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8 Cards in this Set

  • Front
  • Back

physics properties

* High boiling point due to hydrogen bonding
* Soluble in water
* C=O at 1700 cm-1
* -OH at 3100 cm-1

COOH --> alcohol

1. reduction


2. LiAlH4


decarboxylation

1. occurs for beta-keto acids


2.

esterification

occurs under acidic conditions

COOH --> ester

1. esterification


2. occurs under acidic conditions


3. R-OH

halogenation of carboxylic acids

occurs at alpha carbon (2 position)


1. convert to enolizable form (w/ PBr)


2. enolize


3. halogenation


4. revert back to carboxylic acid (or hydrolysis)

COOH ---> acyl halide

PBr3

chemical properties

* dimerization occurs via H bonding
* acidity: pKa =5 (weak acid)
* ex: vinegar = dilute acetic acid
* substituents makes COOH stronger acid
* more stable carboxylate
* resonance: conj base stabilizes carboxylate ion