10.3: Covalent Lewis Structures- Electrons Shared
- Page ID
- 295769
\( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)
\( \newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\)
( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\)
\( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)
\( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\)
\( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)
\( \newcommand{\Span}{\mathrm{span}}\)
\( \newcommand{\id}{\mathrm{id}}\)
\( \newcommand{\Span}{\mathrm{span}}\)
\( \newcommand{\kernel}{\mathrm{null}\,}\)
\( \newcommand{\range}{\mathrm{range}\,}\)
\( \newcommand{\RealPart}{\mathrm{Re}}\)
\( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)
\( \newcommand{\Argument}{\mathrm{Arg}}\)
\( \newcommand{\norm}[1]{\| #1 \|}\)
\( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)
\( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\AA}{\unicode[.8,0]{x212B}}\)
\( \newcommand{\vectorA}[1]{\vec{#1}} % arrow\)
\( \newcommand{\vectorAt}[1]{\vec{\text{#1}}} % arrow\)
\( \newcommand{\vectorB}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vectorC}[1]{\textbf{#1}} \)
\( \newcommand{\vectorD}[1]{\overrightarrow{#1}} \)
\( \newcommand{\vectorDt}[1]{\overrightarrow{\text{#1}}} \)
\( \newcommand{\vectE}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{\mathbf {#1}}}} \)
\( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)
\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)Learning Objectives
- Define covalent bond.
- Illustrate covalent bond formation with Lewis electron dot diagrams.
Ionic bonding typically occurs when it is easy for one atom to lose one or more electrons and another atom to gain one or more electrons. However, some atoms won’t give up or gain electrons easily. Yet they still participate in compound formation. How? There is another mechanism for obtaining a complete valence shell: sharing electrons. When electrons are shared between two atoms, they make a bond called a covalent bond.
Let us illustrate a covalent bond by using H atoms, with the understanding that H atoms need only two electrons to fill the 1s subshell. Each H atom starts with a single electron in its valence shell:
\[\mathbf{H\, \cdot }\; \; \; \; \; \mathbf{\cdot \: H}\]
The two H atoms can share their electrons:
\[\mathbf{H}\: \mathbf{: H}\]
We can use circles to show that each H atom has two electrons around the nucleus, completely filling each atom’s valence shell:
Because each H atom has a filled valence shell, this bond is stable, and we have made a diatomic hydrogen molecule. (This explains why hydrogen is one of the diatomic elements.) For simplicity’s sake, it is not unusual to represent the covalent bond with a dash, instead of with two dots:
H–H
Because two atoms are sharing one pair of electrons, this covalent bond is called a single bond. As another example, consider fluorine. F atoms have seven electrons in their valence shell:
These two atoms can do the same thing that the H atoms did; they share their unpaired electrons to make a covalent bond.
Note that each F atom has a complete octet around it now:
We can also write this using a dash to represent the shared electron pair:
There are two different types of electrons in the fluorine diatomic molecule. The bonding electron pair makes the covalent bond. Each F atom has three other pairs of electrons that do not participate in the bonding; they are called lone pair electrons. Each F atom has one bonding pair and three lone pairs of electrons.
Covalent bonds can be made between different elements as well. One example is HF. Each atom starts out with an odd number of electrons in its valence shell:
The two atoms can share their unpaired electrons to make a covalent bond:
We note that the H atom has a full valence shell with two electrons, while the F atom has a complete octet of electrons.
Example \(\PageIndex{1}\):
Use Lewis electron dot diagrams to illustrate the covalent bond formation in HBr.
Solution
HBr is very similar to HF, except that it has Br instead of F. The atoms are as follows:
![alt](https://chem.libretexts.org/@api/deki/files/355958/10.4.1A.png?revision=1&size=bestfit&width=189&height=74)
The two atoms can share their unpaired electron:
![alt](https://chem.libretexts.org/@api/deki/files/355957/10.4.1B.png?revision=1&size=bestfit&width=324&height=78)
Exercise \(\PageIndex{1}\)
Use Lewis electron dot diagrams to illustrate the covalent bond formation in Cl2.
- Answer
When working with covalent structures, it sometimes looks like you have leftover electrons. You apply the rules you learned so far, and there are still some electrons that remain unattached. You can't just leave them there. So where do you put them?
Multiple Covalent Bonds
Some molecules are not able to satisfy the octet rule by making only single covalent bonds between the atoms. Consider the compound ethene, which has a molecular formula of \(\ce{C_2H_4}\). The carbon atoms are bonded together, with each carbon also being bonded to two hydrogen atoms.
two \(\ce{C}\) atoms \(= 2 \times 4 = 8\) valence electrons
four \(\ce{H}\) atoms \(= 4 \times 1 = 4\) valence electrons
total of 12 valence electrons in the molecule
If the Lewis electron dot structure was drawn with a single bond between the carbon atoms and with the octet rule followed, it would look like this:
![alt](https://chem.libretexts.org/@api/deki/files/78228/CK12_Screenshot_9-4-1.png?revision=1&size=bestfit&width=136&height=108)
This Lewis structure is incorrect because it contains a total of 14 electrons. However, the Lewis structure can be changed by eliminating the lone pairs on the carbon atoms and having to share two pairs instead of only one pair.
![alt](https://chem.libretexts.org/@api/deki/files/78229/CK12_Screenshot_9-4-2.png?revision=1&size=bestfit&width=138&height=71)
A double covalent bond is a covalent bond formed by atoms that share two pairs of electrons. The double covalent bond that occurs between the two carbon atoms in ethane can also be represented by a structural formula and with a molecular model as shown in the figure below.
![alt](https://chem.libretexts.org/@api/deki/files/78230/CK12_Screenshot_9-4-3.png?revision=1&size=bestfit&width=254&height=121)
A triple covalent bond is a covalent bond formed by atoms that share three pairs of electrons. The element nitrogen is a gas that composes the majority of Earth's atmosphere. A nitrogen atom has five valence electrons, which can be shown as one pair and three single electrons. When combining with another nitrogen atom to form a diatomic molecule, the three single electrons on each atom combine to form three shared pairs of electrons.
![alt](https://chem.libretexts.org/@api/deki/files/78231/CK12_Screenshot_9-4-4.png?revision=1&size=bestfit&width=310&height=111)
Each nitrogen atom follows the octet rule with one lone pair of electrons, and six electrons that are shared between the atoms.
Summary
- Covalent bonds are formed when atoms share electrons.
- Lewis electron dot diagrams can be drawn to illustrate covalent bond formation.
- Double bonds or triple bonds between atoms may be necessary to properly illustrate the bonding in some molecules.
Contributions & Attributions
This page was constructed from content via the following contributor(s) and edited (topically or extensively) by the LibreTexts development team to meet platform style, presentation, and quality:
Anonymous by request
Henry Agnew (UC Davis)