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Summary - org chem 101
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organic chemistry notes about (carboxylic acids and their derivatives)
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iAcid R C OH R cook benzoicacid
s
o folic acid
IupacNamingofacid alkantoic acid cook
iii
H É OH cuz É on b CK COOH 2 napthalicacid
methanoicacid changeand propanoic acid
9 i
Ho É É on ethandioic acid oxalicacid
Naming priority Hoo cha coots propanedioicacid malonicacid
carboxylicacid aldhychorthlone alcohol attune Hooc cha cha coots butandioic acid succinicacid
cuzCI cha cook 3 hydroxybutanoicacid Hooc cha cook pentandioic acid glutaricacid
m
cook
H É cha cook 3 oxopropanoicacid
cook
coot coot colon
ohs É cha III cook 2 bromo 4oxopentanoicacid phthalicacid i terephtalicacid
common name forcarboxylic acid R É anacylgroup H É formylgroup
H É oh formicacid
m mn physicalproperties of carboxylicacid
Ctb cha cook propionicacid carboxylicacid are polarlikealcohol
cuz cha cha coots butyricacid theyformhydrogenbondwiththemselves
CHz cha cha cha coots valericacid
Bpcarboxylicacid alcohol aldehychztutone ether hydrocarbo
Pr 19 Iupac 3 bromopentanoicacid themorecookthehighertheboilingpoint
o
Y a common 13 bromo valeric acid as numberofcarbonincrease solubilitydecrease
Naming forcyclo alkane carboxylicacid
Acid protondonor
GOH
carboxylicacid H2O carboxylate anion
cyclopentancarboxylicacid cyclohexanecarboxylicacid R É oh H2o R Éo H
ka pka moreacidic u ka pka lessacidic
andcook
Y m
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