LEWIS STRUCTURES
OBJECTIVE
To learn how to draw Lewis structures and
build 3-D molecular (ball-and-stick) models of various compounds.
Determine the shape of each molecule based on the Lewis structure
and 3-D molecular model .
INTRODUCTION
Different types of chemical formulas
One way of representing chemical compounds
is to use their molecular formulas. The only information provided by molecular
formulas is the types of atoms involved in a molecule of a compound and
their relative numbers.
Structural formulas provide additional information
concerning the relative position of atoms in a molecule of a given compound,
or the spacial arrangement of atoms.
In addition to this, Lewis structures indicate
the number and placement of unshared valence electrons. The actual
3-D shapes of molecules may be represented by the ball-and-stick
models in which the balls of various colors represent atoms and the sticks
represent the bonds.
Drawing Lewis structures
Remember that the number of valence electrons
in a main group atom is equal to the number of periodic table group
in which this atom is located. When drawing Lewis structures, keep in mind
that the duet rule applies for hydrogen atoms and the octet is valid
for the majority of other atoms. However, there are exceptions to the octet
rule, particularly when third and lower row elements are considered. Also
remember that some atoms may form multiple bonds ( double or tripple)
The procedure for drawing Lewis structures
is outlined in Chapter 5, page 108, of Fundamentals of General,
Organic, and Biological Chemistry (McMurry and Castellion).
You may also visit this site
for more information.
Ball-and-stick Models.
To build a ball-and-stick model based on
the Lewis structure drawn, use the information organized in Table1.
Molecular shapes.
Molecular shapes may be predicted based on
the number of covalent bonds and the number of lone electron pairs
involving the molecule’s central atom. Please refer to Table 2 to
find the relationship between the number of electron pairs and the molecular
shape. Refer to the lecture text for more information.
Example:
Write a Lewis structure and determine molecular
shape of phosgene (COCl2).
1. Calculate the total number of valence
electrons in COCl2 :
1x 4 (C) + 1 x 6 (O) + 2 x 7 (Cl) = 24
Click
here to see the pictorial representation of step
2, 3 and 8 (to leave this picture, click Back)
2. Carbon is the central
atom in this molecule, therefore other atomic cores are placed as
symetrically as possible around it.
Draw the lines connecting
the central carbon atom with the two chlorine atoms and one
oxygen atom (lines represent
bonding pairs of electrons, single bonds)
3. Add lone pairs of electrons ( two dots
each) to each peripheral atom until the octet is satisfied
for each Cl and O atom.
4. Count electrons surrounding each peripheral
atoms: O 3x2+2= 8, Cl 2 (6 +2)= 16
5. Determine the number of remaining electrons:
24-24= 0. There are no more electrons to be added to atomic cores.
6. Check if all atoms have octet: Cl - does,
O - does , C- has only 6 electrons.
7. Need one more pair of electrons
between C and O to satisfy octet rule for both; use the lone pair
on O to create another bond ( line) between C and O
8. To determine the molecule shape,
count the electron pairs surrounding the central atom ,carbon (C). It is
3, beacuse double bond C=O counts as one bonding electron pair for
the purpose of molecular shape determination.
9. There are no lone pairs present
on the C atom, therefore, based on the info in Table 2, the phosgene
molecule will have the trigonal planar molecular shape ( 3 total electron
pairs with 3 bonding electron pairs), and the bond angle of 120o
Table 1 Table 2
| Atom or bond | Ball color or stick color/hape | Total number of electron pairs | Number of bonds ( or bonding pairs) | Number of lone electron pairs | Bond angle | Molecular shape | Example |
| carbon , C | black |
|
2 | 0 | 180o | linear | BF2 |
| chlorine, Cl | green | 3 | 3 | 0 | 120o | trigonal planar | BF3 |
| hydrogen, | white | 3 | 2 | 1 | <120o | bent or V-shaped | SO2 |
| nitrogen, N | blue | 4 | 4 | 0 | 109.5o | tetrahedral | CH4 |
| oxygen, O | red | 4 | 3 | 1 | <109.5o | trigonal pyramidal | PH3 |
| single bond C-H | short white sticks | 4 | 2 | 2 | 105o | bent | H2O |
| single bond other than C-H | medium-length grey sticks | ||||||
| double or tripple bond | long, flexible grey sticks |
PROCEDURE
1. Obtain a jar with balls and sticks.
Transfer the jar contents to a large beaker or large evaporating
dish. Take care not to spill and loose any balls or sticks!
2. Have your data sheet (see next page)
ready.
3. For each compound, calculate the
total number of valence electrons (record in data table), draw
Lewis structure (in table), build a ball-and-stick model and draw it in
the data table. Then determine the molecular shape and record it
in the data table.
PRELAB QUIZ
Quiz must be taken before the lab.
Late quizzes will not be accepted. You can only take this quiz once.
Instructions:
In the Quiz window, type your instructor's
name in the "Name" box your name and
e-mail address in the "e-mail "box.
For the first four questions click
on circle by the correct answer.
Question 5 requires a written response.
After answering all questions, click Submit
button.
You will see "Thank you" in the screen. You
quiz has been sent to the lab coordinator's e-mail address and will be
forwarded to your instructor.
Click here to
take the quiz
DATA TABLE
| Chemical Formula | Total Number of Valence Electrons | Lewis Structure | Drawing of a ball-and-stick model | Molecular Shape |
|
HCl |
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C2H2
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NH3 |
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H2O
|
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CH2O
|
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| NH4+
|
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CO
|
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| CO2 |
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