Journal of the Chemical Society, Part 1Chemical Society., 1942 |
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Results 1-3 of 87
Page 22
... alcohols recalls the cyclic structure for xy - dimethylallyl alcohol discussed by Hills , Kenyon , and Phillips ( J. , 1936 , 576 ) as a result of parachor determinations . We have therefore re - examined the question of the parachors ...
... alcohols recalls the cyclic structure for xy - dimethylallyl alcohol discussed by Hills , Kenyon , and Phillips ( J. , 1936 , 576 ) as a result of parachor determinations . We have therefore re - examined the question of the parachors ...
Page 23
... alcohol ( M , 88 ) increases by 1-2 units between 15 ° and 40 ° , whereas that of ay - dimethylallyl alcohol ( M , 86 ) increases by only 0.2 unit in the same temperature range . The low parachors of allyl alcohol and its a- and y ...
... alcohol ( M , 88 ) increases by 1-2 units between 15 ° and 40 ° , whereas that of ay - dimethylallyl alcohol ( M , 86 ) increases by only 0.2 unit in the same temperature range . The low parachors of allyl alcohol and its a- and y ...
Page 24
... alcohol and the anionotropic isomeride are formed , we have applied to the product the method of analysis described above . It is found that , starting with ( + ) - y - methyl - a - ethylallyl alcohol , the product of hydrolysis of its ...
... alcohol and the anionotropic isomeride are formed , we have applied to the product the method of analysis described above . It is found that , starting with ( + ) - y - methyl - a - ethylallyl alcohol , the product of hydrolysis of its ...
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Common terms and phrases
absorption acetone acidified alkaline aluminium amine ammonia anhydride aqueous atoms autoxidation base benzene boiling bromine Calc carbon carbonisation CH₂ Chem Chemical chloramine-T chloroform colour colourless needles compound concentrated condensation containing cooled copper crystallised from alcohol crystals decomp decomposition derivative dilute dissolved distilled double bond dried ester evaporated excess experimental extracted with ether filtered filtrate formation formed Found fraction gave glacial acetic acid H₂O heated hydrocarbon hydrochloric acid hydrogen chloride hydrolysis hydroperoxide hydroxyl ions isolated kations ketone light petroleum liquid melting method methyl alcohol methyl iodide micelles mixed m. p. mixture molecular molecule obtained oxidation oxidised oxygen peroxide potassium hydroxide precipitate prepared present prisms pyridine R₁ R₂ reaction refluxed requires residue salt separated sodium hydroxide solasodine solid soluble solvent substance sulphate sulphide sulphuric acid temperature thioindoxyl unsaturated washed water-bath yellow needles yield