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11.3 Alcohols, Acids, and Esters

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  • Alcohols

    An alcohol is an organic compound with a hydroxyl (OH) functional group on an aliphatic carbon atom. Because OH is the functional group of all alcohols, we often represent alcohols by the general formula ROH, where R is an alkyl group. Alcohols are common in nature. Most people are familiar with ethyl alcohol (ethanol), the active ingredient in alcoholic beverages, but this compound is only one of a family of organic compounds known as alcohols. The family also includes such familiar substances as cholesterol and the carbohydrates. Methanol (CH3OH) and ethanol (CH3CH2OH) are the first two members of the homologous series of alcohols.

    Alcohols with one to four carbon atoms are frequently called by common names, in which the name of the alkyl group is followed by the word alcohol:

    nomenclature.jpg

    According to the International Union of Pure and Applied Chemistry (IUPAC), alcohols are named by changing the ending of the parent alkane name to -ol.

    Alcohols can be considered derivatives of water (H2O; also written as HOH).

    water.jpg

    Like the H–O–H bond in water, the R–O–H bond is bent, and alcohol molecules are polar. This relationship is particularly apparent in small molecules and reflected in the physical and chemical properties of alcohols with low molar mass. Replacing a hydrogen atom from an alkane with an OH group allows the molecules to associate through hydrogen bonding (Figure \(\PageIndex{1}\)).

    Figure \(\PageIndex{1}\): Intermolecular Hydrogen Bonding in Methanol. The OH groups of alcohol molecules make hydrogen bonding possible.

    Recall that physical properties are determined to a large extent by the type of intermolecular forces. Table \(\PageIndex{1}\) lists the molar masses and the boiling points of some common compounds. The table shows that substances with similar molar masses can have quite different boiling points.

    Table \(\PageIndex{1}\): Comparison of Boiling Points and Molar Masses
    Formula Name Molar Mass Boiling Point (°C)
    CH4 methane 16 –164
    HOH water 18 100
    C2H6 ethane 30 –89
    CH3OH methanol 32 65
    C3H8 propane 44 –42
    CH3CH2OH ethanol 46 78
    C4H10 butane 58 –1
    CH3CH2CH2OH 1-propanol 60 97

    Alkanes are nonpolar and are thus associated only through relatively weak dispersion forces. Alkanes with one to four carbon atoms are gases at room temperature. In contrast, even methanol (with one carbon atom) is a liquid at room temperature. Hydrogen bonding greatly increases the boiling points of alcohols compared to hydrocarbons of comparable molar mass. The boiling point is a rough measure of the amount of energy necessary to separate a liquid molecule from its nearest neighbors. If the molecules interact through hydrogen bonding, a relatively large quantity of energy must be supplied to break those intermolecular attractions. Only then can the molecule escape from the liquid into the gaseous state.

    Alcohols can also engage in hydrogen bonding with water molecules (Figure \(\PageIndex{2}\)). Thus, whereas the hydrocarbons are insoluble in water, alcohols with one to three carbon atoms are completely soluble. As the length of the chain increases, however, the solubility of alcohols in water decreases; the molecules become more like hydrocarbons and less like water. The alcohol 1-decanol (CH3CH2CH2CH2CH2CH2CH2CH2CH2CH2OH) is essentially insoluble in water. We frequently find that the borderline of solubility in a family of organic compounds occurs at four or five carbon atoms.

    Figure \(\PageIndex{2}\): Hydrogen Bonding between Methanol Molecules and Water Molecules. Hydrogen bonding between the OH of methanol and water molecules accounts for the solubility of methanol in water.

    Carboxylic Acids

    Carboxylic acids occur widely in nature, often combined with alcohols or other functional groups, as in fats, oils, and waxes. They are components of many foods, medicines, and household products (Figure \(\PageIndex{1}\)). Not surprisingly, many of them are best known by common names based on Latin and Greek words that describe their source.

    15.1.jpg
    Figure \(\PageIndex{1}\): Carboxylic Acids in the Home. Carboxylic acids occur in many common household items. (a) Vinegar contains acetic acid, (b) aspirin is acetylsalicylic acid, (c) vitamin C is ascorbic acid, (d) lemons contain citric acid, and (e) spinach contains oxalic acid. © Thinkstock

    The simplest carboxylic acid, formic acid (HCOOH), was first obtained by the distillation of ants (Latin formica, meaning “ant”). The bites of some ants inject formic acid, and the stings of wasps and bees contain formic acid (as well as other poisonous materials).

    formic acid.jpg

    The next higher homolog is acetic acid, which is made by fermenting cider and honey in the presence of oxygen. This fermentation produces vinegar, a solution containing 4%–10% acetic acid, plus a number of other compounds that add to its flavor. Acetic acid is probably the most familiar weak acid used in educational and industrial chemistry laboratories.

    acetic acid.jpg

    Pure acetic acid solidifies at 16.6°C, only slightly below normal room temperature. In the poorly heated laboratories of the late 19th and early 20th centuries in northern North America and Europe, acetic acid often “froze” on the storage shelf. For that reason, pure acetic acid (sometimes called concentrated acetic acid) came to be known as glacial acetic acid, a name that survives to this day.

    The third homolog, propionic acid (CH3CH2COOH), is seldom encountered in everyday life. The fourth homolog, butyric acid (CH3CH2CH2COOH), is one of the most foul-smelling substances imaginable. It is found in rancid butter and is one of the ingredients of body odor. By recognizing extremely small amounts of this and other chemicals, bloodhounds are able to track fugitives. Models of the first four carboxylic acids are shown in Figure \(\PageIndex{2}\).

    Figure \(\PageIndex{2}\): Ball-and-Stick Models of Carboxylic Acids. Carboxylic acids feature a carbon atom doubly bonded to an oxygen atom and also joined to an OH group. The four acids illustrated here are formic acid (a), acetic acid (b), propionic acid (c), and butyric acid (d).

    The acid with the carboxyl group attached directly to a benzene ring is called benzoic acid (C6H5COOH).

    benzoic acid.jpg

    Many carboxylic acids are colorless liquids with disagreeable odors. The carboxylic acids with 5 to 10 carbon atoms all have “goaty” odors (explaining the odor of Limburger cheese). These acids are also produced by the action of skin bacteria on human sebum (skin oils), which accounts for the odor of poorly ventilated locker rooms. The acids with more than 10 carbon atoms are waxlike solids, and their odor diminishes with increasing molar mass and resultant decreasing volatility.

    Carboxylic acids exhibit strong hydrogen bonding between molecules. They therefore have high boiling points compared to other substances of comparable molar mass.

    The carboxyl group readily engages in hydrogen bonding with water molecules (Figure \(\PageIndex{1}\)). The acids with one to four carbon atoms are completely miscible with water. Solubility decreases as the carbon chain length increases because dipole forces become less important and dispersion forces become more predominant. Hexanoic acid [CH3(CH2)4COOH] is barely soluble in water (about 1.0 g/100 g of water). Palmitic acid [CH3(CH2)14COOH], with its large nonpolar hydrocarbon component, is essentially insoluble in water. The carboxylic acids generally are soluble in such organic solvents as ethanol, toluene, and diethyl ether.

    15.3.jpg
    Figure \(\PageIndex{1}\): Hydrogen Bonding between an Acetic Acid Molecule and Water Molecules. Carboxylic acids of low molar mass are quite soluble in water.

    Table 15.4.1 lists some physical properties for selected carboxylic acids. The first six are homologs. Notice that the boiling points increase with increasing molar mass, but the melting points show no regular pattern.

    Table \(\PageIndex{1}\): Physical Constants of Carboxylic Acids
    Condensed Structural Formula Name of Acid Melting Point (°C) Boiling Point (°C) Solubility (g/100 g of Water)
    HCOOH formic acid 8 100 miscible
    CH3COOH acetic acid 17 118 miscible
    CH3CH2COOH propion ic acid –22 141 miscible
    CH3(CH2)2COOH butyric acid –5 163 miscible
    CH3(CH2)3COOH valeric acid –35 187 5
    CH3(CH2)4COOH caproic acid –3 205 1.1
    C6H5COOH benzoic acid 122 249 0.29

     Esters

    Esters have the general formula RCOOR′, where R may be a hydrogen atom, an alkyl group, or an aryl group, and R′ may be an alkyl group or an aryl group but not a hydrogen atom. (If it were hydrogen atom, the compound would be a carboxylic acid.) Figure \(\PageIndex{1}\) shows models for two common esters.

    15.4.jpg
    Figure \(\PageIndex{1}\): The Structure of Esters. Esters feature a carbon-to-oxygen double bond that is also singly bonded to a second oxygen atom, which is then joined to an alkyl or an aryl group. The esters shown here are ethyl acetate (a) and methyl butyrate (b).

    Esters occur widely in nature. Unlike carboxylic acids, esters generally have pleasant odors and are often responsible for the characteristic fragrances of fruits and flowers. Once a flower or fruit has been chemically analyzed, flavor chemists can attempt to duplicate the natural odor or taste. Both natural and synthetic esters are used in perfumes and as flavoring agents.

    Fats and vegetable oils are esters of long-chain fatty acids and glycerol. Esters of phosphoric acid are of the utmost importance to life.

    Names of Esters

    Although esters are covalent compounds and salts are ionic, esters are named in a manner similar to that used for naming salts. The group name of the alkyl or aryl portion is given first and is followed by the name of the acid portion. In both common and International Union of Pure and Applied Chemistry (IUPAC) nomenclature, the -ic ending of the parent acid is replaced by the suffix -ate (Table \(\PageIndex{1}\)).

    Table \(\PageIndex{1}\): Nomenclature of Esters
    Condensed Structural Formula Common Name IUPAC Name
    HCOOCH3 methyl formate methyl methanoate
    CH3COOCH3 methyl acetate methyl ethanoate
    CH3COOCH2CH3 ethyl acetate ethyl ethanoate
    CH3CH2COOCH2CH3 ethyl propionate ethyl propanoate
    CH3CH2CH2COOCH(CH3)2 isopropyl butyrate isopropyl butanoate
    Table 15.3.jpg ethyl benzoate ethyl benzoate

    Example \(\PageIndex{1}\)

    Give the common and IUPAC names for each compound.

    1. Ex 5 1.jpg
    2. Ex 5 2.jpg

    Solution

    1. The alkyl group attached directly to the oxygen atom is a butyl group (in green).
      Ex 5 Ans 1.jpg






      The part of the molecule derived from the carboxylic acid (in red) has three carbon atoms. It is called propionate (common) or propanoate (IUPAC). The ester is therefore butyl propionate or butyl propanoate.

    2. An alkyl group (in green) is attached directly to the oxygen atom by its middle carbon atom; it is an isopropyl group. The part derived from the acid (that is, the benzene ring and the carbonyl group, in red) is benzoate. The ester is therefore isopropyl benzoate (both the common name and the IUPAC name).
      Ex 5 Ans 2.jpg

    Exercise \(\PageIndex{1}\)

    Give the common and IUPAC names for each compound.

    1. SB 1.jpg
    2. SB 2.jpg

    Example \(\PageIndex{2}\)

    Draw the structure for ethyl pentanoate.

    Solution

    Start with the portion from the acid. Draw the pentanoate (five carbon atoms) group first; keeping in mind that the last carbon atom is a part of the carboxyl group.

    Ex 6 1.jpg

    Then attach the ethyl group to the bond that ordinarily holds the hydrogen atom in the carboxyl group.

    Ex 6 2.jpg

    Exercise \(\PageIndex{2}\)

    Draw the structure for phenyl pentanoate.

    Preparation of Esters

    Some esters can be prepared by esterification, a reaction in which a carboxylic acid and an alcohol, heated in the presence of a mineral acid catalyst, form an ester and water:

    esterification.jpg

    The reaction is reversible. As a specific example of an esterification reaction, butyl acetate can be made from acetic acid and 1-butanol.

    butyl acetate.jpg

    A Closer Look: Condensation Polymers

    A commercially important esterification reaction is condensation polymerization, in which a reaction occurs between a dicarboxylic acid and a dihydric alcohol (diol), with the elimination of water. Such a reaction yields an ester that contains a free (unreacted) carboxyl group at one end and a free alcohol group at the other end. Further condensation reactions then occur, producing polyester polymers.

    The most important polyester, polyethylene terephthalate (PET), is made from terephthalic acid and ethylene glycol monomers:

    PET.jpg

    Polyester molecules make excellent fibers and are used in many fabrics. A knitted polyester tube, which is biologically inert, can be used in surgery to repair or replace diseased sections of blood vessels. PET is used to make bottles for soda pop and other beverages. It is also formed into films called Mylar. When magnetically coated, Mylar tape is used in audio- and videocassettes. Synthetic arteries can be made from PET, polytetrafluoroethylene, and other polymers.

    Summary

    Esters are made by the reaction of a carboxylic acid with an alcohol, a process that is called esterification.

    Concept Review Exercises

    1. From what carboxylic acid and what alcohol can the ester isopropyl nonanoate be made?
    2. From what carboxylic acid and what alcohol can the ester cyclobutyl butyrate be made?

    Answers

    1. nonanoic acid and isopropyl alcohol
    2. butyric acid and cyclobutyl alcohol

    Exercises

    1. Draw the structure for each compound.

      1. methyl acetate
      2. ethyl pentanoate
      3. phenyl acetate
      4. isopropyl propionate
    2. Name each compound with both the common name and the IUPAC name.

      1. Ex 3a.jpg
      2. Ex 3b.jpg

    3. Write the equation for the reaction of acetic acid with each compound.

    1. ethanol
    2. 1-butanol in the presence of a mineral acid catalyst

    Answers

      1. Ans 1a.jpg
      2. Ans 1b.jpg
      3. Ans 1c.jpg
      4. Ans 1d.jpg
      5. methyl formate; methyl methanoate
      1. ethyl propionate; ethyl propanoate  

       

    1a.jpg
    1. 1b.jpg

     

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