Skip to main content
Chemistry LibreTexts

2.7: Covalent Bonding and Formula Writing

  • Page ID
    466583
  • \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)

    \( \newcommand{\dsum}{\displaystyle\sum\limits} \)

    \( \newcommand{\dint}{\displaystyle\int\limits} \)

    \( \newcommand{\dlim}{\displaystyle\lim\limits} \)

    \( \newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\)

    ( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\)

    \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)

    \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\)

    \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)

    \( \newcommand{\Span}{\mathrm{span}}\)

    \( \newcommand{\id}{\mathrm{id}}\)

    \( \newcommand{\Span}{\mathrm{span}}\)

    \( \newcommand{\kernel}{\mathrm{null}\,}\)

    \( \newcommand{\range}{\mathrm{range}\,}\)

    \( \newcommand{\RealPart}{\mathrm{Re}}\)

    \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)

    \( \newcommand{\Argument}{\mathrm{Arg}}\)

    \( \newcommand{\norm}[1]{\| #1 \|}\)

    \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)

    \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\AA}{\unicode[.8,0]{x212B}}\)

    \( \newcommand{\vectorA}[1]{\vec{#1}}      % arrow\)

    \( \newcommand{\vectorAt}[1]{\vec{\text{#1}}}      % arrow\)

    \( \newcommand{\vectorB}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \( \newcommand{\vectorC}[1]{\textbf{#1}} \)

    \( \newcommand{\vectorD}[1]{\overrightarrow{#1}} \)

    \( \newcommand{\vectorDt}[1]{\overrightarrow{\text{#1}}} \)

    \( \newcommand{\vectE}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{\mathbf {#1}}}} \)

    \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \(\newcommand{\longvect}{\overrightarrow}\)

    \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)

    \(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)
    Learning Objectives
    • Describe the properties of a covalent bond
    • Use Lewis structures to represent covalent bonding in molecular substances
    • Use a Lewis structure to determine how many single, double, and triple bonds are present in a molecule
    • Write the formulas and names for binary covalent compounds

    Electron Sharing

    Previously, we discussed ionic bonding where electrons can be transferred from one atom to another so that both atoms have an energy-stable outer electron shell. Because most filled electron shells have eight electrons in them, chemists called this tendency the octet rule. However, there is another way an atom can achieve a full valence shell: atoms can share electrons. This type of bonding is called a covalent bond. Two combinations of atoms can produce this type of bonding: nonmetal with nonmetal or metalloid with nonmetal. In this class, we will not discuss the option of metallic bonding which is a form of covalent bonding.

    Close‑up sequence of three red disposable cup sleeves stacked vertically, each printed with the word “SHARE” in bold white letters. The images progress from sharp focus at the top to increasingly blurred text at the bottom, visually demonstrating the effect of changing focus or depth of field.
    Figure \(\PageIndex{1}\): Sharing is caring, especially for atoms that participate in covalent bonding. (CC BY-2.0; Carlos Maya).

    This concept can be illustrated by using two hydrogen atoms, each of which has a single electron in its valence shell. (For small atoms such as hydrogen atoms, the valence shell will be the first shell, which holds a maximum of only two electrons.) We can represent the two individual hydrogen atoms as follows (the blue circle represents the single proton found in each atomic nucleus, the red circle represents the single electron found in its valence shell): 

    Two simplified atomic diagrams showing a single‑electron atom. In each diagram, a small blue dot at the center represents one proton in the nucleus, and a single red dot on the outer region represents one electron in the valence shell. The two images show the electron positioned at different locations around the nucleus, illustrating that the electron can occupy different positions while remaining in the same outer shell.

    In contrast, when two hydrogen atoms get close enough together to share their electrons, they can be represented as follows:

    Diagram illustrating a covalent bond between two atoms. Two overlapping circular regions represent the atoms, each with a central blue dot indicating a proton in the nucleus. In the overlapping region between the atoms, two red dots represent a shared pair of valence electrons, showing that the electrons are shared between both atoms to form a covalent bond.

    By sharing their valence electrons, both hydrogen atoms now have two electrons in their respective valence shells. Because each valence shell is now filled, this arrangement is more stable than when the two atoms are separate. The sharing of electrons between atoms is called a covalent bond, and the two electrons that join atoms in a covalent bond are called a bonding pair of electrons. A discrete group of atoms connected by covalent bonds is called a molecule — the smallest part of a compound that retains the chemical identity of that compound.

    Chemists frequently use Lewis structures to represent covalent bonding in molecular substances. For example, the Lewis dot structures of two separate hydrogen atoms are as follows:

    Two hydrogen atoms depicted by their Lewis dot symbol each with an H and a single dot

    The Lewis diagram of two hydrogen atoms sharing electrons looks like this:

    Lewis dot structure of two hydrogen atoms covalently bonded together, illustrated with two capital H's with two dots oriented vertical in between the two letters, indicating two valence electrons are being shared between the two atoms of hydrogen

    This depiction of molecules is simplified further by using a dash to represent a covalent bond. The Lewis structure of the hydrogen molecule is then represented as follows:

    Lewis structure of molecular hydrogen with two capital H's separated by a long dash, indicating two electrons are being shared in a covalent bond between the two atoms of hydrogen

    Remember that the dash, also referred to as a single bond, represents a pair of electrons.

    The bond in a hydrogen molecule, measured as the distance between the two nuclei, is about 7.4 × 10−11 m, or 74 picometers (pm; 1 pm = 1 × 10−12 m). This particular bond length represents a balance between several forces: the attraction between oppositely charged electrons and nuclei, the repulsion between two negatively charged electrons, and the repulsion between two positively charged nuclei. If the nuclei were closer together, they would repel each other more strongly; if the nuclei were farther apart, there would be less attraction between the positive and negative particles.

    Fluorine is another element whose atoms bond together in pairs to form diatomic (two-atom) molecules. Two separate fluorine atoms have the following electron dot diagrams:

    Lewis dot structures of two atoms of fluorine, each with seven dots oriented around them indicating 7 valence electrons

    Each fluorine atom contributes one valence electron, making a single bond and giving each atom a complete valence shell, which fulfills the octet rule:

    Lewis dot structure of two fluorine atoms covalently bonded together, sharing two valence electrons.

    The circles show that each fluorine atom has eight electrons around it (a full octet). As with hydrogen, we can represent the Lewis structure of the fluorine molecule with a dash in place of the bonding electrons:

    Lewis structure of molecular fluorine with each fluorine atom having 3 pairs of dots connected together by a single dash representing the two electrons shared between the two atoms of fluorine

    Each fluorine atom has six electrons, or three pairs of electrons, that are not participating in the covalent bond. Rather than being shared, they are considered to belong to a single atom. These are called nonbonding pairs (or lone pairs) of electrons.

    ADAPT \(\PageIndex{1}\)

     

    Covalent Bonds between Different Atoms

    Now that we have looked at electron sharing between atoms of the same element, let us look at covalent bond formation between atoms of different elements. Consider a molecule composed of one hydrogen atom and one fluorine atom:

    Lewis dot structures of hydrogen (1 dot) and fluorine (7 dots)

    Each atom needs one additional electron to complete its valence shell. By each contributing one electron, they make the following molecule:

    Two representations of a covalent bond in hydrogen fluoride. On the left, a Lewis dot structure shows hydrogen and fluorine with overlapping dashed circles, indicating that each atom contributes one electron to form a shared pair. On the right, the same bond is shown using a line between H and F to represent the shared electron pair, with additional dots around fluorine showing its remaining lone pairs.

    In this molecule, the hydrogen atom does not have nonbonding electrons, while the fluorine atom has six nonbonding electrons (three lone electron pairs). The circles show how the valence electron shells are filled for both atoms.

    Example \(\PageIndex{1}\)

    Draw the Lewis structure for each compound.

    1. a molecule composed of two chlorine atoms
    2. a molecule composed of a hydrogen atom and a bromine atom
    Solution
    1. Chlorine has the same valence shell electron configuration as fluorine, so the Lewis structure for a molecule composed of two chlorine atoms is similar to the one for fluorine:
      Two representations of a chlorine molecule (Cl₂). On the left, a Lewis dot structure shows two chlorine atoms sharing one pair of electrons, with three lone pairs on each atom. On the right, a line-bond structure shows a single bond between the two chlorine atoms, with three lone pairs on each.
    • Bromine has the same valence shell electron configuration as fluorine, so the Lewis structure for a molecule composed of a hydrogen atom and a bromine atom is similar to that for hydrogen and fluorine:
      Two representations of a hydrogen bromide molecule (HBr). On the left, a Lewis dot structure shows hydrogen sharing one pair of electrons with bromine, which has three lone pairs. On the right, a line-bond structure shows a single bond between hydrogen and bromine, with three lone pairs on bromine.
    Exercise \(\PageIndex{1}\)

    Draw the Lewis structure for each compound.

    1. a molecule composed of one chlorine atom and one fluorine atom
    2. a molecule composed of one hydrogen atom and one iodine atom
    Answer a

    Two representations of a chlorine monofluoride molecule (ClF). On the left, a Lewis dot structure shows chlorine and fluorine sharing one pair of electrons; chlorine has three lone pairs and fluorine has three lone pairs. On the right, a line-bond structure shows a single bond between chlorine and fluorine, with three lone pairs on each atom.

    Chlorine monofluoride is a volatile interhalogen compound.

    Answer b

    Two representations of a hydrogen iodide molecule (HI). On the left, a Lewis dot structure shows hydrogen sharing one pair of electrons with iodine, which has three lone pairs. On the right, a line-bond structure shows a single bond between hydrogen and iodine, with three lone pairs on iodine.

    \(\ce{HI}\) is used in organic and inorganic synthesis as one of the primary sources of iodine.

    Larger molecules are constructed in a similar fashion, with some atoms participating in more than one covalent bond. For example, water, with two hydrogen atoms and one oxygen atom can be represented as follows:

    Two representations of the water molecule. On the left, a Lewis dot structure shows oxygen in the center with two lone pairs and single bonds to two hydrogen atoms. On the right, a line‑bond structure shows oxygen bonded to two hydrogens with two lone pairs indicated using dots.

    and methane (CH4), with one carbon atom and four hydrogen atoms, can also be represented as follows:

    Two representations of the methane molecule. On the left, a Lewis dot structure shows carbon in the center bonded to four hydrogen atoms using shared electron pairs. On the right, a line‑bond structure shows carbon bonded to four hydrogens arranged symmetrically around the central atom.
    Figure \(\PageIndex{1}\) shows the number of covalent bonds various atoms typically form.
    Rules for drawing Covalent Lewis Structures

    These apply to either nonmetal/nonmetal or metalloid/nonmetal combinations.

    1. Tally up all valence electrons that are to be used. Remember valence electrons are the Roman numerals above the column the element is located in.
    2. Determine which atom is to be central. Carbon is always central and hydrogen is a terminal atom. If these atoms are not present, then go with the atom you have the least of in the formula (typically this atom is listed first in the formula).
    3. Connect each atom to the central atom using single bonds first.
    4. For simple molecules (molecules with only two atoms), try single bonds, then double, and finally triple to achieve octets around each atom (except for B, Be, and H)
    5. For more complex molecules (3 or more atoms), try one multiple bond at a time if single bonds don't achieve octets on every atom.
    6. My series for molecules/ions that need more than single bonds can be seen below (keeping in mind H, B, and Be only have single bonds)
    • Single/single (\(\ce{-}\), \(\ce{-}\)) ,
    • then single/double (\(\ce{-}\), \(\ce{=}\)),
    • then double/double (\(\ce{=}\), \(\ce{=}\)),
    • and if that does not work try triple/single (\(\ce{#}\), \(\ce{-}\))
    1. In our class, we do not use multiple bonds for halogens.

    Double and Triple Bonds

    In covalent bonding, using double (four total electrons) or triple (six total electrons) is an option to achieve a stable octet. If a single bond does not work, then you may incorporate a multiple bond. Please note the rules above on which atoms will never achieve octets (hydrogen, beryllium and boron). Although it is mathematically feasible, halogens will not use multiple bonds to become stable either.

    Let's look at a few molecules that utilize multiple bonds:

    Three Lewis structures of different molecules. From left to right: formaldehyde, showing carbon double‑bonded to oxygen and single‑bonded to two hydrogens; carbon monoxide, showing a triple bond between carbon and oxygen with lone pairs; and carbon dioxide, showing carbon double‑bonded to two oxygen atoms in a linear arrangement.

    Atoms capable of employing multiple bonds would be oxygen, nitrogen, sulfur, phosphorus, and carbon. If an octet can be achieved with a single bond, do not incorporate multiple bonds into the structure.

    Two Lewis structures of oxygen difluoride are compared. On the left, an incorrect structure shows oxygen double‑bonded to two fluorine atoms. On the right, the correct structure shows oxygen single‑bonded to two fluorine atoms, with lone pairs distributed to satisfy octet rules and minimize formal charge.

    Multiple bonds involve more than one type of connection. For this reason, it is more difficult to break or cleave a multiple bond than it would be a single bond or a bond of a lower order (when comparing the same connected atoms). For example, the triple bond found in carbon monoxide is harder to break than one of the double bonds found in carbon dioxide. When reading about smog production or ozone depletion, consider the bond strengths of the chemicals involved in these environmental problems.

    ADAPT \(\PageIndex{2}\)

    Example \(\PageIndex{1}\)

    Draw the Lewis structure for each molecule: 

    1. O3 (ozone)
    2. N2 (nitrogen)
    3. SO3 (sulfur trioxide)
    4. CCl4 (carbon tetrachloride)

    Solutions

    Four Lewis structures of different molecules. From left to right: ozone, showing three oxygen atoms connected by alternating single and double bonds; nitrogen, showing a triple bond between two nitrogen atoms; sulfur trioxide, showing sulfur bonded to three oxygen atoms with expanded octet representation; and carbon tetrachloride, showing carbon single‑bonded to four chlorine atoms arranged symmetrically.

    ADAPT \(\PageIndex{3}\)

     

    Formula Writing for Covalent Compounds

    Covalent compounds use prefixes to indicate the number of atoms in their formulas. In order to write correct formulas, you will need to memorize Table \(\PageIndex{1}\) below.

    Table \(\PageIndex{1}\): Prefix to occurrence correlations.
    Prefix name Number of Atoms
    Mono 1
    Di (not bi) 2
    Tri 3
    Tetra (not quad) 4
    Penta 5
    Hexa 6
    Hepta (not septa) 7
    Octa 8
    Nona 9
    Deca 10
    Rules for Writing Covalent formulas
    1. There are no charges involved with covalent compounds.
    2. Interpret the prefixes to represent the number of atoms or the subscript.
    3. Do not cross or reduce subscripts (unlike ionic compounds).
    4. The formula should reflect the name of the compound.
    Example \(\PageIndex{1}\)

    Write formulas for the following covalent compounds:

    1. dinitrogen pentoxide
    2. boron trihydride
    3. sulfur hexafluoride
    4. carbon tetrachloride
    5. silicon dioxide
    6. dihydrogen dioxide
    Answer a

    N2O5

    Answer b

    BH3

    Answer c

    SF6

    Answer d

    CCl4

    Answer e

    SiO2

    Answer f

    H2O2, don't reduce subscripts in covalent compounds

     

    ADAPT \(\PageIndex{4}\)

    ADAPT \(\PageIndex{5}\)

    ADAPT \(\PageIndex{6}\)

    Contributors and Attributions


    2.7: Covalent Bonding and Formula Writing is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.

    • Was this article helpful?