Transcript Chapter 19. Aldehydes and Ketones

John E. McMurry
www.cengage.com/chemistry/mcmurry
Chapter 19
Aldehydes and Ketones:
Nucleophilic Addition Reactions
Paul D. Adams • University of Arkansas
Aldehydes and Ketones


Aldehydes (RCHO) and ketones (R2CO) are
characterized by the carbonyl functional group (C=O)
The compounds occur widely in nature as intermediates
in metabolism and biosynthesis
Why this Chapter?

Much of organic chemistry involves the chemistry
of carbonyl compounds

Aldehydes/ketones are intermediates in synthesis
of pharmaceutical agents, biological pathways,
numerous industrial processes

An understanding of their properties is essential
Functional Group Priority
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
Carboxylic Acids (3 O bonds, 1 OH)
Esters (3 O bonds, 1 OR)
Amides
Nitriles
Aldehydes (2 O bonds, 1H)
Ketones (2 O bonds)
Alcohols (1 O bond, 1 OH)
Amines
O
OH
Alkenes, Alkynes
Alkanes
OH
Ethers
Halides
2-ethyl-4-hydroxybutanoic acid
The parent will be determined based on the highest priority functional group.
19.1 Naming Aldehydes and
Ketones
Aldehydes are named by replacing the terminal –e of the
corresponding alkane name with –al
 The parent chain must contain the –CHO group
 The –CHO carbon is numbered as C1
 If the –CHO group is attached to a ring, use the suffix
carbaldehyde
Naming Aldehydes
O
H3C
O
H
pentanal
O
Cl
H3C
H
H
5-chloropentanal
CH3
H
CH3
O
2-ethylbutanal
O
H
Cl
Cl
m-chloro-benzaldehyde
5-chloro-2-methylbenzaldehyde
CH3
O
H
CH3
H3C
O
H
CH3
3,4-dimethylhexanal
O
CH3
5-methoxy-2-methylbenzaldehyde
Naming Ketones


Replace the terminal -e of the alkane name with –one
Parent chain is the longest one that contains the ketone
group

Numbering begins at the end nearer the carbonyl carbon
Ketones with Common
Names

IUPAC retains well-used but unsystematic names
for a few ketones
Naming Ketones
O
O
O
H3C
Cl
CH3
Cl
CH3
2-pentanone
CH3
1-chloro-3-pentanone
5-chloro-2-pentanone
O
F
O
CH3
H3C
CH3
4-ethylcyclohexanone
CH3
2-fluoro-5-methyl-4-octanone
Naming Ketones
O
O
O
O
Cl
butan-2-one
3,5-dimethylheptan-4-one
3-chloro-5-ethylheptan-4-one
O
O
O
but-3-en-2-one
OH
O
4-hydroxybutan-2-one
octane-2,7-dione
3-methylcyclopentanone
Cl
O
O
O
Cl
Br
7-bromo-3-chloro-4-methylcyclooctanone
cyclohex-2-en-1-one
3-chloro-5-ethyloct-7-en-1-yn-4-one
Ketones and Aldehydes as
Substituents

The R–C=O as a substituent is an acyl group, used with
the suffix -yl from the root of the carboxylic acid


CH3CO: acetyl; CHO: formyl; C6H5CO: benzoyl
The prefix oxo- is used if other functional groups are present
and the doubly bonded oxygen is labeled as a substituent on a
parent chain (lower priority functional group)
Ketones/Aldehydes as minor
FGs, benzaldehydes
O
H
O
O
O
O
OH
H
O
O
O
3-oxopentanal
3,4-dioxopentanal
3,4-dioxopentanoic acid
O
O
O
Cl
H
H
OH
H
O
benzaldehyde
O
H
O
3-chlorobenzaldehyde
O
O
H
3-oxopropanoic acid
O
2-formylbenzoic acid
O
O
H
methyl 3-oxopropanoate
O
O
methyl 3-oxobutanoate
Solubility of Ketones and
Aldehydes



Good solvent for alcohols
Lone pair of electrons on oxygen of carbonyl can accept a
hydrogen bond from O—H or N—H.
Acetone and acetaldehyde are miscible in water.
19.2 Preparing Aldehydes and
Ketones




Preparing Aldehydes
Oxidize primary alcohols using PCC (in dichloromethane)
Alkenes with a vinylic hydrogen can undergo oxidative
cleavage when treated with ozone, yielding aldehydes
Reduce an ester with diisobutylaluminum hydride (DIBAH)

Like LiAlH4
Preparing Ketones


Oxidize a 2° alcohol (See chapter on alcohols)
Many reagents possible: choose for the specific
situation (scale, cost, and acid/base sensitivity)
Ketones from Ozonolysis

Ozonolysis of alkenes yields ketones if one of the
unsaturated carbon atoms is disubstituted
Aryl Ketones by Acylation

Friedel–Crafts acylation of an aromatic ring with an acid chloride in
the presence of AlCl3 catalyst
O
+
Cl
AlCl3
Heat
O
Limitations of FC Acylation

Does not occur on rings with electron-withdrawing substituents or
basic amino groups
NH2
O
+
Cl
AlCl3
Heat
No Rxn
Mechanism of FC Acylation
Not subject to rearrangement like FC alkylation.
Methyl Ketones by Hydrating
Alkynes




Hydration of terminal alkynes in the presence of Hg2+
(catalyst: Section 9.4)
Markovnikov addition
Produces enol that tautomerizes to ketone
Works best with terminal alkyne
19.3 Oxidation of Aldehydes


CrO3 in aqueous acid oxidizes aldehydes to carboxylic
acids efficiently
Silver oxide, Ag2O, in aqueous ammonia (Tollens’
reagent) oxidizes aldehydes
Oxidation of Ketones




Ketones oxidize with difficulty
Undergo slow cleavage with hot, alkaline KMnO4
C–C bond next to C=O is broken to give carboxylic acids
Reaction is practical for cleaving symmetrical ketones
19.4 Nucleophilic Addition Reactions
of Aldehydes and Ketones


Nu- approaches
75° to the plane of
C=O and adds to C
A tetrahedral
alkoxide ion
intermediate is
produced
Nucleophiles


Nucleophiles can be negatively charged ( :Nu) or neutral
( :Nu) at the reaction site
The overall charge on the nucleophilic species is not
considered
Relative Reactivity of Aldehydes
and Ketones



Aldehydes are generally more reactive than ketones in
nucleophilic addition reactions
The transition state for addition is less crowded and lower
in energy for an aldehyde (a) than for a ketone (b)
Aldehydes have one large substituent bonded to the
C=O: ketones have two
Electrophilicity of Aldehydes and
Ketones



Aldehyde C=O is more polarized than ketone C=O
As in carbocations, more alkyl groups stabilize +
character
Ketone has more alkyl groups, stabilizing the C=O
carbon inductively
Reactivity of Aromatic
Aldehydes


Less reactive in nucleophilic addition reactions than
aliphatic aldehydes
Electron-donating resonance effect of aromatic ring makes
C=O less reactive electrophile than the carbonyl group of
an aliphatic aldehyde
19.5 Nucleophilic Addition of
H2O: Hydration


Aldehydes and ketones react with water to yield 1,1-diols
(geminal (gem) diols)
Hyrdation is reversible: a gem diol can eliminate water
Hydration of Aldehydes


Aldehyde hydrate is oxidized to a carboxylic acid by usual
reagents for alcohols
Relatively unreactive under neutral conditions, but can be
catalyzed by acid or base.
Hydration of Carbonyls
Acid catalyzed

Hydration occurs through the nucleophilic addition mechanism, with water
(in acid) or hydroxide (in base) serving as the nucleophile.
Base catalyzed
• The hydroxide ion attacks the carbonyl group.
• Protonation of the intermediate gives the hydrate.
Addition of H–Y to C=O


Reaction of C=O with H-Y, where Y is electronegative,
gives an addition product (“adduct”)
Formation is readily reversible (unstable alcohol)
19.6 Nucleophilic Addition of
HCN: Cyanohydrin Formation




Aldehydes and unhindered ketones react with HCN to
yield cyanohydrins, RCH(OH)CN
Addition of HCN is reversible and base-catalyzed,
generating nucleophilic cyanide ion, CNAddition of CN to C=O yields a tetrahedral intermediate,
which is then protonated
Equilibrium favors adduct
19.7 Nucleophilic Addition of Grignard
Reagents and Hydride Reagents: Alcohol
Formation

Treatment of aldehydes or ketones with Grignard
reagents yields an alcohol

Nucleophilic addition of the equivalent of a carbon anion,
or carbanion. A carbon–magnesium bond is strongly
polarized, so a Grignard reagent reacts for all practical
purposes as R:  MgX+.
Mechanism of Addition of
Grignard Reagents


Complexation of
C=O by Mg2+,
Nucleophilic
addition of R: ,
protonation by
dilute acid yields
the neutral
alcohol
Grignard
additions are
irreversible
because a
carbanion is not
a leaving group
Hydride Addition



Convert C=O to CH-OH
LiAlH4 and NaBH4 react as donors of hydride ion
Protonation after addition yields the alcohol
19.8 Nucleophilic Addition of Amines:
Imine and Enamine Formation


RNH2 adds to R’2C=O to form imines, R’2C=NR
(after loss of HOH)
R2NH yields enamines, R2NCR=CR2 (after loss
of HOH) (ene + amine = unsaturated amine)
Mechanism of Formation of
Imines






Primary amine adds
to C=O
Proton is lost from N
and adds to O to
yield an amino
alcohol
(carbinolamine)
Protonation of OH
converts it into water
as the leaving group
Result is iminium ion,
which loses proton
Acid is required for
loss of OH– too much
acid blocks RNH2
Optimum pH = 4.5
Imine Derivatives


Addition of amines with an atom containing a lone pair of
electrons on the adjacent atom occurs very readily,
giving useful, stable imines
For example, hydroxylamine forms oximes and 2,4dinitrophenylhydrazine readily forms 2,4dinitrophenylhydrazones

These are usually solids and help in characterizing liquid
ketones or aldehydes by melting points
Enamine Formation

After addition of
R2NH and loss of
water, proton is lost
from adjacent
carbon
19.9 Nucleophilic Addition of Hydrazine:
The Wolff–Kishner Reaction



Treatment of an
aldehyde or ketone
with hydrazine,
H2NNH2, and KOH
converts the
compound to an
alkane
Can be conducted
near room
temperature using
dimethyl sulfoxide
as solvent
Works well with both
alkyl and aryl
ketones
19.10 Nucleophilic Addition of
Alcohols: Acetal Formation



Alcohols are weak nucleophiles but acid promotes
addition forming the conjugate acid of C=O
Addition yields a hydroxy ether, called a hemiacetal
(reversible); further reaction can occur
Protonation of the –OH and loss of water leads to an
oxonium ion, R2C=OR+ to which a second alcohol adds to
form the acetal
Mechanism of Acetal
Formation
Mechanism of Acetal
Formation
Uses of Acetals



Acetals can serve as protecting groups for aldehydes and ketones
Aldehydes more reactive than ketones
It is convenient to use a diol to form a cyclic acetal (the reaction goes
even more readily)
19.11 Nucleophilic Addition of
Phosphorus Ylides: The Wittig Reaction




The sequence converts C=O to C=C
A phosphorus ylide adds to an aldehyde or ketone to yield
a dipolar intermediate called a betaine
The intermediate spontaneously decomposes through a
four-membered ring to yield alkene and
triphenylphosphine oxide, (Ph)3P=O
Formation of the ylide is shown below
Mechanism of the Wittig
Reaction
Product of Wittig Rxn




The Wittig reaction converts the carbonyl group into a new C═C double
bond where no bond existed before.
A phosphorus ylide is used as the nucleophile in the reaction.
Ylide usually CH2 or monosubstituted, but not disubstituted.
Unstabilized ylide tends to favor Z-alkene.
O
(Ph)3P+-CHCH3
H
THF
Z-alkene
+
(Ph)3P=O
19.13 Conjugate Nucleophilic Addition to
b-Unsaturated Aldehydes and Ketones


A nucleophile
can add to the
C=C double
bond of an ,bunsaturated
aldehyde or
ketone
(conjugate
addition, or 1,4
addition)
The initial
product is a
resonancestabilized
enolate ion,
which is then
protonated
Conjugate Addition of
Amines

Primary and secondary amines add to , b-unsaturated
aldehydes and ketones to yield b-amino aldehydes and
ketones
Conjugate Addition of Alkyl Groups:
Organocopper Reactions



Reaction of an ,b-unsaturated ketone with a lithium
diorganocopper reagent
Diorganocopper (Gilman) reagents form by reaction of 1
equivalent of cuprous iodide and 2 equivalents of
organolithium
1, 2, 3 alkyl, aryl and alkenyl groups react but not
alkynyl groups
Mechanism of Alkyl Conjugate
Addition: Organocopper Reactions


Conjugate nucleophilic addition of a diorganocopper
anion, R2Cu, to an enone
Transfer of an R group and elimination of a neutral
organocopper species, RCu
19.14 Spectroscopy of
Aldehydes and Ketones



Infrared Spectroscopy
Aldehydes and ketones show a strong C=O peak 1660 to
1770 cm1
aldehydes show two characteristic C–H absorptions in the
2720 to 2820 cm1 range.
C=O Peak Position in the IR
Spectrum

The precise position of the peak reveals the exact
nature of the carbonyl group
NMR Spectra of Aldehydes

Aldehyde proton signals are near  10 in 1H NMR distinctive spin–spin coupling with protons on the
neighboring carbon, J  3 Hz
13C


NMR of C=O
C=O signal is at  190 to  215
No other kinds of carbons absorb in this range
Mass Spectrometry – McLafferty
Rearrangement

Aliphatic aldehydes and ketones that have
hydrogens on their gamma () carbon atoms
rearrange as shown
Mass Spectroscopy:
-Cleavage


Cleavage of the bond between the carbonyl
group and the  carbon
Yields a neutral radical and an oxygencontaining cation