Why are esters and amides weaker carbon acids than ketones and acid fluorides? Contributions by resonance and inductive effects (Journal of Organic Chemistry (2009) 74, (7245) DOI: 10.1021/jo901225t);Why are esters and amides weaker carbon acids than ketones and acid fluorides? Contributions by resonance and inductive effects

Journal of Organic Chemistry

Volumn 74, Issue 19, 2009, Pages 7245-7253

  Fersner, Alexandra ^a   Karty, Joel M ^a   Mo, Yirong ^b  

^a ELON UNIVERSITY   (United States)

^b WESTERN MICHIGAN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; AMIDES; CARBON; DEPROTONATION; ENTHALPY; ESTERS; GASES; RESONANCE; WAVE FUNCTIONS;

CARBON ACID; COMPUTATIONAL METHODOLOGY; GASPHASE; INDUCTIVE EFFECTS; LOCALIZED WAVE FUNCTIONS; MODEL COMPOUND;

FLUORINE COMPOUNDS;

ACETAMIDE; ACETIC ACID; ACETONE; ACETYL FLUORIDE; AMIDE; ESTER DERIVATIVE; FLUORIDE; KETONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; ELECTRICITY; ENTHALPY; MATHEMATICAL MODEL; PROTON TRANSPORT; SOLVATION;

EID: 70349469709     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo902062h     Document Type: Erratum

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