Journal of the Chemical SocietyThe Society., 1964 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Page 4795
... mole ) , 76 total 47 < 16 3 1 2 I bicumyl b cumene ( 3 % ) PhCONH ) , ( 0-01 mole ) , benz- 71 total 100 trace 22 4 Ph2 ene ( 2 % ) B. Photolytic Decompositions of Azodibenzoyl 01 mole , benzene ( 1 % ) , 7 hr . , 80 ° 51 total 8 none b ...
... mole ) , 76 total 47 < 16 3 1 2 I bicumyl b cumene ( 3 % ) PhCONH ) , ( 0-01 mole ) , benz- 71 total 100 trace 22 4 Ph2 ene ( 2 % ) B. Photolytic Decompositions of Azodibenzoyl 01 mole , benzene ( 1 % ) , 7 hr . , 80 ° 51 total 8 none b ...
Page 5048
... ( mole ) mole ) mole ) mole ) PH Q ( cal . ) ( 10-5 mole ) [ M penten ] 2+ [ M penten H ] 3 + ( 10-5 mole ) Qez ( cal . ) Manganese 938 947 25 9.6 85.5 938 2-3 942 951 25 85.9 942 2.4 Iron 9184 923 327 9.9 93.4 918 4.8 1000 a 1006 345 ...
... ( mole ) mole ) mole ) mole ) PH Q ( cal . ) ( 10-5 mole ) [ M penten ] 2+ [ M penten H ] 3 + ( 10-5 mole ) Qez ( cal . ) Manganese 938 947 25 9.6 85.5 938 2-3 942 951 25 85.9 942 2.4 Iron 9184 923 327 9.9 93.4 918 4.8 1000 a 1006 345 ...
Page 5054
... mole ) ( 10-5 mole ) ( cal . ) Qcz . ( cal . ) Tetren ( 10-5 mole ) HCI Q Qez . ( 10-5 mole ) ( cal . ) ( cal . ) 1989 1990 219.2 12.3 631 1891 206.3 7-0 2001 2001 220.9 12.3 485 1944 197.0 6.1 2004 2001 221.0 12.3 476 1903 193.2 5.8 ...
... mole ) ( 10-5 mole ) ( cal . ) Qcz . ( cal . ) Tetren ( 10-5 mole ) HCI Q Qez . ( 10-5 mole ) ( cal . ) ( cal . ) 1989 1990 219.2 12.3 631 1891 206.3 7-0 2001 2001 220.9 12.3 485 1944 197.0 6.1 2004 2001 221.0 12.3 476 1903 193.2 5.8 ...
Contents
NO PAGE | 4677 |
Water in hydrates Part II Light and heavy water and sulphur dioxide | 4684 |
sulphurcontaining antioxidants | 4692 |
Copyright | |
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absorption acetic acid acetone added adduct aluminium chloride Amer amine anisole aqueous aromatic atoms band benzene bond boron trifluoride bromide Calc carbon cation CH₂ Chem chloride chromatography cm.¹ complex compound concentration constant cooled crystallised crystals decaborane decomposition derivatives dilute dimethyl dioxide distilled dried eluted ester ethanol ether evaporated experimental extracted filtered formation formed Found fraction gave give H₂O hydride hydrochloric acid hydrogen hydrolysis hydroxide hydroxyl infrared infrared spectrum iodide isolated isomer ketone ligand light petroleum b. p. lithium aluminium hydride methyl methylene mixture mole molecular molecules needles nitrate nitrogen obtained olefin oxide penten peroxide phenol potassium precipitate prepared pressure protons pyridine radical ratio reaction recrystallised reduced requires residue resonance room temperature salt sample silver sodium sodium hydroxide solid solubility solution solvent spectra structure sulphuric Table values washed yellow yield