Aldehydes and ketones
1435-1436
2014-2015
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Aldehydes and ketones
Learning Objectives
Chapter eight introduces carbonyl compounds and reactions that involve a
nucleophilic attack at the carbonyl carbon in addition to the other topics.
By the end of this chapter the student will:
Know the structural differences between aldehydes and ketones
Know how to draw aldehydes and ketones
 know the common and IUPAC nomenclature of aldehydes and ketones
 Know the physical properties of aldehydes and ketones
Know how to synthesize an aldehyde or a ketone from a compound without
that
functionality.
 Know the different nucleophilic attack reactions at the carbonyl carbon and
the specific products formed in each case.
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Aldehydes and ketones
ALDEHYDES: STRUCTURE AND NOMENCLATURE
O
O
 General formula: RCHO or R-C-H
 Bond line formula
E
R
O
R
H
 The polarity of C=O
O
O
C
C
Nu
 The aldehyde group is always (terminal)at the end of a chain
Common Nomenclature Of Aldehydes
 Common name of aldehydes are derived from the common name of
the corresponding acid
 Some aliphatic aldehydes have common names which have to be
memorized.
Formaldehyde
145 Chem.
Acetaldehyde
Propionaldehyde
Butyraldehyde
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Aldehydes and ketones
 Some
aromatic aldehydes have common names such as:
OH O
O
H
Salicylaldehyde (o-Hydroxybenzaldehyde)
H
H3CO
4
Anisaldehyde (p-methoxybezaldehyde)
IUPAC Nomenclature
Select the longest continuous carbon chain that contains the H-C=O
group to get the name of the parent hydrocarbon, then replace the
ending e by the suffix –al
The CHO group is assigned the local 1 and takes precedence over
other functional groups that may present such as C=O(ketone),–OH,
C=C, CΞC, OR
For cyclic aldehydes in which the –CHO group is attached to the
ring, the suffix carbaldehyde is used.
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Aldehydes and ketones
Methanal
Ethanal
Propanal
Butanal
CHO
Cl
O
O
H
HO
H
O
OH
Cis-2-Hydroxy
cyclopentane
3-Chlorobutanal
3-Hydroxypropanal
2-Butenal
carbaldehyde
Aromatic aldehydes are usually designated as derivatives of the simplest aromatic aldehyde,
Benzaldehyde.
O
O
H
H
O2N
Benzaldehyde
4-Nitrobenzaldehyde
O
OH O
H
H
H3CO
2-Hydroxybenzaldehyde
4-Methoxybenzaldehyde
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Aldehydes and ketones
KETONES:STRUCTUR AND NOMENCLATURE
 General formula: RCOR’
(R and R’=alkyl or aryl)
 Common names of ketones derived by listing the alkyl substituents attached to the
carbonyl group in alphabetical order, followed by the word ketone.
 In common names carbon atoms near the carbonyl group are often designated using
Greek letters (α, ᵝ, ɣ , δ…..) beginning with carbon next the carbonyl group.
 When a complex molecules contains more than one of functional groups, an order
of precedence is used to determine the name.
 The functional group priority order in nomenclature system is as following:
Acid and derivatives > aldehyde > ketone > alcohol > amine > alkene > alkyne >
ether
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Aldehydes and ketones
O
H3C
C
O
CH3
Acetone
Dimethyl ketone
H3C
C
O
C6 H 5
Acetophenone
Methyl phenyl ketone
H3C
C
O
CH=CH 2 H5C6
3-Buten-2-one
Methyl vinyl ketone
C
C6H5
Benzophenone
Diphenyl ketone
IUPAC Nomencalture :
Select the longest continuous carbon chain that contains the C=O
group to get the name of the parent hydrocarbon, then replace the ending
e by the suffix –one
The chain is numbered in such a way as give the lowest number to the
C=O group.
The prefix of oxo is used if there are higher ranking functional groups
present.
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Aldehydes and ketones
Propanone
Phenyl ethanone
O
C2H5
C
3-Buten-2-one
O
Diphenylmethanone
O
OH
CHO
C2H5
Cyclopentylpropanone
3-Ethyl-2-hydroxycyclohexanone
5-Oxohexanal
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Aldehydes and ketones
Physical Properties OF Aldehydes And Ketones
 The carbonyl group is polar; with a partial negative charge on oxygen atom, and
partial positive charge on carbon atom.
 Because the polarity of the carbonyl group, aldehydes and ketones are polar
compounds.
C
C
O
O
1) Boiling and melting points
 Higher melting and boiling points compared to analogous alkanes due to they
show dipole-dipole attractions.


O
C
C
O


dipole-dipole attaraction
 These attractions although important, are not as strong as interactions due to
hydrogen bonding as a result, the boiling points of aldehydes and ketones are
higher than those of non polar alkanes, but lower than those of alcohols whose
molecules are connected together by H-bonds.
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Aldehydes and ketones
2) Solubility
Lower aldehydes and ketones are are more soluble than alkanes
but less soluble than alcohols in aqueous media

C

O


H
O


H


O
C
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Aldehydes and ketones
Preparation Of Aldehydes And ketones:
1- Oxidation of Alcohols
O
Cu/
H3C
CH3CH2OH
CH
or PCC
KMnO4
CH3CH2OH
O
H3C
C-OH
O
OH
Cu/
CH3CHCH3
or PCC
or KMnO4
, CrO3. HCl
PCC =
H3C
C-CH3
Pridinium Chloro chromate
N
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Aldehydes and ketones
2- Ozonolysis of Alkenes:
results in formation of aldehydes or ketones depending on
structure of the alkene used.
A
A
A
A
1] O3
2]Zn/ H2O
i) O3
ii) Zn / H2O
A
O
+
A
O
A
A
CH3CH2CHO + CH3CHO
two aldehydes
O
i) O3
ii) Zn / H2O
O
Diketone
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Aldehydes and ketones
3- Hydration Of Alkynes
4- Friedel Crafts Acylation
N.B: -COR group is m-director and deactivating towards electrophiles
O
O
+
R
Cl
AlCl3
R
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Aldehydes and ketones
Reactions Of Aldehydes And Ketones
the most common reactions are :Nucleophilic addition reactions
1- Reduction : Formation Of Alcohols
The reduction by NaBH4 , LiAlH4 ; the hydride ion H- is serve
as nucleophile.
NaBH4
O
or LiAlH4
H
or H2 / Pd
OH
NaBH4
O
or LiAlH4
OH
or H2 / Pd
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Aldehydes and ketones
2-Nucleophilic addition of Grignard reagent (formation of
alcohols)
 Addition of RMgX to formaldehyde gives 1◦ alc.
 Addition of RMgX to any other aldehyde gives 2◦ alc.
 Addition of RMgX to ketones gives 3◦ alc.
3- Oxidation reaction
Only aldehydes can be oxidized ketones resist oxidation
O
O
or
R
H
Ar
H
or K2Cr2O7
O
O
KMnO4
or
R
OH
Ar
OH
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Aldehydes and ketones
5-Addition of Hydrogen Cyanide: Formation Of Cynohydrins
O
R
OH
+ HCN
R'
R
R'
cyanohydrin
CN
O
CN
H
+
HCN
O
OH
B e n z a ld e h y d e c y a n o h y d rin
OH
+
HCN
CN
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Aldehydes and ketones
6- Addition Of Alcohols:
(old name)
Hemiacetal (new name)
(old name)
Acetal (new name)
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Aldehydes and ketones
7- Addition of Ammonia and Ammonia Derivatives
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Aldehydes and ketones
Exercises
1- The correct name of the following compound
is:
A) 3-hydroxyhexanal
B) 3-hydroxy-4-hexenal
C) 4-hydroxy-5-hexenal
D)3-hydroxy-1-hexenal
2- The structure of Acetal is:
O
A)
C2H5
B)
OH
C)
C2H5
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O
OH
O
C2H5
OH
O
C H
H 2 5
O
D)
C2H5
C2H5
O
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Aldehydes and ketones
3- Reaction of phenyhydrazine with carbonyl compounds (aldyhydes or
ketones) gives:
A) Oxime
B) Phenylhydrazone C) Imine
D) Hemiacetal
4 - Which of the following compounds has the highest boiling point?
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Aldehydes and ketones
Thank You for your kind attention !
Questions?
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