ORGANIC CHEMISTRY
LESSON 1: CARBOXYLIC ACIDS
CARBOXYLIC ACID FUNCTIONAL GROUP
• CARBOXYLIC ACID GROUP IS A CARBON DOUBLE BONDED TO AN OXYGEN (CARBONYL)
ATOM AND THE SAME CARBON BONDED TO A HYDROXY (ALCOHOL) GROUP
CARBOXYLIC ACIDS
• IMPORTANT IN OXIDATION REACTIONS
• CHARACTERIZED BY THEIR CARBONYL (COOH) GROUP
• IN CITRUS FRUITS
• LACTIC ACID IN MUSCLES
NAMING CARBOXYLIC ACIDS
DROPPING THE “E” ON THE CHAIN AND ADDING “OIC ACID”
NAME OFF MAIN CHAIN LIKE ALCOHOLS, KETONES AND ALDEHYDES WITH “ACID” AT THE END
EXAMPLE
• ETHANOIC ACID
EXAMPLES
Pentanoic acid
heptanoic acid
POLY-CARBOXYLIC ACIDS
propane-1,3-dioic acid
- Name the Same as last three
functional groups
- Keep the “e” O
H C
CH2 C
OH
O
O
AROMATIC CARBOXYLIC ACIDS
• DROP THE “ENE” ENDING AND ADD “OIC ACID”
• BENZOIC ACID
C
CH
CH
CH
C
H
C
H
C
OH
O
PROPERTIES
• HAVE HIGHEST PRIORITY OF ALL FUNCTIONAL GROUPS
• HAVE PROPERTIES SIMILAR TO ACIDS
• BOTH HYDROGEN BONDING AND DIPOLE FORCES
• BOILING POINTS EVEN LARGER THAN ALCOHOLS
ORGANIC CHEMISTRY
LESSON 2: ESTERS AND ESTERIFICATION
ESTER FUNCTIONAL GROUP
• ESTER FUNCTIONAL GROUP IS A CARBONYL GROUP BONDED TO AN OXYGEN ATOM
• OXYGEN ATOM IS BONDED TO ANOTHER HYDROCARBON CHAIN (LIKE ETHER)
ESTERS
• FORMED IN CONDENSATION/ESTERIFICATION REACTIONS
• GIVE OFF SCENTS (FLOWERS, PERFUMES)
• FLAVOURING TO FOODS
NAMING ESTERS
• THE NAME OF THE GROUP ATTACHED TO OXYGEN COMES FIRST AND NAMED AS AN ALKYL
GROUP
• THE GROUP NAME IS SEPARATE FROM THE MAIN CHAIN
• CHANGING THE ENDING OF THE MAIN CHAIN TO “OATE”
• CARBONYL CARBON WILL HAVE PRIORITY
EXAMPLE
Notice these names are TWO words
EXAMPLE
C
H3 C
H
C O
O
CH2
CH2
C
H3
CH3
Propyl 2-methylpropanoate
EXAMPLES
PROPERTIES
• NOT AS HIGH OF MELTING POINT AS ALCOHOLS
• DIPOLE-DIPOLE FORCES
Carboxylic acid and ester naming lesson.

Carboxylic acid and ester naming lesson.