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Selenium. The substance is heated with a large excess of selenium at 280-350° for 36-48 hours. Better yields (and less side reactions) are usually obtained than with sulphur, but, owing to the higher temperature, rearrangements are more likely. Oxygen-containing groups are particularly prone to elimination. [Pg.948]

Solvation increases solubility above predicted values. When the components of a solution possess an abnormally large attraction for each other, solvates are formed. Thus certain oxygen-containing compounds have a great tendency to form hydrates, thus contributing to increased water solubility hydrogen bondir also plays an important role. [Pg.1048]

Concentrated sulphuric acid. The paraffin hydrocarbons, cych-paraffins, the less readily sulphonated aromatic hydrocarbons (benzene, toluene, xylenes, etc.) and their halogen derivatives, and the diaryl ethers are generally insoluble in cold concentrated sulphuric acid. Unsaturated hydrocarbons, certain polyalkylated aromatic hydrocarbons (such as mesitylene) and most oxygen-containing compounds are soluble in the cold acid. [Pg.1049]

Many oxygen-containing compounds dissolve because of the formation of oxonium salts the latter are readily decomposed (hydrolysed) by pouring the acid into ice water. [Pg.1050]

The production of both an alcohol and the sodium salt of an acid might easily be confused with the hydrolysis products of an ester (in the above instance benzyl benzoate). Such an error would soon be discovered (e.g., by reference to the b.p. and other physical properties), but it would lead to an unnecessary expenditure of time and energy. The above example, however, emphasises the importance of conducting the class reactions of neutral oxygen-containing compounds in the proper order, viz., (1) aldehydes and ketones, (2) esters and anhydrides, (3) alcohols, and (4) ethers. [Pg.1063]

If the unknown neutral, oxygen-containing compound does not give the class reactions for aldehydes, ketones, esters and anhydrides, it is probably... [Pg.1065]

Neutral oxygen-containing compounds in Solubility Groups I, II and V which either contain the CHjCO— group attached to H, alkyl, aryl, or ester H R... [Pg.1068]

The weakly basic 2-aminothiazoles are most readily diazotized in concentrated solutions of oxygen containing acids such as sulfuric acid, 40 to 50% (322-326) fiuoroboric phosphoric acids (589) phosphoric acid (327, 328) and mixtures of phosphoric and nitric acid (74. 322, 323. 329-331). From strong acid solutions, solid diazonium salts can be isolated (34, 332. 333). [Pg.66]

You have just seen that cyclic halonmm ion intermediates are formed when sources of electrophilic halogen attack a double bond Likewise three membered oxygen containing rings are formed by the reaction of alkenes with sources of electrophilic oxygen... [Pg.260]

The next several chapters deal with the chemistry of various oxygen containing func tional groups The interplay of these important classes of compounds—alcohols ethers aldehydes ketones carboxylic acids and derivatives of carboxylic acids— IS fundamental to organic chemistry and biochemistry... [Pg.623]

This chapter is a transitional one It ties together much of the material encountered earlier and sets the stage for our study of other oxygen containing functional groups m the chapters that follow... [Pg.623]

The melting points and boiling points of carboxylic acids are higher than those of hydro carbons and oxygen containing organic compounds of comparable size and shape and indicate strong mtermolecular attractive forces... [Pg.794]

Not all carotenoids are hydrocarbons Oxygen containing carotenes called xantho phylls which are often the pigments responsible for the yellow color of flowers are espe cially abundant... [Pg.1101]

Bivalent Sulfur. The prefix thio, placed before an affix that denotes the oxygen-containing group or an oxygen atom, implies the replacement of that oxygen by sulfur. Thus the suffix -thiol denotes — SH, -thione denotes —(C)=S and implies the presence of an =S at a nonterminal carbon atom, -thioic acid denotes [(C)=S]OH [(C)=0]SH (that is, the O-substituted acid and the 5-substi-... [Pg.37]

Salts are formed as with oxygen-containing compounds. For example, C2H5 — S—Na is named either sodium ethanethiolate or sodium ethyl sulfide. If mercapto- has been used as a prefix, the salt is named by use of the prefix sulfido- for —S . [Pg.38]

Molecular oxygen contains two unpaired electrons and has the distinction of being capable of both initiating and inhibiting polymerization. It functions in the latter capacity by forming the relatively unreactive peroxy radical ... [Pg.396]

Furan can be catalyticaHy oxidized in the vapor phase with oxygen-containing gases to maleic anhydride (93). Oxidation with bromine or in an electrochemical process using bromide ion gives 2,5-dimethoxy-2,5-dihydrofuran [332-77-4] (19) which is a cycHc acetal of maleic dialdehyde (94—96). [Pg.81]

Table 4. Boron Trifluoride Adducts with Oxygen-Containing Compounds... Table 4. Boron Trifluoride Adducts with Oxygen-Containing Compounds...

See other pages where Containers oxygen is mentioned: [Pg.97]    [Pg.213]    [Pg.387]    [Pg.732]    [Pg.2722]    [Pg.2806]    [Pg.890]    [Pg.1048]    [Pg.1050]    [Pg.351]    [Pg.497]    [Pg.648]    [Pg.70]    [Pg.74]    [Pg.124]    [Pg.161]    [Pg.161]    [Pg.268]    [Pg.400]    [Pg.473]    [Pg.475]    [Pg.476]    [Pg.476]    [Pg.54]    [Pg.379]    [Pg.484]    [Pg.499]    [Pg.47]    [Pg.432]    [Pg.493]    [Pg.115]    [Pg.479]    [Pg.479]   
See also in sourсe #XX -- [ Pg.288 ]




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