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Esters
Organic compound formed by the condensation reaction of a carboxylic acid and an alcohol.
O O R-C-OH + R-OH R-C-O-R’ + H2O
(ester)
Esters O R-C-O-R’
Naming: Parent chain “R” (including the C bonded to the
oxygens) Name the parent as an alkane Take off the “e”. Add –oate
Branches Identify alkyl group, R’Add alkyl name in front of parent chain.
Example O
C-C-O-C-C-CParent: ethane
ethanoate Branch: propylFinal name: propyl ethanoate
Example OC-C-C-C-O-C-C
Parent: butane butanoate
Branch: ethylFinal name: ethyl butanoate
Draw: pentyl hexanoate OC-C-C-C-C-C-O-C-C-C-C-C
Name: O
C-O-C-C-CParent: propane
propanoate Branch: methylFinal name: methyl propanoate
AminesOrganic compounds that are derivatives of
ammonia (NH3 ).
R-N-R” R’
Naming: Name the branches (R, R’, R”) in
alphabetical order; they can also be halogens.
Add the word amine at the end.
Primary amine(1 hydrogen is replaced by an alkyl group)
C-N-H H
methyl amine
Secondary amine(2 hydrogens are replaced by alkyl groups)
C-N-C-C H
ethyl methyl amine
Tertiary amine(3 hydrogens are replaced by alkyl groups)
C-N-C-C C-C-C
ethyl methyl propyl amine
Draw: pentyl propyl amine
C-C-C-C-C-N-C-C-C H