Quarterly Journal of the Chemical Society of London |
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Page 2580
... Table 1. Clearly , in this series of alums , reduction in AH , the heat of TABLE 1 . Struc- p ( mm . Hg ; Alum ture 25 ° ) ΔΗ ( cals . ) Alum Struc- ture p ( mm . Hg ; 25 ° ) ΔΗ ( cals . ) NaAl 20.48 10,763 NH , OHA1 ? 12.20 11,982 ΚΑΙ ...
... Table 1. Clearly , in this series of alums , reduction in AH , the heat of TABLE 1 . Struc- p ( mm . Hg ; Alum ture 25 ° ) ΔΗ ( cals . ) Alum Struc- ture p ( mm . Hg ; 25 ° ) ΔΗ ( cals . ) NaAl 20.48 10,763 NH , OHA1 ? 12.20 11,982 ΚΑΙ ...
Page 2824
... Table 2 . TABLE 2. Lags in the standard synthetic medium of strains isolated by the penicillin method after ultra - violet irradiation . No. of strains . Lag ( days ) 346 1-2 26 2-3 23 3-4 13 over 4 51 No growth in 2 wks . 68 Total 527 ...
... Table 2 . TABLE 2. Lags in the standard synthetic medium of strains isolated by the penicillin method after ultra - violet irradiation . No. of strains . Lag ( days ) 346 1-2 26 2-3 23 3-4 13 over 4 51 No growth in 2 wks . 68 Total 527 ...
Page 2922
... tables of standard values ( 4 ) . This compound has only one Me at C ( 1 ) Calc . from hedragonic lactone ( +194 ) by subtraction of A ( C : O - 2 ) ( +74 ) , see Table 7 . 2 , 13 , See Table 1. 19 , Reindel , Annalen , 1928 , 466 , 131 ...
... tables of standard values ( 4 ) . This compound has only one Me at C ( 1 ) Calc . from hedragonic lactone ( +194 ) by subtraction of A ( C : O - 2 ) ( +74 ) , see Table 7 . 2 , 13 , See Table 1. 19 , Reindel , Annalen , 1928 , 466 , 131 ...
Contents
ONE HUNDRED AND ELEVENTH ANNUAL GENERAL MEETING | 2449 |
483 | 2465 |
Mechanism of Substitution at a Saturated Carbon Atom Part XXXIII Kinetic | 2488 |
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acetic acid acetone acetyl acetyl chloride added alcohol alum aluminium aluminium bromide Amer ammonia anhydride aqueous atom benzene benzyl boiling Calc carbon Chem Chemical Chemistry chloroform chromatography colourless compound concentrated condensation cooled crystallised crystals decomp derivative dilute dissolved distilled dried ester ethanol ether ethyl acetate ethylene evaporated excess extracted filtered filtrate formed Found fraction gave give heated hydrate hydrochloric acid hydrogen bromide hydrogen chloride hydrolysis iodide isolated ketone L-iditol Lecture light petroleum b. p. lignin lithium aluminium hydride m. p. and mixed material method methyl mixed m. p. mixture molecular molecules needles nitrate obtained oxide phase phosphate polymer potassium hydroxide precipitated prepared present Professor pyridine reaction reflux requires residue retinene room temperature salt sample separated sodium hydroxide solid solution solvent stirred structure Table trifluoroiodomethane vapour pressure vitamin washed yellow yield