Barriers to rotation adjacent to double bonds. 3. The carbon-oxygen barrier in formic acid, methyl formate, acetic acid, and methyl acetate. The origin of ester and amide resonance

1987 ◽  
Vol 109 (20) ◽  
pp. 5935-5943 ◽  
Author(s):  
Kenneth B. Wiberg ◽  
Keith E. Laidig
2005 ◽  
Vol 247 (1-3) ◽  
pp. 55-60 ◽  
Author(s):  
Douglas M. Jackson ◽  
Nathan J. Stibrich ◽  
Jason L. McLain ◽  
Lillian D. Fondren ◽  
Nigel G. Adams ◽  
...  

1980 ◽  
Vol 45 (12) ◽  
pp. 3233-3240 ◽  
Author(s):  
Václav Svoboda ◽  
Věra Uchytilová ◽  
Vladimír Majer ◽  
Jiří Pick

Heats of vaporization of ethyl, propyl, butyl esters of formic acid, methyl, ethyl, propyl and butyl esters of acetic acid and methyl, ethyl and propyl esters of propionic acid were measured. These measurements reassume and complete data known from the literature. From the combination of values of heats of vaporization, the cohesive and vaporization internal energies of the set investigated were computed in the dependence on temperature.


2000 ◽  
Vol 193 (1) ◽  
pp. 16-28 ◽  
Author(s):  
M.A.Natal Santiago ◽  
M.A. Sánchez-Castillo ◽  
R.D. Cortright ◽  
J.A. Dumesic

1959 ◽  
Vol 37 (2) ◽  
pp. 389-402 ◽  
Author(s):  
P. Kebarle ◽  
F. P. Lossing

The Hg(3P1) photosensitized decomposition of formic acid proceeds by two intramolecular rearrangement reactions, leading respectively to H2O and CO, and to H2 and CO2. No free radicals are produced. The decomposition reactions of methyl formate and of acetic acid proceed predominantly by the formation of free radicals, but intramolecular rearrangements also occur to a significant extent. For both these latter compounds the evidence suggests the occurrence of two modes of dissociation into free radicals:[Formula: see text]No evidence for the alternative mode of dissociation[Formula: see text]was found.


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