7.5: Hydrocarbons

Learning Objectives

By the end of this section, you will be able to:

• Explain the importance of hydrocarbons and the reason for their diversity
• Name saturated and unsaturated hydrocarbons, and molecules derived from them
• Describe the reactions characteristic of saturated and unsaturated hydrocarbons
• Identify structural and geometric isomers of hydrocarbons

The largest database¹ of organic compounds lists about 10 million substances, which include compounds originating from living organisms and those synthesized by chemists. The number of potential organic compounds has been estimated² at 10⁶⁰—an astronomically high number. The existence of so many organic molecules is a consequence of the ability of carbon atoms to form up to four strong bonds to other carbon atoms, resulting in chains and rings of many different sizes, shapes, and complexities.

The simplest organic compounds contain only the elements carbon and hydrogen, and are called hydrocarbons. Even though they are composed of only two types of atoms, there is a wide variety of hydrocarbons because they may consist of varying lengths of chains, branched chains, and rings of carbon atoms, or combinations of these structures. In addition, hydrocarbons may differ in the types of carbon-carbon bonds present in their molecules. Many hydrocarbons are found in plants, animals, and their fossils; other hydrocarbons have been prepared in the laboratory. We use hydrocarbons every day, mainly as fuels, such as natural gas, acetylene, propane, butane, and the principal components of gasoline, diesel fuel, and heating oil. The familiar plastics polyethylene, polypropylene, and polystyrene are also hydrocarbons. We can distinguish several types of hydrocarbons by differences in the bonding between carbon atoms. This leads to differences in geometries and in the hybridization of the carbon orbitals.

Alkanes

Alkanes, or saturated hydrocarbons, contain only single covalent bonds between carbon atoms. Each of the carbon atoms in an alkane has sp³ hybrid orbitals and is bonded to four other atoms, each of which is either carbon or hydrogen. The Lewis structures and models of methane, ethane, and pentane are illustrated in Figure \(\PageIndex{1}\). Carbon chains are usually drawn as straight lines in Lewis structures, but one has to remember that Lewis structures are not intended to indicate the geometry of molecules. Notice that the carbon atoms in the structural models (the ball-and-stick and space-filling models) of the pentane molecule do not lie in a straight line. Because of the sp³ hybridization, the bond angles in carbon chains are close to 109.5°, giving such chains in an alkane a zigzag shape.

The structures of alkanes and other organic molecules may also be represented in a less detailed manner by condensed structural formulas (or simply, condensed formulas). Instead of the usual format for chemical formulas in which each element symbol appears just once, a condensed formula is written to suggest the bonding in the molecule. These formulas have the appearance of a Lewis structure from which most or all of the bond symbols have been removed. Condensed structural formulas for ethane and pentane are shown at the bottom of Figure \(\PageIndex{1}\): , and several additional examples are provided in the exercises at the end of this chapter.

Figure \(\PageIndex{1}\): Pictured are the Lewis structures, ball-and-stick models, and space-filling models for molecules of methane, ethane, and pentane.

A common method used by organic chemists to simplify the drawings of larger molecules is to use a skeletal structure (also called a line-angle structure). In this type of structure, carbon atoms are not symbolized with a C, but represented by each end of a line or bend in a line. Hydrogen atoms are not drawn if they are attached to a carbon. Other atoms besides carbon and hydrogen are represented by their elemental symbols. Figure \(\PageIndex{2}\): shows three different ways to draw the same structure.

Figure \(\PageIndex{2}\): The same structure can be represented three different ways: an expanded formula, a condensed formula, and a skeletal structure.

Example \(\PageIndex{1}\): Drawing Skeletal Structures

Draw the skeletal structures for these two molecules:

Solution

Each carbon atom is converted into the end of a line or the place where lines intersect. All hydrogen atoms attached to the carbon atoms are left out of the structure (although we still need to recognize they are there):

Exercise \(\PageIndex{1}\)

Draw the skeletal structures for these two molecules:

Answer

Example \(\PageIndex{2}\): Interpreting Skeletal Structures

Identify the chemical formula of the molecule represented here:

Solution

There are eight places where lines intersect or end, meaning that there are eight carbon atoms in the molecule. Since we know that carbon atoms tend to make four bonds, each carbon atom will have the number of hydrogen atoms that are required for four bonds. This compound contains 16 hydrogen atoms for a molecular formula of C₈H₁₆.

Location of the hydrogen atoms:

Exercise \(\PageIndex{1}\)

Identify the chemical formula of the molecule represented here:

Answer

C₉H₂₀

All alkanes are composed of carbon and hydrogen atoms, and have similar bonds, structures, and formulas; noncyclic alkanes all have a formula of C_nH_2n+2. The number of carbon atoms present in an alkane has no limit. Greater numbers of atoms in the molecules will lead to stronger intermolecular attractions (dispersion forces) and correspondingly different physical properties of the molecules. Properties such as melting point and boiling point (Table 20.1) usually change smoothly and predictably as the number of carbon and hydrogen atoms in the molecules change.

Table 20.1: Properties of Some Alkanes³

Alkane	Molecular Formula	Melting Point (°C)	Boiling Point (°C)	Phase at STP^4	Number of Structural Isomers
methane	CH4	–182.5	–161.5	gas	1
ethane	C2H6	–183.3	–88.6	gas	1
propane	C3H8	–187.7	–42.1	gas	1
butane	C4H10	–138.3	–0.5	gas	2
pentane	C5H12	–129.7	36.1	liquid	3
hexane	C6H14	–95.3	68.7	liquid	5
heptane	C7H16	–90.6	98.4	liquid	9
octane	C8H18	–56.8	125.7	liquid	18
nonane	C9H20	–53.6	150.8	liquid	35
decane	C10H22	–29.7	174.0	liquid	75
tetradecane	C14H30	5.9	253.5	solid	1858
octadecane	C18H38	28.2	316.1	solid	60,523

Hydrocarbons with the same formula, including alkanes, can have different structures. For example, two alkanes have the formula C₄H₁₀: They are called n-butane and 2-methylpropane (or isobutane), and have the following Lewis structures:

The compounds n-butane and 2-methylpropane are structural isomers (the term constitutional isomers is also commonly used). Constitutional isomers have the same molecular formula but different spatial arrangements of the atoms in their molecules. The n-butane molecule contains an unbranched chain, meaning that no carbon atom is bonded to more than two other carbon atoms. We use the term normal, or the prefix n, to refer to a chain of carbon atoms without branching. The compound 2–methylpropane has a branched chain (the carbon atom in the center of the Lewis structure is bonded to three other carbon atoms)

Identifying isomers from Lewis structures is not as easy as it looks. Lewis structures that look different may actually represent the same isomers. For example, the three structures in Figure \(\PageIndex{3}\): all represent the same molecule, n-butane, and hence are not different isomers. They are identical because each contains an unbranched chain of four carbon atoms.

Figure \(\PageIndex{3}\): These three representations of the structure of n-butane are not isomers because they all contain the same arrangement of atoms and bonds.

The Basics of Organic Nomenclature: Naming Alkanes

The International Union of Pure and Applied Chemistry (IUPAC) has devised a system of nomenclature that begins with the names of the alkanes and can be adjusted from there to account for more complicated structures. The nomenclature for alkanes is based on two rules:

1. To name an alkane, first identify the longest chain of carbon atoms in its structure. A two-carbon chain is called ethane; a three-carbon chain, propane; and a four-carbon chain, butane. Longer chains are named as follows: pentane (five-carbon chain), hexane (6), heptane (7), octane (8), nonane (9), and decane (10). These prefixes can be seen in the names of the alkanes described in Table 20.1.
2. Add prefixes to the name of the longest chain to indicate the positions and names of substituents. Substituents are branches or functional groups that replace hydrogen atoms on a chain. The position of a substituent or branch is identified by the number of the carbon atom it is bonded to in the chain. We number the carbon atoms in the chain by counting from the end of the chain nearest the substituents. Multiple substituents are named individually and placed in alphabetical order at the front of the name.

When more than one substituent is present, either on the same carbon atom or on different carbon atoms, the substituents are listed alphabetically. Because the carbon atom numbering begins at the end closest to a substituent, the longest chain of carbon atoms is numbered in such a way as to produce the lowest number for the substituents. The ending -o replaces -ide at the end of the name of an electronegative substituent (in ionic compounds, the negatively charged ion ends with -ide like chloride; in organic compounds, such atoms are treated as substituents and the -o ending is used). The number of substituents of the same type is indicated by the prefixes di- (two), tri- (three), tetra- (four), and so on (for example, difluoro- indicates two fluoride substituents).

Example \(\PageIndex{3}\): Naming Halogen-substituted Alkanes

Name the molecule whose structure is shown here:

Solution

The four-carbon chain is numbered from the end with the chlorine atom. This puts the substituents on positions 1 and 2 (numbering from the other end would put the substituents on positions 3 and 4). Four carbon atoms means that the base name of this compound will be butane. The bromine at position 2 will be described by adding 2-bromo-; this will come at the beginning of the name, since bromo- comes before chloro- alphabetically. The chlorine at position 1 will be described by adding 1-chloro-, resulting in the name of the molecule being 2-bromo-1-chlorobutane.

Exercise \(\PageIndex{1}\)

Name the following molecule:

Answer

3,3-dibromo-2-iodopentane

We call a substituent that contains one less hydrogen than the corresponding alkane an alkyl group. The name of an alkyl group is obtained by dropping the suffix -ane of the alkane name and adding -yl:

The open bonds in the methyl and ethyl groups indicate that these alkyl groups are bonded to another atom.

Example \(\PageIndex{4}\): Naming Substituted Alkanes

Name the molecule whose structure is shown here:

Solution

The longest carbon chain runs horizontally across the page and contains six carbon atoms (this makes the base of the name hexane, but we will also need to incorporate the name of the branch). In this case, we want to number from right to left (as shown by the blue numbers) so the branch is connected to carbon 3 (imagine the numbers from left to right—this would put the branch on carbon 4, violating our rules). The branch attached to position 3 of our chain contains two carbon atoms (numbered in red)—so we take our name for two carbons eth- and attach -yl at the end to signify we are describing a branch. Putting all the pieces together, this molecule is 3-ethylhexane.

Exercise \(\PageIndex{1}\)

Name the following molecule:

Answer

4-propyloctane

Some hydrocarbons can form more than one type of alkyl group when the hydrogen atoms that would be removed have different “environments” in the molecule. This diversity of possible alkyl groups can be identified in the following way: The four hydrogen atoms in a methane molecule are equivalent; they all have the same environment. They are equivalent because each is bonded to a carbon atom (the same carbon atom) that is bonded to three hydrogen atoms. (It may be easier to see the equivalency in the ball and stick models in Figure \(\PageIndex{1}\). Removal of any one of the four hydrogen atoms from methane forms a methyl group. Likewise, the six hydrogen atoms in ethane are equivalent (Figure \(\PageIndex{1}\)) and removing any one of these hydrogen atoms produces an ethyl group. Each of the six hydrogen atoms is bonded to a carbon atom that is bonded to two other hydrogen atoms and a carbon atom. However, in both propane and 2–methylpropane, there are hydrogen atoms in two different environments, distinguished by the adjacent atoms or groups of atoms:

Each of the six equivalent hydrogen atoms of the first type in propane and each of the nine equivalent hydrogen atoms of that type in 2-methylpropane (all shown in black) are bonded to a carbon atom that is bonded to only one other carbon atom. The two purple hydrogen atoms in propane are of a second type. They differ from the six hydrogen atoms of the first type in that they are bonded to a carbon atom bonded to two other carbon atoms. The green hydrogen atom in 2-methylpropane differs from the other nine hydrogen atoms in that molecule and from the purple hydrogen atoms in propane. The green hydrogen atom in 2-methylpropane is bonded to a carbon atom bonded to three other carbon atoms. Two different alkyl groups can be formed from each of these molecules, depending on which hydrogen atom is removed. The names and structures of these and several other alkyl groups are listed in Figure \(\PageIndex{4}\).

Figure \(\PageIndex{4}\): This listing gives the names and formulas for various alkyl groups formed by the removal of hydrogen atoms from different locations.

Note that alkyl groups do not exist as stable independent entities. They are always a part of some larger molecule. The location of an alkyl group on a hydrocarbon chain is indicated in the same way as any other substituent:

Alkanes are relatively stable molecules, but heat or light will activate reactions that involve the breaking of C–H or C–C single bonds. Combustion is one such reaction:

Alkanes burn in the presence of oxygen, a highly exothermic oxidation-reduction reaction that produces carbon dioxide and water. As a consequence, alkanes are excellent fuels. For example, methane, CH₄, is the principal component of natural gas. Butane, C₄H₁₀, used in camping stoves and lighters is an alkane. Gasoline is a liquid mixture of continuous- and branched-chain alkanes, each containing from five to nine carbon atoms, plus various additives to improve its performance as a fuel. Kerosene, diesel oil, and fuel oil are primarily mixtures of alkanes with higher molecular masses. The main source of these liquid alkane fuels is crude oil, a complex mixture that is separated by fractional distillation. Fractional distillation takes advantage of differences in the boiling points of the components of the mixture (see Figure \(\PageIndex{5}\)). You may recall that boiling point is a function of intermolecular interactions, which was discussed in the chapter on solutions and colloids.

Figure \(\PageIndex{5}\): In a column for the fractional distillation of crude oil, oil heated to about 425 °C in the furnace vaporizes when it enters the base of the tower. The vapors rise through bubble caps in a series of trays in the tower. As the vapors gradually cool, fractions of higher, then of lower, boiling points condense to liquids and are drawn off. (credit left: modification of work by Luigi Chiesa)

In a substitution reaction, another typical reaction of alkanes, one or more of the alkane’s hydrogen atoms is replaced with a different atom or group of atoms. No carbon-carbon bonds are broken in these reactions, and the hybridization of the carbon atoms does not change. For example, the reaction between ethane and molecular chlorine depicted here is a substitution reaction:

The C–Cl portion of the chloroethane molecule is an example of a functional group, the part or moiety of a molecule that imparts a specific chemical reactivity. The types of functional groups present in an organic molecule are major determinants of its chemical properties and are used as a means of classifying organic compounds as detailed in the remaining sections of this chapter.

Link to Learning

Want more practice naming alkanes? Watch this brief video tutorial to review the nomenclature process.

Alkenes

Organic compounds that contain one or more double or triple bonds between carbon atoms are described as unsaturated. You have likely heard of unsaturated fats. These are complex organic molecules with long chains of carbon atoms, which contain at least one double bond between carbon atoms. Unsaturated hydrocarbon molecules that contain one or more double bonds are called alkenes. Carbon atoms linked by a double bond are bound together by two bonds, one σ bond and one π bond. Double and triple bonds give rise to a different geometry around the carbon atom that participates in them, leading to important differences in molecular shape and properties. The differing geometries are responsible for the different properties of unsaturated versus saturated fats.

Ethene, C₂H₄, is the simplest alkene. Each carbon atom in ethene, commonly called ethylene, has a trigonal planar structure. The second member of the series is propene (propylene) (Figure \(\PageIndex{6}\)); the butene isomers follow in the series. Four carbon atoms in the chain of butene allows for the formation of isomers based on the position of the double bond, as well as a new form of isomerism.

Figure \(\PageIndex{6}\): Expanded structures, ball-and-stick structures, and space-filling models for the alkenes ethene, propene, and 1-butene are shown.

Ethylene (the common industrial name for ethene) is a basic raw material in the production of polyethylene and other important compounds. Over 135 million tons of ethylene were produced worldwide in 2010 for use in the polymer, petrochemical, and plastic industries. Ethylene is produced industrially in a process called cracking, in which the long hydrocarbon chains in a petroleum mixture are broken into smaller molecules.

Chemistry in Everyday Life: Recycling Plastics

Polymers (from Greek words poly meaning “many” and mer meaning “parts”) are large molecules made up of repeating units, referred to as monomers. Polymers can be natural (starch is a polymer of sugar residues and proteins are polymers of amino acids) or synthetic [like polyethylene, polyvinyl chloride (PVC), and polystyrene]. The variety of structures of polymers translates into a broad range of properties and uses that make them integral parts of our everyday lives. Adding functional groups to the structure of a polymer can result in significantly different properties (see the discussion about Kevlar later in this chapter).

An example of a polymerization reaction is shown in Figure \(\PageIndex{7}\). The monomer ethylene (C₂H₄) is a gas at room temperature, but when polymerized, using a transition metal catalyst, it is transformed into a solid material made up of long chains of –CH₂– units called polyethylene. Polyethylene is a commodity plastic used primarily for packaging (bags and films).

Figure \(\PageIndex{7}\): The reaction for the polymerization of ethylene to polyethylene is shown.

Polyethylene is a member of one subset of synthetic polymers classified as plastics. Plastics are synthetic organic solids that can be molded; they are typically organic polymers with high molecular masses. Most of the monomers that go into common plastics (ethylene, propylene, vinyl chloride, styrene, and ethylene terephthalate) are derived from petrochemicals and are not very biodegradable, making them candidate materials for recycling. Recycling plastics helps minimize the need for using more of the petrochemical supplies and also minimizes the environmental damage caused by throwing away these nonbiodegradable materials.

Plastic recycling is the process of recovering waste, scrap, or used plastics, and reprocessing the material into useful products. For example, polyethylene terephthalate (soft drink bottles) can be melted down and used for plastic furniture, in carpets, or for other applications. Other plastics, like polyethylene (bags) and polypropylene (cups, plastic food containers), can be recycled or reprocessed to be used again. Many areas of the country have recycling programs that focus on one or more of the commodity plastics that have been assigned a recycling code (see Figure \(\PageIndex{8}\)). These operations have been in effect since the 1970s and have made the production of some plastics among the most efficient industrial operations today.

Figure \(\PageIndex{8}\): Each type of recyclable plastic is imprinted with a code for easy identification.

The name of an alkene is derived from the name of the alkane with the same number of carbon atoms. The presence of the double bond is signified by replacing the suffix -ane with the suffix -ene. The location of the double bond is identified by naming the smaller of the numbers of the carbon atoms participating in the double bond:

Isomers of Alkenes

Molecules of 1-butene and 2-butene are structural isomers; the arrangement of the atoms in these two molecules differs. As an example of arrangement differences, the first carbon atom in 1-butene is bonded to two hydrogen atoms; the first carbon atom in 2-butene is bonded to three hydrogen atoms.

The compound 2-butene and some other alkenes also form a second type of isomer called a geometric isomer. In a set of geometric isomers, the same types of atoms are attached to each other in the same order, but the geometries of the two molecules differ. Geometric isomers of alkenes differ in the orientation of the groups on either side of a bond.

Carbon atoms are free to rotate around a single bond but not around a double bond; a double bond is rigid. This makes it possible to have two isomers of 2-butene, one with both methyl groups on the same side of the double bond and one with the methyl groups on opposite sides. When structures of butene are drawn with 120° bond angles around the sp²-hybridized carbon atoms participating in the double bond, the isomers are apparent. The 2-butene isomer in which the two methyl groups are on the same side is called a cis-isomer; the one in which the two methyl groups are on opposite sides is called a trans-isomer (Figure \(\PageIndex{9}\)). The different geometries produce different physical properties, such as boiling point, that may make separation of the isomers possible:

Figure \(\PageIndex{9}\): These molecular models show the structural and geometric isomers of butene.

Alkenes are much more reactive than alkanes because the moiety is a reactive functional group. A π bond, being a weaker bond, is disrupted much more easily than a σ bond. Thus, alkenes undergo a characteristic reaction in which the π bond is broken and replaced by two σ bonds. This reaction is called an addition reaction. The hybridization of the carbon atoms in the double bond in an alkene changes from sp² to sp³ during an addition reaction. For example, halogens add to the double bond in an alkene instead of replacing hydrogen, as occurs in an alkane:

Example \(\PageIndex{5}\): Alkene Reactivity and Naming

Provide the IUPAC names for the reactant and product of the halogenation reaction shown here:

Solution

The reactant is a five-carbon chain that contains a carbon-carbon double bond, so the base name will be pentene. We begin counting at the end of the chain closest to the double bond—in this case, from the left—the double bond spans carbons 2 and 3, so the name becomes 2-pentene. Since there are two carbon-containing groups attached to the two carbon atoms in the double bond—and they are on the same side of the double bond—this molecule is the cis-isomer, making the name of the starting alkene cis-2-pentene. The product of the halogenation reaction will have two chlorine atoms attached to the carbon atoms that were a part of the carbon-carbon double bond:

This molecule is now a substituted alkane and will be named as such. The base of the name will be pentane. We will count from the end that numbers the carbon atoms where the chlorine atoms are attached as 2 and 3, making the name of the product 2,3-dichloropentane.

Exercise \(\PageIndex{1}\)

Provide names for the reactant and product of the reaction shown:

Answer

reactant: cis-3-hexene product: 3,4-dichlorohexane

Alkynes

Hydrocarbon molecules with one or more triple bonds are called alkynes; they make up another series of unsaturated hydrocarbons. Two carbon atoms joined by a triple bond are bound together by one σ bond and two π bonds. The sp-hybridized carbons involved in the triple bond have bond angles of 180°, giving these types of bonds a linear, rod-like shape.

The simplest member of the alkyne series is ethyne, C₂H₂, commonly called acetylene. The Lewis structure for ethyne, a linear molecule, is:

The IUPAC nomenclature for alkynes is similar to that for alkenes except that the suffix -yne is used to indicate a triple bond in the chain. For example, is called 1-butyne.

Example \(\PageIndex{6}\): Structure of Alkynes

Describe the geometry and hybridization of the carbon atoms in the following molecule:

Solution

Carbon atoms 1 and 4 have four single bonds and are thus tetrahedral with sp³ hybridization. Carbon atoms 2 and 3 are involved in the triple bond, so they have linear geometries and would be classified as sp hybrids.

Exercise \(\PageIndex{1}\)

Identify the hybridization and bond angles at the carbon atoms in the molecule shown:

Answer

carbon 1: sp, 180°; carbon 2: sp, 180°; carbon 3: sp², 120°; carbon 4: sp², 120°; carbon 5: sp³, 109.5°

Chemically, the alkynes are similar to the alkenes. Since the functional group has two π bonds, alkynes typically react even more readily, and react with twice as much reagent in addition reactions. The reaction of acetylene with bromine is a typical example:

Acetylene and the other alkynes also burn readily. An acetylene torch takes advantage of the high heat of combustion for acetylene.

Aromatic Hydrocarbons

Benzene, C₆H₆, is the simplest member of a large family of hydrocarbons, called aromatic hydrocarbons. These compounds contain ring structures and exhibit bonding that must be described using the resonance hybrid concept of valence bond theory or the delocalization concept of molecular orbital theory. (To review these concepts, refer to the earlier chapters on chemical bonding). The resonance structures for benzene, C₆H₆, are:

Valence bond theory describes the benzene molecule and other planar aromatic hydrocarbon molecules as hexagonal rings of sp²-hybridized carbon atoms with the unhybridized p orbital of each carbon atom perpendicular to the plane of the ring. Three valence electrons in the sp² hybrid orbitals of each carbon atom and the valence electron of each hydrogen atom form the framework of σ bonds in the benzene molecule. The fourth valence electron of each carbon atom is shared with an adjacent carbon atom in their unhybridized p orbitals to yield the π bonds. Benzene does not, however, exhibit the characteristics typical of an alkene. Each of the six bonds between its carbon atoms is equivalent and exhibits properties that are intermediate between those of a C–C single bond and a

Figure \(\PageIndex{10}\): This condensed formula shows the unique bonding structure of benzene.

There are many derivatives of benzene. The hydrogen atoms can be replaced by many different substituents. Aromatic compounds more readily undergo substitution reactions than addition reactions; replacement of one of the hydrogen atoms with another substituent will leave the delocalized double bonds intact. The following are typical examples of substituted benzene derivatives:

Toluene and xylene are important solvents and raw materials in the chemical industry. Styrene is used to produce the polymer polystyrene.

Example \(\PageIndex{7}\): Structure of Aromatic Hydrocarbons

One possible isomer created by a substitution reaction that replaces a hydrogen atom attached to the aromatic ring of toluene with a chlorine atom is shown here. Draw two other possible isomers in which the chlorine atom replaces a different hydrogen atom attached to the aromatic ring:

Solution

Since the six-carbon ring with alternating double bonds is necessary for the molecule to be classified as aromatic, appropriate isomers can be produced only by changing the positions of the chloro-substituent relative to the methyl-substituent:

Exercise \(\PageIndex{1}\)

Draw three isomers of a six-membered aromatic ring compound substituted with two bromines.

Answer

Footnotes

• 1This is the Beilstein database, now available through the Reaxys site (www.elsevier.com/online-tools/reaxys).
• 2Peplow, Mark. “Organic Synthesis: The Robo-Chemist,” Nature 512 (2014): 20–2.
• 3Physical properties for C₄H₁₀ and heavier molecules are those of the normal isomer, n-butane, n-pentane, etc.
• 4STP indicates a temperature of 0 °C and a pressure of 1 atm.