Adapted from LibreTexts: Organic Chemistry With a Biological Emphasis by Tim Soderberg (University of Minnesota, Morris) 1.2: Functional Groups and Organic nomenclature

Functional groups in organic compounds

Functional groups are structural units within organic compounds that are defined by specific bonding arrangements between specific atoms.  The structure of capsaicin (Figure 1) incorporates several functional groups, labeled in the figure below and explained throughout this section. 

Figure 1. Structure of capsaicin with labeled functional groups.

As we progress in our study of organic chemistry, it will become extremely important to be able to quickly recognize the most common functional groups, because they are the key structural elements that define how organic molecules react. For now, we will only worry about drawing and recognizing each functional group, as depicted by Lewis and line structures. 

The ‘default’ in organic chemistry (essentially, the lack of any functional groups) is given the term alkane, characterized by single bonds between carbon and carbon, or between carbon and hydrogen.  Methane, CH₄, is the natural gas you may burn in your furnace.  Octane, C₈H₁₈, is a component of gasoline.

Alkenes (sometimes called olefins) have carbon-carbon double bonds, and alkynes have carbon-carbon triple bonds.  Ethene, the simplest alkene example, is a gas that serves as a cellular signal in fruits to stimulate ripening.  If you want bananas to ripen quickly, put them in a paper bag along with an apple – the apple emits ethene gas, setting off the ripening process in the bananas. Ethyne, commonly called acetylene, is used as a fuel in welding blow torches.

Alkenes and alkynes

The bonding nature in alkenes is trigonal planar and in alkynes is linear.  Furthermore, many alkenes can take two geometric forms: cis or trans. The cis and trans forms of a given alkene are different molecules with different physical properties because there is a very high energy barrier to rotation about a double bond. In the example below, the difference between cis and trans alkenes is readily apparent. 

Alkanes, alkenes, and alkynes are all classified as hydrocarbons, because they are composed solely of carbon and hydrogen atoms. Alkanes are said to be saturated hydrocarbons, because the carbons are bonded to the maximum possible number of hydrogens  – in other words, they are saturated with hydrogen atoms.  The double and triple-bonded carbons in alkenes and alkynes have fewer hydrogen atoms bonded to them – they are thus referred to as unsaturated hydrocarbons.  Hydrogen can be added to double and triple bonds, in a type of reaction called ‘hydrogenation,’ which will be discussed in a later chapter.

The aromatic group is exemplified by benzene (which used to be a commonly used solvent in the organic lab, but was shown to be carcinogenic later), and naphthalene, a compound with a distinctive ‘mothball’ smell. Aromatic groups are planar (flat) ring structures and are widespread in nature.  

When the carbon of an alkane is bonded to one or more halogens, the group is referred to as a alkyl halide or haloalkane.  Chloroform is a useful solvent in the laboratory and was one of the earlier anesthetics used in surgery. Chlorodifluoromethane was used as a refrigerant and a propellant in aerosol sprays until the late twentieth century; but its use was discontinued after it was found to have harmful effects on the ozone layer. Bromoethane is a simple alkyl halide often used in organic synthesis. Alkyl halides groups are quite rare in biomolecules.

Haloalkanes

In the alcohol functional group, a single-bonded carbon is bonded to an OH group (the OH group, by itself, is referred to as a hydroxyl) not to be confused with the hydroxide polyatomic ion, OH^–. Except for methanol, all alcohols can be classified as primary, secondary, or tertiary.  In a primary alcohol, the carbon bonded to the hydroxyl group is also bonded to only one other carbon.  In a secondary alcohol and tertiary alcohol, the carbon is bonded to two or three other carbons, respectively. When the hydroxyl group is directly attached to an aromatic ring, the resulting group is called a phenol. The sulfur analog of an alcohol is called a thiol (from the Greek thio, for sulfur).

 

Alcohols, phenols, and thiols

Note that the definition of a phenol states that the hydroxyl oxygen must be directly attached to one of the carbons of the aromatic ring. The compound below, therefore, is not a phenol – it is a primary alcohol. 

The distinction is important, as there is a significant difference in the reactivity of alcohols and phenols.

In an ether functional group, a central oxygen is bonded to two carbons. Below is the structure of diethyl ether, a common laboratory solvent and also one of the first compounds to be used as an anesthetic during operations. The sulfur analog of an ether is called a thioether or sulfide.

Amines are characterized by nitrogen atoms with single bonds to hydrogen and carbon. Just as there are primary, secondary and tertiary alcohols, there are primary, secondary and tertiary amines. Ammonia is a special case with no carbon atoms, only hydrogen.

One of the most important properties of amines is that they are basic and are readily protonated to form ammonium cations. In the case where a nitrogen has four bonds to carbon (which is somewhat unusual in biomolecules), it is called a quaternary ammonium ion.

Phosphate and its derivative functional groups are ubiquitous in biomolecules.  A phosphate linked to a single organic group is called a phosphate ester; when it has links to two organic groups it is called a phosphate diester.  A linkage between two phosphates creates a phosphate anhydride. 

Organic phosphates

There are a number of functional groups that contain a carbon-oxygen double bond, which is commonly referred to as a carbonyl. Ketones and aldehydes are two closely related carbonyl-based functional groups that react in very similar ways.  In a ketone, the carbon atom of a carbonyl is bonded to two other carbons.  In an aldehyde, the carbonyl carbon is bonded on one side to a hydrogen, and on the other side to a carbon.  The exception to this definition is formaldehyde, in which the carbonyl carbon has bonds to two hydrogens.

A group with a carbon-nitrogen double bond is called an imine, or sometimes a Schiff base.

When a carbonyl carbon is bonded on one side to a carbon (or hydrogen) and on the other side to an oxygen, nitrogen, or sulfur, the functional group is considered to be one of the ‘carboxylic acid derivatives’, a designation that describes a set of related functional groups.  The eponymous member of this family is the carboxylic acid functional group, in which the carbonyl is bonded to a hydroxyl group.   The conjugate base of a carboxylic acid is a carboxylate.  Other derivatives are carboxylic esters (usually just called ‘esters’) and amides, to name a few.  These carboxylic acid derivatives are very common in biological molecules and metabolic pathways.

The hormone testosterone, the amino acid phenylalanine, and the glycolysis metabolite dihydroxyacetone phosphate all contain multiple functional groups, as labeled below.

While not in any way a complete list, this section has covered most of the important functional groups that we will encounter in biological organic chemistry. 

The table here summarizes the structures discussed in this chapter: