17.carboxylic acids and derivatives. ( approx. lecture time: 4 lectures)

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17. CARBOXYLIC ACIDS AND DERIVATIVES. (approx. lecture time: 4 lectures) Topics covered: 17.1-17.2A-I,17.3-17.8,17.13. Some important carboxylic acids R H O R R O R OH O R X O R O R O R O X O Chapter 16 Chapter 17 Chapters 18 and 19 CH 3 CO 2 H OH O O CH 3 O CH 3 OH O OH O O O Na + _ HO O OH O H 3 C OH OH O OH O HO O OH

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17.CARBOXYLIC ACIDS AND DERIVATIVES. ( approx. lecture time: 4 lectures) Topics covered: 17.1-17.2A-I,17.3-17.8,17.13. Some important carboxylic acids. Carboxylic Acids are Weak Acids. pK a = 4.7. ( vineger ). Nomenclature. Synthesis of Carboxylic Acids. - PowerPoint PPT Presentation

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Page 1: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

R H

O

R R

O

R OH

O

R X

O

R

O

R

O

R

O

X

O

Chapter 16 Chapter 17 Chapters 18 and 19

17. CARBOXYLIC ACIDS AND DERIVATIVES. (approx. lecture time: 4 lectures)Topics covered: 17.1-17.2A-I,17.3-17.8,17.13.

Some important carboxylic acids

CH3CO2HOH

O

O

CH3O

CH3

OH

O

OH

O

O

O

Na+_

HO

O

OH

OH3C

OH

OH

OOHO

HO

O

OH

Page 2: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Carboxylic Acids are Weak Acids

pKa = 4.7

(vineger)

OH

OF

OH

OClor

which acid is stronger?

OH

O

or OH

O

F3C

Page 3: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Nomenclature

Page 4: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

CN

CH3CN CN

CN

NC

acetonitrile acrylonitrile benzonitrile 1,4-dicyanobenzene

NaCN

sodium cyanide

Page 5: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Synthesis of Carboxylic Acids

Page 6: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Synthesis of Carboxylic Acids via Carboxylation

using Grignard

reagent

Page 7: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Addition-Elimination at the Acyl Carbon (explains > 95% of the chemistry)

ORDER OF REACTIVITY:

> R-CN

Nitrileand acid

“Acyl transfer”

Page 8: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Interconversion of Carboxylic Acid Derivatives

In principle, any carboxylic acid derivative can be converted to another. In practice, acid chlorides (RCOCl), being the most reactive, are best for making them all (except nitriles)

interconversion between amide and nitrile:

This reaction is also an “acyl transfer”

All acyl transfers

Page 9: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Acid anhydrides are next in reactivity, and these can be converted to esters and amides:

All acyl transfers

Page 10: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Esterification of Carboxylic Acids

Forward reaction: EsterificationReverse reaction:Hydrolysis

(Acids and esters have an intimate relationship)

Page 11: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Esterification and Hydroylsis Mechanisms

Acid-catalyzed esterification and hydrolysis:

Base-catalyzed hydrolysis:

Page 12: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Hydrolysis of Amides(Basis of peptide hydrolysis and protein digestion)

Acid-catalyzed:

Base-catalyzed:

Page 13: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

R Cl

O

R O

O

OR'

R OR'

O

R OH

O

R NH2

OR C N> > > >

??

?

?

?

?

?

?

?

?

R-X

NaCN (SN2)

1. Mg/ether2. CO2

???

?

Ask yourself what interconversions are possible, indicating the reagent required and then a reaction mechanism.

You should know the ones in red !

Interconversion of Carboxylic Acid Derivatives

Page 14: 17.CARBOXYLIC ACIDS AND DERIVATIVES.     ( approx. lecture time:  4 lectures)

Some Important Amides

Kevlar(Nomex is the meta isomer)

TylenolPenicillin

Imodium (an opiod)

LSDCapsaicin

N

N(CH3)2O OH

ClHO

CH3O

HN

O

HO

HN CH3

O N

S

O

HN

R

O

H

CO2H

CH3

CH3

HN

N

Et2N O

CH3

H

H

N

NO

O

H

H

n

“bullet proof” vests