Dipole Moments in the Vapor State and Resonance Effects in Some Substituted Benzenes

1942 ◽  
Vol 64 (9) ◽  
pp. 2212-2216 ◽  
Author(s):  
Everett C. Hurdis ◽  
Charles P. Smyth
1957 ◽  
Vol 35 (12) ◽  
pp. 1575-1578 ◽  
Author(s):  
C. N. Ramachandra Rao ◽  
Werner H. Wahl ◽  
Edward J. Williams

not available


1974 ◽  
Vol 39 (11) ◽  
pp. 1527-1531 ◽  
Author(s):  
Lyman R. Caswell ◽  
Lily Y. Soo ◽  
Daisy H. Lee ◽  
Rosemary G. Fowler ◽  
Jo Anne B. Campbell

2018 ◽  
Vol 28 (4) ◽  
Author(s):  
Luis Salvatella

Electronic substituent effects are usually classified as inductive (through σ-bonds) and resonance effects (via π-bonds). The alkyl group has been usually regarded as aσ -electron donor substituent (+I effect, according to the Ingold’s classification). However, a σ-withdrawing, π-donor effect (-I + R pattern) allows explaining the actual electron-withdrawing behavior of alkyl groups when bound to sp³ carbon atoms as well as their well-known electron-releasing properties when attached to sp² or sp atoms. Alkyl substitution effects on several molecular properties (dipole moments, NMR, IR, and UV spectra, reactivity in gas phase and solution) are discussed.


1957 ◽  
Vol 30 (3) ◽  
pp. 218-222 ◽  
Author(s):  
Ichiro Miyagawa ◽  
Takehiko Chiba ◽  
Shoichi Ikeda ◽  
Yonezo Morino

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