2.3: Representing Molecules
- Page ID
- 389543
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\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)- To understand the basic concept of electrostatic interaction
- To describe the basic difference between ionic and covalent bonds
- To be able to write the molecular formula of a molecule from the atoms in it
- To be able to identify the elements and number of atoms in a covalent molecule
- To interpret structure formulas, ball-and-stick models, perspective drawings, and condensed structural formulas
Atoms are the smallest, stable form of matter. Each unique type of atom is an element, like copper, sodium, or chlorine. Molecules are collections of atoms that behave as a single unit. The atoms do so by forming connections between each other in the forms of chemical bonds. Some molecules are made up of a single type of atom while other molecules are compounds, containing two or more different types of atoms.
The smallest, stable form of matter. Each atom is made of at least one proton, and may also have electrons and neutrons. The type of atom is defined by the number of protons it contains.
Two or more atoms connected together so strongly that they behave as a single particle.
A distinct substance that is composed of the atoms of two or more elements and always contains the same relative masses of those elements.
The atoms in molecules are held together by electrostatic interactions, the forces of attraction and repulsion between charged particles. Electrostatic attraction between oppositely charged species (positive and negative) results in a force that causes them to move toward each other, like the attraction between opposite poles of two magnets. In contrast, electrostatic repulsion between two species with the same charge (either both positive or both negative) results in a force that causes them to repel each other, as do the same poles of two magnets. In molecules, the attraction can be between either electrically charged particles which make up atoms, such as protons (nuclear charge) and electrons (electron charge), or between charged forms of atoms, called ions. Collectively, the attractive interactions between atoms are called chemical bonds if they occur between atoms within a single molecule. Atoms form chemical compounds when the attractive electrostatic interactions between them are stronger than the repulsive interactions.
An atom that a net positive or net negative electric charge.
A positively charged ion.
A negatively charged ion.
Chemical bonds are generally divided into two fundamentally different types: ionic bonds and covalent bonds. These will be discussed in more detail, including proper definitions, later. For our purposes now, we can state that a covalent bond is the name for bonding caused by the attraction between the proton in on atom and the electron in another atom. We will focus on covalent bonds because they are the bonds present in images when most people think of molecules. Covalent bonds are also the bond type in molecules consisting of the same element.
Covalent Molecules and Compounds
Just as an atom is the simplest unit that has the fundamental chemical properties of an element, a molecule is the simplest unit that has the fundamental chemical properties of a covalent compound. Some pure elements exist as covalent molecules. Hydrogen, nitrogen, oxygen, and the halogens occur naturally as the diatomic (“two atoms”) molecules H2, N2, O2, F2, Cl2, Br2, and I2 (part (a) in Figure \(\PageIndex{1}\)). Similarly, a few pure elements exist as polyatomic (“many atoms”) molecules, such as elemental phosphorus and sulfur, which occur as P4 and S8 (part (b) in Figure \(\PageIndex{1}\)).
Each covalent compound is represented by a molecular formula, which gives the atomic symbol for each component element, in a prescribed order, accompanied by a subscript indicating the number of atoms of that element in the molecule. The subscript is written only if the number of atoms is greater than 1. For example, water, with two hydrogen atoms and one oxygen atom per molecule, is written as \(H_2O\). Similarly, carbon dioxide, which contains one carbon atom and two oxygen atoms in each molecule, is written as \(CO_2\).
Covalent compounds that predominantly contain carbon and hydrogen are called organic compounds. The convention for representing the formulas of organic compounds is to write carbon first, followed by hydrogen and then any other elements in alphabetical order (e.g., CH4O is methyl alcohol, a fuel). Compounds that consist primarily of elements other than carbon and hydrogen are called inorganic compounds; they include both covalent and ionic compounds. In inorganic compounds, the component elements are listed beginning with the one farthest to the left in the periodic table, as in CO2 or SF6. Those in the same group are listed beginning with the lower element and working up, as in ClF. By convention, however, when an inorganic compound contains both hydrogen and an element from groups 13–15, hydrogen is usually listed last in the formula. Examples are ammonia (NH3) and silane (SiH4). Compounds such as water, whose compositions were established long before this convention was adopted, are always written with hydrogen first: Water is always written as H2O, not OH2. The conventions for inorganic acids, such as hydrochloric acid (HCl) and sulfuric acid (H2SO4), are described in Section 2.8.
For organic compounds: write C first, then H, and then the other elements in alphabetical order. For molecular inorganic compounds: start with the element at far left in the periodic table; list elements in same group beginning with the lower element and working up.
Write the molecular formula of each compound.
- The phosphorus-sulfur compound that is responsible for the ignition of so-called strike anywhere matches has 4 phosphorus atoms and 3 sulfur atoms per molecule.
- Ethyl alcohol, the alcohol of alcoholic beverages, has 1 oxygen atom, 2 carbon atoms, and 6 hydrogen atoms per molecule.
- Freon-11, once widely used in automobile air conditioners and implicated in damage to the ozone layer, has 1 carbon atom, 3 chlorine atoms, and 1 fluorine atom per molecule.
Given: identity of elements present and number of atoms of each
Asked for: molecular formula
Strategy:
- Identify the symbol for each element in the molecule. Then identify the substance as either an organic compound or an inorganic compound.
- If the substance is an organic compound, arrange the elements in order beginning with carbon and hydrogen and then list the other elements alphabetically. If it is an inorganic compound, list the elements beginning with the one farthest left in the periodic table. List elements in the same group starting with the lower element and working up.
- From the information given, add a subscript for each kind of atom to write the molecular formula.
Solution
a
- The molecule has 4 phosphorus atoms and 3 sulfur atoms. Because the compound does not contain mostly carbon and hydrogen, it is inorganic.
- Phosphorus is in group 15, and sulfur is in group 16. Because phosphorus is to the left of sulfur, it is written first.
- Writing the number of each kind of atom as a right-hand subscript gives P4S3 as the molecular formula.
b.
- Ethyl alcohol contains predominantly carbon and hydrogen, so it is an organic compound.
- The formula for an organic compound is written with the number of carbon atoms first, the number of hydrogen atoms next, and the other atoms in alphabetical order: CHO.
- Adding subscripts gives the molecular formula ]\(C_2H_6O\).
c
- Freon-11 contains carbon, chlorine, and fluorine. It can be viewed as either an inorganic compound or an organic compound (in which fluorine has replaced hydrogen). The formula for Freon-11 can therefore be written using either of the two conventions.
- According to the convention for inorganic compounds, carbon is written first because it is farther left in the periodic table. Fluorine and chlorine are in the same group, so they are listed beginning with the lower element and working up: CClF. Adding subscripts gives the molecular formula CCl3F.
- We obtain the same formula for Freon-11 using the convention for organic compounds. The number of carbon atoms is written first, followed by the number of hydrogen atoms (zero) and then the other elements in alphabetical order, also giving CCl3F.
Write the molecular formula for each compound.
- Nitrous oxide, also called “laughing gas,” has 2 nitrogen atoms and 1 oxygen atom per molecule. Nitrous oxide is used as a mild anesthetic for minor surgery and as the propellant in cans of whipped cream.
- Sucrose, also known as cane sugar, has 12 carbon atoms, 11 oxygen atoms, and 22 hydrogen atoms.
- Sulfur hexafluoride, a gas used to pressurize “unpressurized” tennis balls and as a coolant in nuclear reactors, has 6 fluorine atoms and 1 sulfur atom per molecule.
- Answer a
-
N2O
- Answer b
-
C12H22O11
- Answer c
-
SF6
Representations of Molecular Structures
Molecular formulas give only the elemental composition of molecules. In contrast, structural formulas show which atoms are bonded to one another and, in some cases, the approximate arrangement of the atoms in space. Knowing the structural formula of a compound enables chemists to create a three-dimensional model, which provides information about how that compound will behave physically and chemically.
The structural formula for H2 can be drawn as H–H and that for I2 as I–I, where the line indicates a single pair of shared electrons, a single bond. Two pairs of electrons are shared in a double bond, which is indicated by two lines—for example, O2 is O=O. Three electron pairs are shared in a triple bond, which is indicated by three lines—for example, N2 is N≡N (see Figure \(\PageIndex{2}\)). Carbon is unique in the extent to which it forms single, double, and triple bonds to itself and other elements. The number of bonds formed by an atom in its covalent compounds is not arbitrary. Hydrogen, oxygen, nitrogen, and carbon have very strong tendencies to form substances in which they have one, two, three, and four bonds to other atoms, respectively (Table \(\PageIndex{1}\)).
Atom | Number of Bonds |
---|---|
H (group 1) | 1 |
O (group 16) | 2 |
N (group 15) | 3 |
C (group 14) | 4 |
The structural formula for water can be drawn as follows:
Because the latter approximates the experimentally determined shape of the water molecule, it is more informative. Similarly, ammonia (NH3) and methane (CH4) are often written as planar molecules:
Figures \(\PageIndex{1}\), \(\PageIndex{2}\), and \(\PageIndex{3}\) illustrate different ways to represent the structures of molecules. It should be clear that there is no single “best” way to draw the structure of a molecule; the method used depends on which aspect of the structure should be emphasized and how much time and effort is required. Figure \(\PageIndex{4}\) shows some of the different ways to portray the structure of a slightly more complex molecule: methanol. These representations differ greatly in their information content. For example, the molecular formula for methanol (Figure \(\PageIndex{4a}\)) gives only the number of each kind of atom; writing methanol as CH4O tells nothing about its structure. In contrast, the structural formula (Figure \(\PageIndex{4b}\)) indicates how the atoms are connected, but it makes methanol look as if it is planar (which it is not). Both the ball-and-stick model (part (c) in Figure \(\PageIndex{4}\)) and the perspective drawing (Figure \(\PageIndex{4d}\)) show the three-dimensional structure of the molecule. The latter (also called a wedge-and-dash representation) is the easiest way to sketch the structure of a molecule in three dimensions. It shows which atoms are above and below the plane of the paper by using wedges and dashes, respectively; the central atom is always assumed to be in the plane of the paper. The space-filling model (part (e) in Figure \(\PageIndex{4}\)) illustrates the approximate relative sizes of the atoms in the molecule, but it does not show the bonds between the atoms. In addition, in a space-filling model, atoms at the “front” of the molecule may obscure atoms at the “back.”
Although a structural formula, a ball-and-stick model, a perspective drawing, and a space-filling model provide a significant amount of information about the structure of a molecule, each requires time and effort. Consequently, chemists often use a condensed structural formula (part (f) in Figure \(\PageIndex{4}\)), which omits the lines representing bonds between atoms and simply lists the atoms bonded to a given atom next to it. Multiple groups attached to the same atom are shown in parentheses, followed by a subscript that indicates the number of such groups. For example, the condensed structural formula for methanol is CH3OH, which indicates that the molecule contains a CH3 unit that looks like a fragment of methane (CH4). Methanol can therefore be viewed either as a methane molecule in which one hydrogen atom has been replaced by an –OH group or as a water molecule in which one hydrogen atom has been replaced by a –CH3 fragment. Because of their ease of use and information content, we use condensed structural formulas for molecules throughout this text. Ball-and-stick models are used when needed to illustrate the three-dimensional structure of molecules, and space-filling models are used only when it is necessary to visualize the relative sizes of atoms or molecules to understand an important point.
Ions are represented in molecular formulas, structural formulas, perspective drawings, and condensed structural formulas with the charge of the atom as a superscript.
Write the molecular formula for each compound. The condensed structural formula is given.
- Sulfur monochloride (also called disulfur dichloride) is a vile-smelling, corrosive yellow liquid used in the production of synthetic rubber. Its condensed structural formula is ClSSCl.
- Ethylene glycol is the major ingredient in antifreeze. Its condensed structural formula is HOCH2CH2OH.
- Trimethylamine is one of the substances responsible for the smell of spoiled fish. Its condensed structural formula is (CH3)3N.
Given: condensed structural formula
Asked for: molecular formula
Strategy:
- Identify every element in the condensed structural formula and then determine whether the compound is organic or inorganic.
- As appropriate, use either organic or inorganic convention to list the elements. Then add appropriate subscripts to indicate the number of atoms of each element present in the molecular formula.
Solution:
The molecular formula lists the elements in the molecule and the number of atoms of each.
- A Each molecule of sulfur monochloride has two sulfur atoms and two chlorine atoms. Because it does not contain mostly carbon and hydrogen, it is an inorganic compound. B Sulfur lies to the left of chlorine in the periodic table, so it is written first in the formula. Adding subscripts gives the molecular formula S2Cl2.
- A Counting the atoms in ethylene glycol, we get six hydrogen atoms, two carbon atoms, and two oxygen atoms per molecule. The compound consists mostly of carbon and hydrogen atoms, so it is organic. B As with all organic compounds, C and H are written first in the molecular formula. Adding appropriate subscripts gives the molecular formula C2H6O2.
- A The condensed structural formula shows that trimethylamine contains three CH3 units, so we have one nitrogen atom, three carbon atoms, and nine hydrogen atoms per molecule. Because trimethylamine contains mostly carbon and hydrogen, it is an organic compound. B According to the convention for organic compounds, C and H are written first, giving the molecular formula C3H9N.
Write the molecular formula for each molecule.
- Chloroform, which was one of the first anesthetics and was used in many cough syrups until recently, contains one carbon atom, one hydrogen atom, and three chlorine atoms. Its condensed structural formula is \(\ce{CHCl3}\).
- Hydrazine is used as a propellant in the attitude jets of the space shuttle. Its condensed structural formula is \(\ce{H2NNH2}\).
- Putrescine is a pungent-smelling compound first isolated from extracts of rotting meat. Its condensed structural formula is H2NCH2CH2CH2CH2NH2. This is often written as \(\ce{H2N(CH2)4NH2}\) to indicate that there are four CH2 fragments linked together.
- Answer a
-
CHCl3
- Answer b
-
N2H4
- Answer c
-
C4H12N2
Summary
There are two fundamentally different kinds of chemical bonds (covalent and ionic) that cause substances to have very different properties. The atoms in chemical compounds are held together by attractive electrostatic interactions known as chemical bonds. The molecular formula of a covalent compound gives the types and numbers of atoms present. Compounds that contain predominantly carbon and hydrogen are called organic compounds, whereas compounds that consist primarily of elements other than carbon and hydrogen are inorganic compounds. Diatomic molecules contain two atoms, and polyatomic molecules contain more than two. A structural formula indicates the composition and approximate structure and shape of a molecule. Covalent molecular compounds, in contrast, consist of discrete molecules held together by weak intermolecular forces and can be gases, liquids, or solids at room temperature and pressure.