
TY  - JOUR
A1  - O'Conner, CJ 
A1  - McLennan, DJ 
A1  - Calvert, DJ 
A1  - Lomax, TD 
A1  - Porter, AJ 
A1  - Rogers, DA 
T1  - Substituent effects on the N.M.R. spectra of carboxylic acid derivatives. III. Correlation of <sup>13</sup>C N.M.R. spectra of <I>para</I> substituted acetanilides and 4'-nitrophenyl 4-substituted benzoates with infrared carbonyl stretching frequencies, <sup>1</sup>H N.M.R., rate and equilibrium data
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1984
VL  - 37
IS  - 3
SP  - 497
EP  - 510
KW  - 
UR  - https://doi.org/10.1071/CH9840497 
N2  - The 13C n.m.r. spectra of 17 monosubstituted benzenes, 14 para substituted acetanilides and ten 4'-nitrophenyl 4-substituted benzoates have been measured in (CD3)2SO and the chemical shifts have been compared with the infrared carbonyl stretching frequencies of the substrates (in CCl4), the 1H n.m.r. chemical shifts of protons close to the reactive site of protonation, rates of hydrolysis or aminolysis and literature values of the corresponding basicity constants and rate constants. The observed substituent chemical shifts are non-additive and this result has been discussed in terms of the electronic properties of -NHCOCH3 and -COOC6H4NO2. The 13C n.m.r. and the i.r. data have been treated by single parameter and dual substituent parameter linear free energy relationships and &#963;R values of best fit have been identified. Relative resonance and inductive contributions have been discussed. 
ER  -

