Posebna izdanja (Srpdka kraljevska akademija), Том 237 |
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Страница 8
... halides of the first main group do not react with lithium aluminum hydride , while those of the second group react unex- pectedly giving complex aluminum hydrides of the type M " ( AIH ) 2.897 , 910 , 1826 , 1937 The halides of indium ...
... halides of the first main group do not react with lithium aluminum hydride , while those of the second group react unex- pectedly giving complex aluminum hydrides of the type M " ( AIH ) 2.897 , 910 , 1826 , 1937 The halides of indium ...
Страница 103
... halides show the usual order of reactivity , i . e . , iodides > bromides > chlorides > flu- orides . This rule and the fact that the halogen function is less reactive than other polar functional groups have been successfully utilized ...
... halides show the usual order of reactivity , i . e . , iodides > bromides > chlorides > flu- orides . This rule and the fact that the halogen function is less reactive than other polar functional groups have been successfully utilized ...
Страница 134
... halides , 86 , 144 , 326 , 819 by the fact that the mode of ring opening in unsymmetrical epoxides is the same as in known bimolecular nucleophilic displacement reactions86 , 695 , 144 and by a comparison of reactivities of organic halides ...
... halides , 86 , 144 , 326 , 819 by the fact that the mode of ring opening in unsymmetrical epoxides is the same as in known bimolecular nucleophilic displacement reactions86 , 695 , 144 and by a comparison of reactivities of organic halides ...
Садржај
LITHIUM ALUMINUM HYDRIDE AS A REDUCING AGENT IN | 1 |
III | 7 |
Special Procedures and Preparation of Hydride Solutions | 13 |
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Чести термини и фразе
Acta action of lithium alcohols aldehydes aliphatic alkyl amides amino aromatic attack by lithium carbon atom carbonyl carbonyl group CH₂ CH₂O CH₂OH CH3 CH3 Chem Chemistry and Industry Chim chloride complex compounds containing converted corresponding cyclic derivatives diethyl ether dihydro diol double bond enol epoxides ester group ether solution ethylenic forcing conditions formation functional groups furnishes give H₂C H₂CO H₂O halides halogen Helv heterocyclic Hydride in Organic hydrocarbons hydrogen hydrogenolysis hydrolysis hydroxy hydroxyl group intermediate Karrer ketones lactams lactone LIAIHA lithium aluminum hydride lithium hydride means of lithium mechanism methyl mixture Monatsh nitriles nitro nitrogen nucleophilic obtained olefin optically active oxazolone oxide polar racemic react with lithium reaction reagent reducing agent reductions by lithium ring Rosenkranz saturated solvent steroids sulfinic acids sulfonate sulfonic acids temperatures tertiary tetrahydrofuran unsaturated VIII XVII XVIII XXIII yields