats of formation of unsaturated systems and molecules with NN bonds, for bond angles, for higher ionization potentials, and for dipole moments of compounds with heteroatoms. 

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