4.8: Writing Lewis Structures for Covalent Compounds (2024)

  1. Last updated
  2. Save as PDF
  • Page ID
    492182
  • \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}}}\)

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

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

    ( \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
    • Draw Lewis structures for covalent compounds.

    The following procedure can be used to construct Lewis electron structures for more complex molecules and ions.

    How-to: Constructing Lewis electron structures
    1. Determine the total number of valence electrons in the molecule or ion.
    • Add together the valence electrons from each atom. (Recall that the number of valence electrons is indicated by the position of the element in the periodic table.)
    • If the species is a polyatomic ion, remember to add or subtract the number of electrons necessary to give the total charge on the ion.

    For CO32, for example, we add two electrons to the total because of the −2 charge.

    2. Arrange the atoms to show specific connections.
    • When there is a central atom, it is usually the least electronegative element in the compound. Chemists usually list this central atom first in the chemical formula (as in CCl4 and CO32, which both have C as the central atom), which is another clue to the compound’s structure.
    • Hydrogen and the halogens are almost always connected to only one other atom, so they are usually terminal rather than central.
    3. Place a bonding pair of electrons between each pair of adjacent atoms to give a single bond.
    • In H2O, for example, there is a bonding pair of electrons between oxygen and each hydrogen.

    4. Beginning with the terminal atoms, add enough electrons to each atom to give each atom an octet (two for hydrogen).

    • These electrons will usually be lone pairs.

    5. If any electrons are left over, place them on the central atom.

    • We will explain later that some atoms are able to accommodate more than eight electrons.
    6. If the central atom has fewer electrons than an octet, use lone pairs from terminal atoms to form multiple (double or triple) bonds to the central atom to achieve an octet.
    • This will not change the number of electrons on the terminal atoms.
    7. Final check
    • Always make sure all valence electrons are accounted for and that each atom has an octet of electrons, except for hydrogen (with two electrons).
    • The central atom is usually the least electronegative element in the molecule or ion; hydrogen and the halogens are usually terminal.

    Now let’s apply this procedure to some particular compounds, beginning with one we have already discussed.

    Example \(\PageIndex{1}\): Water

    Write the Lewis Structure for H2O.

    Solution
    Solutions to Example 10.4.1
    Steps for Writing Lewis Structures Example \(\PageIndex{1}\)
    1. Determine the total number of valence electrons in the molecule or ion. Each H atom (group 1) has 1 valence electron, and the O atom (group 16) has 6 valence electrons, for a total of 8 valence electrons.
    2. Arrange the atoms to show specific connections.

    H O H

    Because H atoms are almost always terminal, the arrangement within the molecule must be HOH.

    3. Place a bonding pair of electrons between each pair of adjacent atoms to give a single bond.

    4. Beginning with the terminal atoms, add enough electrons to each atom to give each atom an octet (two for hydrogen).

    Placing one bonding pair of electrons between the O atom and each H atom gives

    H -O- H

    with 4 electrons left over.

    Each H atom has a full valence shell of 2 electrons.

    5. If any electrons are left over, place them on the central atom.

    Adding the remaining 4 electrons to the oxygen (as two lone pairs) gives the following structure:

    4.8: Writing Lewis Structures for Covalent Compounds (1)

    6. If the central atom has fewer electrons than an octet, use lone pairs from terminal atoms to form multiple (double or triple) bonds to the central atom to achieve an octet. Not necessary.
    7. Final check. The Lewis structure gives oxygen an octet and each hydrogen 2 electrons.
    Example \(\PageIndex{2}\)

    Write the Lewis structure for the \(CH_2O\) molecule

    Solution
    Solutions to Example 10.4.2
    Steps for Writing Lewis Structures Example \(\PageIndex{2}\)
    1. Determine the total number of valence electrons in the molecule or ion. Each hydrogen atom (group 1) has 1 valence electron, carbon (group 14) has 4 valence electrons, and oxygen (group 16) has 6 valence electrons, for a total of [(2)(1) + 4 + 6] = 12 valence electrons.
    2. Arrange the atoms to show specific connections.

    4.8: Writing Lewis Structures for Covalent Compounds (2)

    Because carbon is less electronegative than oxygen and hydrogen is normally terminal, C must be the central atom.

    3. Place a bonding pair of electrons between each pair of adjacent atoms to give a single bond.

    Placing a bonding pair of electrons between each pair of bonded atoms gives the following:

    4.8: Writing Lewis Structures for Covalent Compounds (3)

    6 electrons are used, and 6 are left over.

    4. Beginning with the terminal atoms, add enough electrons to each atom to give each atom an octet (two for hydrogen).

    Adding all 6 remaining electrons to oxygen (as three lone pairs) gives the following:

    4.8: Writing Lewis Structures for Covalent Compounds (4)

    Although oxygen now has an octet and each hydrogen has 2 electrons, carbon has only 6 electrons.

    5. If any electrons are left over, place them on the central atom.

    Not necessary.

    There are no electrons left to place on the central atom.

    6. If the central atom has fewer electrons than an octet, use lone pairs from terminal atoms to form multiple (double or triple) bonds to the central atom to achieve an octet.

    To give carbon an octet of electrons, we use one of the lone pairs of electrons on oxygen to form a carbon–oxygen double bond:

    4.8: Writing Lewis Structures for Covalent Compounds (5)

    7. Final check Both the oxygen and the carbon now have an octet of electrons, so this is an acceptable Lewis electron structure. The O has two bonding pairs and two lone pairs, and C has four bonding pairs. This is the structure of formaldehyde, which is used in embalming fluid.
    Exercise \(\PageIndex{1}\)

    Write Lewis electron structures for CO2 and SCl2, a vile-smelling, unstable red liquid that is used in the manufacture of rubber.

    Answer CO2

    .4.8: Writing Lewis Structures for Covalent Compounds (6)

    4.8: Writing Lewis Structures for Covalent Compounds (7)

    Answer SCl2

    .4.8: Writing Lewis Structures for Covalent Compounds (8)

    4.8: Writing Lewis Structures for Covalent Compounds (9)

    The United States Supreme Court has the unenviable task of deciding what the law is. This responsibility can be a major challenge when there is no clear principle involved or where there is a new situation not encountered before. Chemistry faces the same challenge in extending basic concepts to fit a new situation. Drawing of Lewis structures for polyatomic ions uses the same approach, but tweaks the process a little to fit a somewhat different set of circ*mstances.

    Writing Lewis Structures for Polyatomic Ions(CK-12)

    Recall that a polyatomic ion is a group of atoms that are covalently bonded together and which carry an overall electrical charge. The ammonium ion, \(\ce{NH_4^+}\), is formed when a hydrogen ion \(\left( \ce{H^+} \right)\) attaches to the lone pair of an ammonia \(\left( \ce{NH_3} \right)\) molecule in a coordinate covalent bond.

    4.8: Writing Lewis Structures for Covalent Compounds (10)

    When drawing the Lewis structure of a polyatomic ion, the charge of the ion is reflected in the number of total valence electrons in the structure. In the case of the ammonium ion:

    \(1 \: \ce{N}\) atom \(= 5\) valence electrons

    \(4 \: \ce{H}\) atoms \(= 4 \times 1 = 4\) valence electrons

    subtract 1 electron for the \(1+\) charge of the ion

    total of 8 valence electrons in the ion

    It is customary to put the Lewis structure of a polyatomic ion into a large set of brackets, with the charge of the ion as a superscript outside of the brackets.

    Exercise \(\PageIndex{2}\)

    Draw the Lewis electron dot structure for the sulfate ion.

    Answer(CK12 License)
    4.8: Writing Lewis Structures for Covalent Compounds (11)

    Exceptions to the Octet Rule(BC Campus)

    As important and useful as the octet rule is in chemical bonding, there are some well-known violations. This does not mean that the octet rule is useless—quite the contrary. As with many rules, there are exceptions, or violations.

    There are three violations to the octet rule. Odd-electron molecules represent the first violation to the octet rule. Although they are few, some stable compounds have an odd number of electrons in their valence shells. With an odd number of electrons, at least one atom in the molecule will have to violate the octet rule. Examples of stable odd-electron molecules are NO, NO2, and ClO2. The Lewis electron dot diagram for NO is as follows:

    4.8: Writing Lewis Structures for Covalent Compounds (12)

    Although the O atom has an octet of electrons, the N atom has only seven electrons in its valence shell. Although NO is a stable compound, it is very chemically reactive, as are most other odd-electron compounds.

    Electron-deficient molecules represent the second violation to the octet rule. These stable compounds have less than eight electrons around an atom in the molecule. The most common examples are the covalent compounds of beryllium and boron. For example, beryllium can form two covalent bonds, resulting in only four electrons in its valence shell:

    4.8: Writing Lewis Structures for Covalent Compounds (13)

    Boron commonly makes only three covalent bonds, resulting in only six valence electrons around the B atom. A well-known example is BF3:

    4.8: Writing Lewis Structures for Covalent Compounds (14)

    The third violation to the octet rule is found in those compounds with more than eight electrons assigned to their valence shell. These are called expanded valence shell molecules. Such compounds are formed only by central atoms in the third row of the periodic table or beyond that have empty d orbitals in their valence shells that can participate in covalent bonding. One such compound is PF5. The only reasonable Lewis electron dot diagram for this compound has the P atom making five covalent bonds:

    4.8: Writing Lewis Structures for Covalent Compounds (15)

    Formally, the P atom has 10 electrons in its valence shell.

    Example \(\PageIndex{3}\): Octet Violations

    Identify each violation to the octet rule by drawing a Lewis electron dot diagram.

    1. ClO
    2. SF6
    Solution

    a. With one Cl atom and one O atom, this molecule has 6 + 7 = 13 valence electrons, so it is an odd-electron molecule. A Lewis electron dot diagram for this molecule is as follows:

    4.8: Writing Lewis Structures for Covalent Compounds (16)

    b. In SF6, the central S atom makes six covalent bonds to the six surrounding F atoms, so it is an expanded valence shell molecule. Its Lewis electron dot diagram is as follows:

    4.8: Writing Lewis Structures for Covalent Compounds (17)

    Exercise \(\PageIndex{3}\): Xenon Difluoride

    Identify the violation to the octet rule in XeF2 by drawing a Lewis electron dot diagram.

    Answer

    4.8: Writing Lewis Structures for Covalent Compounds (18)

    The Xe atom has an expanded valence shell with more than eight electrons around it.

    Summary

    Lewis dot symbols provide a simple rationalization of why elements form compounds with the observed stoichiometries. A plot of the overall energy of a covalent bond as a function of internuclear distance is identical to a plot of an ionic pair because both result from attractive and repulsive forces between charged entities. In Lewis electron structures, we encounter bonding pairs, which are shared by two atoms, and lone pairs, which are not shared between atoms. Lewis structures for polyatomic ions follow the same rules as those for other covalent compounds. There are three violations to the octet rule: odd-electron molecules, electron-deficient molecules, and expanded valence shell molecules.

    4.8: Writing Lewis Structures for Covalent Compounds (2024)
    Top Articles
    Speech of Ambassador Cavendish at the Commissioning Ceremony for the Piarco Solar Park
    How to Start Investing in Stocks in 2024
    Swissport Timecard
    Yale College Confidential 2027
    Is Whitney Williams Wgem Married
    Royal Bazaar Farmers Market Tuckernuck Drive Richmond Va
    Best Taq 56 Loadout Mw2 Ranked
    Mileage To Walmart
    Craigslist/Phx
    Poochies Liquor Store
    Cratebrowser
    Top Scorers Transfermarkt
    Lesson 10 Homework 5.3
    Apple Store Location
    Bailu Game8
    2023 GMC Yukon Price, Cost-to-Own, Reviews & More | Kelley Blue Book
    Mobile Maher Terminal
    Violent Night Showtimes Near The Riviera Cinema
    North Colonie Continuing Education
    Cloud Cannabis Utica Promo Code
    Ghostbusters Afterlife 123Movies
    Winnie The Pooh Sewing Meme
    Frostbite Blaster
    New Orleans Magazine | Dining, Entertainment, Homes, Lifestyle and all things NOLA
    We Take a Look at Dating Site ThaiFlirting.com in Our Review
    SuperLotto Plus | California State Lottery
    Ck3 Culture Map
    Sona Twu
    Community Q&A with Red Flight and the Combat Box server
    Toonily.cim
    Quattrocento, Italienische Kunst des 15. Jahrhunderts
    Ketchum Who's Gotta Catch Em All Crossword Clue
    Kathy Carrack
    Directions To 401 East Chestnut Street Louisville Kentucky
    Craigslist Labor Gigs Albuquerque
    Stellaris Resolution
    Black Adam Showtimes Near Cinergy Amarillo
    Snowy Hydro Truck Jobs in All Sydney NSW - Sep 2024 | SEEK
    Horseheads Schooltool
    Gargoyle Name Generator
    Edenmodelsva
    Mudae Disable Tags
    Colonial Interceptor
    Sayuri Pilkey
    Jcp Meevo Com
    Alger Grade Ohm
    Download Diablo 2 From Blizzard
    Souvenir Shopping and Local Markets in Belgium
    8 Internet Celebrities who fell prey to Leaked Video Scandals
    Cargurus Button Girl
    Latest Posts
    Article information

    Author: Edwin Metz

    Last Updated:

    Views: 5697

    Rating: 4.8 / 5 (58 voted)

    Reviews: 89% of readers found this page helpful

    Author information

    Name: Edwin Metz

    Birthday: 1997-04-16

    Address: 51593 Leanne Light, Kuphalmouth, DE 50012-5183

    Phone: +639107620957

    Job: Corporate Banking Technician

    Hobby: Reading, scrapbook, role-playing games, Fishing, Fishing, Scuba diving, Beekeeping

    Introduction: My name is Edwin Metz, I am a fair, energetic, helpful, brave, outstanding, nice, helpful person who loves writing and wants to share my knowledge and understanding with you.