1. Structure of Carboxylic Acid Derivatives

2. Electron Delocalization and the Carbonyl Group The main structural feature that distinguishes acyl chlorides, anhydrides, esters, and amides is the interaction of the substituent with the carbonyl group. It can be represented in resonance terms as: RC O X RC O X + RC O X +––

3. Electron Delocalization and the Carbonyl Group The extent to which the lone pair on X can be delocalized into C=O depends on: 1) the electronegativity of X 2) how well the lone pair orbital of X interacts with the  orbital of C=O RC O X RC O X + RC O X +––

4. Orbital overlaps in carboxylic acid derivatives  orbital of carbonyl group

5. Orbital overlaps in carboxylic acid derivatives lone pair orbital of substituent

6. Orbital overlaps in carboxylic acid derivatives electron pair of substituent delocalized into carbonyl  orbital

7. acyl chlorides have the least stabilized carbonyl group delocalization of lone pair of Cl into C=O group is not effective because C—Cl bond is too long Acyl Chlorides C O R Cl C O R Cl + –

8. RCClO least stabilized C=O most stabilized C=O

9. lone pair donation from oxygen stabilizes the carbonyl group of an acid anhydride the other carbonyl group is stabilized in an manner by the lone pair Acid Anhydrides C R O O C O R O +–C R O O C R

10. RCOCR'OO least stabilized C=O most stabilized C=O RCClO

11. lone pair donation from oxygen stabilizes the carbonyl group of an ester stabilization greater than comparable stabilization of an anhydride Esters +–C R O OR' O C R OR'

12. RCOCR'OO RCClO RCOR'O least stabilized C=O most stabilized C=O

13. lone pair donation from nitrogen stabilizes the carbonyl group of an amide N is less electronegative than O; therefore, amides are stabilized more than esters and anhydrides Amides +–C R O NR' 2 O C R NR' 2

14. amide resonance imparts significant double-bond character to C—N bond activation energy for rotation about C—N bond is 75-85 kJ/mol C—N bond distance is 135 pm in amides versus normal single-bond distance of 147 pm in amines Amides +–C R O NR' 2 O C R NR' 2

15. RCOCR'OO RCClO RCOR'O RCNR' 2 O least stabilized C=O most stabilized C=O

16. very efficient electron delocalization and dispersal of negative charge maximum stabilization Carboxylate ions O C R – O –C R O O

17. RCOCR'OO RCClO RCOR'O RCNR' 2 O RCO – O least stabilized C=O most stabilized C=O

18. Reactivity is related to structure: RCOCR'OO RCClO RCOR'O RCNR' 2 OStabilization Relative rate of hydrolysis very small 10 11 small 10 7 large < 10 -2 moderate1.0 The more stabilized the carbonyl group, the less reactive it is.

19. RCOCR'OO RCClO RCOR'O RCNR' 2 O RCO – O most reactive least reactive

20. Nucleophilic Acyl Substitution In general: O C R X + HY O C R Y + HX Reaction is feasible when a less stabilized carbonyl is converted to a more stabilized one (more reactive to less reactive).

21. General Mechanism for Nucleophilic Acyl Substitution involves formation and dissociation of a tetrahedral intermediate O C R X HYHYHYHY C ROHX Y O C R Y -HX

22. RCOCR'OO RCClO RCOR'O RCNR' 2 O RCO – O most reactive least reactive a carboxylic acid derivative can be converted by nucleophilic acyl substitution to any other type that lies below it in this table