Quarterly Journal of the Chemical Society of London, Volume 1 |
From inside the book
Results 1-3 of 64
Page 11
... parameters are listed in Table 1 . TABLE 1 SEARCH parameters 3 H18 9 8 4 Symmetry of the input model : 1 Cheshire group : * Z1 mmm 16 H26 15 H23 H28 H20 4,0 < π Parameter ranges : u < a / 2 6 H17 H21 W H27 ( 1 ) Parameter steps ...
... parameters are listed in Table 1 . TABLE 1 SEARCH parameters 3 H18 9 8 4 Symmetry of the input model : 1 Cheshire group : * Z1 mmm 16 H26 15 H23 H28 H20 4,0 < π Parameter ranges : u < a / 2 6 H17 H21 W H27 ( 1 ) Parameter steps ...
Page 442
... parameters a and B. As a consequence , assignments of а splittings carried out only by theoretical methods may lead to incorrect conclusions . Actually the parameters = TABLE 2 = 0.6 , Experimental and calculated McLachlan's spin ...
... parameters a and B. As a consequence , assignments of а splittings carried out only by theoretical methods may lead to incorrect conclusions . Actually the parameters = TABLE 2 = 0.6 , Experimental and calculated McLachlan's spin ...
Page 762
... parameters , are given subscripts and superscripts corresponding to those used above for the halogeno - substituents , are in Table 11 . TABLE 11 Interatomic distances * in nitrophenylacetic acids + 12+ " 17 12 ortho 2.5 2.85 2.5 4.1 ...
... parameters , are given subscripts and superscripts corresponding to those used above for the halogeno - substituents , are in Table 11 . TABLE 11 Interatomic distances * in nitrophenylacetic acids + 12+ " 17 12 ortho 2.5 2.85 2.5 4.1 ...
Contents
Physical organic chemistry | 1 |
Topochemistry Part XXX Crystal and molecular structures of chalcone | 11 |
Conformational studies Part I Crystal and molecular structures of cis12dipchlorobenzoyl and cis | 17 |
25 other sections not shown
Other editions - View all
Common terms and phrases
acetic acid activation added addition alcohol Amer angle appears aqueous assumed ation atoms base benzene bond bromination calculated carbon carbon tetrachloride Chem chemical Chemistry chloride compared complex compounds concentration conformation containing corresponding coupling crystal dependence derivatives determined difference DISCUSSION effect elimination energy equation error estimated ethanol ether exchange expected experimental experiments Figure formation fraction give given hydrogen increase indicators interaction intermediate involving isomer isotope kinetic measured mechanism method methyl mixture mole molecular molecule observed obtained occurs oxide oxygen parameters Phys plot position possible prepared present proton radical range rate constants ratio reaction reasonable relative reported requires respectively ring shifts shown shows similar sodium solution solvent spectra spectrum structure substituents suggested sulphuric Table temperature transition University values wave yield