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Chapter 11

This document discusses the structures, nomenclature, preparation methods, and reactions of aldehydes and ketones. It describes the IUPAC nomenclature used for aldehydes and ketones, including common examples. Methods for preparing aldehydes and ketones are oxidation of alcohols, hydration of alkynes, ozonolysis of alkenes, and Friedel-Crafts reactions. Characteristic reactions of aldehydes and ketones include addition reactions, such as cyanohydrin formation; catalytic hydrogenation to reduce to alcohols; Grignard addition; and acetal formation. Reactions involving the alpha hydrogens include aldol condensation and

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Biotechnology IIUM Kuantan
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439 views24 pages

Chapter 11

This document discusses the structures, nomenclature, preparation methods, and reactions of aldehydes and ketones. It describes the IUPAC nomenclature used for aldehydes and ketones, including common examples. Methods for preparing aldehydes and ketones are oxidation of alcohols, hydration of alkynes, ozonolysis of alkenes, and Friedel-Crafts reactions. Characteristic reactions of aldehydes and ketones include addition reactions, such as cyanohydrin formation; catalytic hydrogenation to reduce to alcohols; Grignard addition; and acetal formation. Reactions involving the alpha hydrogens include aldol condensation and

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Biotechnology IIUM Kuantan
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CHAPTER 11

ALDEHYDE AND KETONE


Structure of aldehyde and ketone
• Aldehyde and ketone = carbonyl compounds
• General formula CnH2nO

O O

C C
R H R R
aldehyde ketone
IUPAC Nomenclature for aldehydes and ketones

Compounds Structural formula IUPAC Nomenclature Commom Nomenclature

aldehydes HCOH methanal Formaldehyde

CH3COH ethanal Asetaldehyde

CH3CH2COH propanal Propionaldehyde

CH3CH2CH2COH butanal Butyraldehyde

CH3CH2CH2CH2COH pentanal valeraldehyde

ketones CH3COCH3 propanone Acetone

CH3COCH2CH3 2-butanone Methyethylketone

CH3COCH2CH2CH2CH3 2-pentanone n-propylmethylketone

CH3CH2COCH2CH3 3-pentanone Diethylketone

CH3CH(CH3)COCH3 3-methyl-2-butanone methylisopropylketone


Preparation of aldehydes and ketones
a) Hydration of alkynes
B) Ozonolysis of Alkenes
C) Friedel Crafts Reaction
D) Oxidation of alcohols
Tollens’ “Silver Mirror” Test
ADDITION REACTION OF ALDEHYDES AND
KETONES
1) Cyanohydrin Formation
- HCN is added to aldehyde/ketone to form
cyanohydrin or hydroxyl nitriles compound
- CN group is easily hydrolyzed to a carboxylic acid in
the presence of H2O/H+
2) Catalytic Hydrogenation: Reduction to ROH
3)Reduction to ROH
- NaBH or LiAlH are often used as a reducing agent and followed by
4 4
water/dilute acid to convert aldehyde/ketone to alcohols.
4)Grignard Addition- Preparation of ROH
5)Acetal Formation
-ROH is added to form hemiacetals then condence with a
second molecule of ROH to produce acetals
6)Addition of amines
REACTION INVOLVING ALPHA HYDROGENS
O
C C C C C
ε γ β α

• C=O is a strong electronwithdrawing group


• C=O can polarize the adjacent C-H bonds – making α-hydrogen weakly
acidic

δ−
O O
δ−
C C+ + OH- C C + H2O
δ -
δ+ H
O O-
C C C C
-
Enolate ion

O
-
O H+ OH
C
C C C C
C
H
Enol form
Keto
form

Tautomer = interconvertible structural isomers


Aldol Condensation
• Aldehyde or ketone molc is added to the C=O of another
by base initiated nucleophilic addition
CROSS ALDOL CONDENSATION
- Between 2 different carbonyl compounds.
- 1 of the molecule has no α-hydrogen

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