Contents
Leaving Cert Chemistry - Aldehydes and Ketones
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Aldehydes and Ketones
Aldehydes and ketones are
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
compounds i.e. they have a carbon-
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
double bond.
All aldehydes contain the -CHO group and are named with the ending
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
. Aldehydes are formed by the oxidation of
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
alcohols. Further oxidation causes the aldehyde to form a carboxylic
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
. The simplest aldehyde is methanal.
All ketones contain a carbonyl group attached to two
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
groups and are named with the ending
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
. Ketones are formed by the oxidation of secondary alcohols. The simplest ketone is
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
.
Aldehydes and ketones are found in nature and they are used as
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
in the manufacture of polymers.
The carbonyl group contains a
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
bond which has a significant effect on the
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
properties of aldehydes and ketones.The smaller aldehydes and ketones have much higher
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
points than alkanes of a similar molecular mass.This is due to the polar nature of the carbonyl group. However, aldehydes have lower boiling points than alcohols of similar relative
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
mass. This is due to the dipole-dipole attraction between the aldehde/ketone molecules not being as strong as the
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
bonding between the alcohol molecules.
The polar carbonyl group also causes smaller aldehydes and ketones to be
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
with water. This is because water forms
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
bonds with the carbonyl group.
The larger aldehydes and ketones are much less soluble in water due to the
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
size of the hydrocarbon part of the molecule. Aldehydes and ketones are soluble in non-polar solvents such as
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
.
An aldehyde can be
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
to a primary alcohol, while a ketone can be reduced to a secondary alcohol. This is done by reaction with hydrogen gas over a nickel
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
.
Aldehydes can be oxidised to
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
acids by either acidified potassium permanganate or
acid
-al
alkyl
boiling
carbonyl
carboxylic
catalyst
cyclohexane
Fehlings
hydrogen
increasing
miscible
molecular
-one
oxygen
physical
polar
primary
propanone
reduced
solvents
solution. Ketones cannot be oxidised.
Check
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