Skip to main content
Chemistry LibreTexts

5.8: Polyatomic Molecules- Water, Ammonia, and Methane

  • Page ID
    360450
  • \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

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

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

    ( \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
    • Determine the number of bonds formed by common nonmetal elements.
    • Illustrate covalent bond formation with Lewis electron dot diagrams.

    More than two atoms can participate in covalent bonding, although any given covalent bond will be between two atoms only. Water, ammonia, and methane are common examples that will be discussed in detail below. 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 \(\PageIndex{1}\)).

    Table \(\PageIndex{1}\) The Number of Bonds That Selected Atoms Commonly Form to Other Atoms
    Atom Number of Bonds
    H (group 1) 1
    O (group 16) 2
    N (group 15) 3
    C (group 14) 4

    Water

    Consider H and O atoms:

    8c40de664c623a9a5a5c858f57ea873c.jpg

    The H and O atoms can share an electron to form a covalent bond:

    12e4addcd387cc43e23d0852a8a49c2f.jpg

    The H atom has a complete valence shell. However, the O atom has only seven electrons around it, which is not a complete octet. We fix this by including a second H atom, whose single electron will make a second covalent bond with the O atom:

    f257a538a96ffe13ba6f2f0aa4c12032.jpg

    (It does not matter on what side the second H atom is positioned.) Now the O atom has a complete octet around it, and each H atom has two electrons, filling its valence shell. This is how a water molecule, H2O, is made.

    Ammonia

    The N atom has the following Lewis electron dot diagram:

    It has three unpaired electrons, each of which can make a covalent bond by sharing electrons with an H atom. The electron dot diagram of NH3 is as follows:

    Methane

    The C atom has the following Lewis electron dot diagram:

    :C:

    It has four unpaired electrons, each of which can make a covalent bond by sharing electrons with an H atom. The electron dot diagram of CH4 is as follows:

    clipboard_ee9bd5f574529f3ff037fb445900dcb6b.png

     

     Writing Lewis Structures with the Octet Rule

    For polyatomic molecules, it is helpful to follow the step-by-step procedure outlined here:

     

    1. Determine the total number of valence (outer shell) electrons among all the atoms.
    2. Draw a skeleton structure of the molecule, arranging the atoms around a central atom. (Generally, the element closest to the metals should be placed in the center. There are some exceptions) Connect each atom to the central atom with a single bond (one electron pair).
    3. Distribute the remaining electrons as lone pairs on the terminal atoms (except hydrogen), completing an octet around each atom.
    4. Place all remaining electrons on the central atom.
    5. Rearrange the electrons of the outer atoms to make multiple bonds with the central atom in order to obtain octets wherever possible.

     

    1- Determine the total number of valence (outer shell) electrons in the molecule.

    Since OF2 is a neutral molecule, we simply add the number of valence electrons:

    OF2

       O: 6 valence electrons/atom × 1 atom=6

    + F: 7 valence electrons/atom × 2 atoms=14

    ⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯⎯

                                                               = 20 valence electrons

    2- Draw a skeleton structure of the molecule, arranging the atoms around a central atom and connecting each atom to the central atom with a single (one electron pair) bond.

    As the closest element to the metals, oxygen will be the central atom. After placing 2 single bonds (20 electrons - 4 electrons), we had 16 electrons remaining.

    Fluorine atom attached with a single bond to oxygen, oxygen has another single bond connecting to another fluorine atom

    3- Distribute the remaining electrons as lone pairs on the terminal atoms (except hydrogen) to complete their valence shells with an octet of electrons.

    Each fluorine atom has 6 nonbonding electrons

    4- For OF2, we placed 12 electrons between both Fluorine atoms, leaving 4 to be placed on the central atom:

    4 nonbonding electrons are place on oxygen

    5- Rearrange the electrons of the outer atoms to make multiple bonds with the central atom in order to obtain octets wherever possible.

    In OF2, each atom has an octet as drawn, so nothing changes.

    ParseError: invalid Primary (click for details)
    Callstack:
        at (Courses/De_Anza_College/CHEM_10:_Introduction_to_Chemistry_(Parajon_Puenzo)/05:_Chemical_Bonds/5.08:_Polyatomic_Molecules-_Water_Ammonia_and_Methane), /content/body/div[5]/div[1]/pre, line 2, column 162
    
    ParseError: invalid Primary (click for details)
    Callstack:
        at (Courses/De_Anza_College/CHEM_10:_Introduction_to_Chemistry_(Parajon_Puenzo)/05:_Chemical_Bonds/5.08:_Polyatomic_Molecules-_Water_Ammonia_and_Methane), /content/body/div[5]/div[2]/pre, line 2, column 162
    

    Summary

    In polyatomic molecules, there is a pattern of covalent bonds that different atoms can form.

     

    Contributors and Attributions


    5.8: Polyatomic Molecules- Water, Ammonia, and Methane is shared under a not declared license and was authored, remixed, and/or curated by LibreTexts.

    • Was this article helpful?