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Organic Chemistry
Carboxylic Acid
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Cards (29)
What are carboxylic acids?
compounds that all contain the functional group
'COOH-'
form
homologous
series
What is the
'COOH-'
group?
consists of
carbon
atoms that formed a
double
bond with a
lone oxygen
atom.
A
single
bond with an
oxygen
atom in an OH- group
Ending of a carboxylic acids ;
'oic
acids'
First 4 carboxylic acids
methanoic acids
ethanoic acids
propanoic acids
butanoic acids
Representing carboxylic acids
must show the
COOH-
functional group
Identifying carboxylic acids
look out for the
-COOH
groups
'anoic'
acid ending
Properties of carboxylic acids
Reacts like other
acids.
Carboxylic acids +
carbonates
-->
carbon dioxide
+
salt
and
water
2.
Dissolve
in
water
/ water-soluble and release
H+
ions
3.
Weak acids
= only
partially ionise
in water
Carboxylic
acids V Strong acids
Carboxylic
acids
have a
higher pH
(less acidic) than
aqueous
solutions of
strong
acids (sulphuric acid)
in the same CONCENTRATION
Esters
Have a functional group
-COO-
How are esters formed?
formed when
alcohol
+
carboxylic
acids -->
ester
+ (water)
Conditions needed for an ester to form
Presence of a
strong acid catalyst
Describe the formation of an ester
Carboxylic
acids react with
alcohols
in the presence of an acid
catalyst
to produce pleasant-smelling compounds called
esters.
Ester
pleasant-smelling, fruity organic compounds
Ethyl ethanoate
ethanol +
ethanoic
acid -->
ethyl
ethanoate
+ water
in the presence of an
acid catalyst
Limewater
calcium hydroxide
solution
Ca(Oh)2
Forms
calcium carbonate
,
CaCO3
when reacts with
water
+
carbon dioxide
Carboxylic acid + X carbonate
forms a salt,
-anoate
carbon dioxide
water
Esters
function group
-COO-
homologous
How are Esters formed?
alcohol
+
carboxylic acid
Conditions needed for Esters to form
presence of
strong
,
concentrated
acid catalyst
Reaction with alcohol and carboxylic acid
alcohol
+
carboxylic
acid -->
ester
+
water
in the presence of a strong, concentrated acid
catalyst
Example of Ethanol producing an Ester
Ethanol
+
ethanoic
acid -->
ethyl ethanoate
+
water
How to classify oxidising agent?
X[
O
]
General formula of a Carboxylic Acid
C(n-1)H(2n+1)COOH
Where n = -1
Properties of carboxylic acids
Boiling point
increases
with
increased
carbon chain length.
Viscosity increases with
increased
carbon chain length.
Solubility in water
decreases
with
increased
carbon chain length.
Why are carboxylic acids weaker than stronger acids such as Hydrochloric acid?
Carboxylic acids partially
ionise
in water /
aqueous
solution and does not fully
dissociate
it
hydrogen
ions.
What property makes Esters appropriate solvents?
pleasant
/sweet-smelling,
fruity
smells
used in
perfumes
Why are carboxylic acids also classified as a weak acids?
sometimes a
reversible
reaction
does not fully
dissociate
its
hydrogen
ions
Uses of esters
Flavourings
Perfumes
Solvents
Plastic
How to test between a carboxylic acid and an alcohol in a solution?
Add an
acid-base
indicator
if carboxylic acid present, indicator will turn
yellow-orange
Add a
hydrogen carbonate
if carboxylic acid present, will produce
efferservence
, indication of
carbon dioxide