Lewis Structures

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Steps to writing Lewis structures

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  • 10 February 2013

    Lewis structures

    Lewis structures are representations of molecules

    showing all electrons, bonding and nonbonding.

    Rules for writing Lewis structures

    Find the sum of valence electrons of all

    atoms in the molecule or polyatomic ion.

    Divide that number by two to get the number

    of electron pairs.

    The central atom is the least electronegative

    element that isnt hydrogen. Connect the

    outer atoms to it by single bonds (e pairs).

    Divide the remaining pairs equally over the

    outer atoms.

    PCl3

    5 + 3(7) = 26

    = 13 pairs

  • 10 February 2013

    Lewis structures

    Place the remaining e-pairs on the

    central atom

    Check for the octet rule, and make

    double or triple bonds if necessary.

    More examples :NH4

    +

    SO3

    CO32-

    HCN

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    Learning check

    Draw Lewis structures for the following

    CO2

    NH3

    N2

    O3

    ClO4-

    SO32-

    HClO2

    HNO3

    HClO4

    H2SO3

    HCNO

    H3PO4

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    Formal charges

    For each atom, count the electrons in lone pairs

    and half the electrons it shares with other atoms.

    Subtract that from the number of valence electrons

    for that atom: The difference is its formal charge.

    The best Lewis structure7

    7is the one with the fewest charges.

    7puts a negative charge on the most electronegative atom.

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    Resonance

    What is the Lewis structure of ozone?

    7but this is at odds with the observed structure of ozone, in which7

    7both bonds are of the same length.

    7both outer oxygens

    have a charge of -1/2.

    The single bond should be longer

    than the double bond7

    The terminal oxygens should

    have formal charges of -1 and 0

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    One Lewis structure cannot accurately

    depict a molecule such as ozone.

    Resonance

    We use multiple structures, resonance

    structures, to describe the molecule.

    Just as green is a synthesis of blue and yellow7

    7ozone is a synthesis of

    these two resonance structures.

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    In truth, the electrons that form the second CO bond in the

    double bonds below do not always sit between that C and that O,

    but rather can move among the two oxygens and the carbon.

    They are not localized,

    but rather are delocalized.

    The organic compound

    benzene, C6H6, has two

    resonance structures.

    It is commonly depicted

    as a hexagon with a circle

    inside to signify the

    delocalized electrons

    in the ring.

    Resonance

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    Exceptions to the octet rule

    There are three types of ions or molecules

    that do not follow the octet rule:

    Ions or molecules with an odd number of electrons.

    Ions or molecules with less than an octet.

    Though relatively rare and usually quite

    unstable and reactive, there are ions and

    molecules with an odd number of electrons.

    NO

    NO2

    O2-

    ClO2

    Also rare. Hydrogen, Helium, Boron, Beryllium

    Non favorable

    Structures !!

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    Ions or molecules with more than eight

    valence electrons (an expanded octet).

    Exceptions to the octet rule

    The only way PCl5 can exist is if

    phosphorus has 10 electrons around it.

    It is allowed to expand the octet of atoms

    on the 3rd row or below.

    Presumably d orbitals in these

    atoms participate in bonding.

    Another example: PO43-

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    Learning check

    Draw resonance structures where appropriate,

    label any formal charges, and rank the resonance

    structures in order of importance to overall structure.

    SCN -

    CS2

    SNF3 S2CO2-

    IO3-

    HCO3-

    PF3

    SO42-

    ClO4-