Carboxylic Acids

Carboxylic Acid Functional Group:

\chemfig{[,.6]R-C(=[6]O)-[,.6]OH}

(What is “R” ??)

Naming Carboxylic Acids

  • Use prefixes to indicate the number of carbon atoms.
  • Acids end with “-anoic acid.”

Example:

\chemfig{[,.4]-C(-[2])(-[6])-[,.6]C(-[2])(-[6])-[,.6]C(=[6,.6]O)-[,.6]OH}   is propanoic acid.

(3 carbons = “prop-” prefix, then add “-anoic acid” ending)

Physical Properties

  • Polar due to hydrogen bonding
  • Short carboxylic acids are soluble in water
  • High boiling points
  • Strong odors

Acid Behavior

In a solution, one of the hydrogen atoms can separate from a carboxylic acid and become H+:

\schemestart \chemfig{[,.5]CH_3C(=[6,,3]O)}-OH \arrow[,.7] \chemfig{[,.5]CH_3C(=[6,,3]O)-[,.6]O^{-}} + \chemfig{H^+} \schemestop

Anything that causes excess H+ ions to form in a solution is an acid. See Acid/Base notes.

Chemical Properties

Acids can react with alcohols to make esters:

\schemestart \chemname{\chemfig{[,.6]R-C(-OH)=[6]O}}{Carboxylic\\Acid} + \chemname{\chemfig{[,.6]R-OH}}{Alcohol} \arrow[,.7] \chemname{\chemfig{[,.6]R-C(-O-R)=[6]O}}{Ester} + \chemname{\chemfig{H_2O}}{Water} \schemestop

Carboxylic acids are an ingredient for making lots of interesting molecules in living things and in industry. See Wikipedia’s summary of carboxylic acid reactions for examples.

Some Important Carboxylic Acids

  • Ethanoic acid (more commonly known as acetic acid) is found in vinegar.

\chemfig{[,.6]-[,.4]C(-[2,.4])(-[6,.4])-C(=[6]O)-OH}

  • Butanoic acid (also known as butyric acid, derived from the word “butter”) gives vomit and rancid butter their lovely smells.

\chemfig{[,.6]-[,.4]C(-[2,.4])(-[6,.4])-C(-[2,.4])(-[6,.4])-C(-[2,.4])(-[6,.4])-C(=[6]O)-OH}

  • Amino acids such as alanine are what protein is made of.

\definesubmol{n}{-[,.7]N(-[2]H)-[,.7]C(-[2]H)} \definesubmol{a}{-[,.7]C(=[2]O)} \definesubmol{ala}{!n(-[6]CH_3)!a} \chemname{\chemfig{[,0.6]H!{ala}-OH}}{Alanine}

  • Stearic acid is a common fatty acid found in milk, beef fat, chocolate, and many other foods. It is also found in soaps, detergents, and cosmetics.

\chemname{ \definesubmol{a}{-C(-[2,.4])(-[6,.4])} \chemfig{[,.6]C(=[5]O)(-[3]HO)!a!a!a!a!a!a!a!a!a!a!a!a!a!a!a!a!a-[,.4]} }{Stearic Acid Structural Formula}

\chemname{ \definesubmol{a}{-[:30]-} \definesubmol{b}{-[:30]=[0]-} \chemfig{[:-30,0.6]HO-(=[6]O)!a!a!a!a!a!a!a!a-[:30]} }{Stearic Acid Stick Diagram}

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