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11/12/22, 11:32 PM
VSEPR and MO Diagrams Workshop Activity - Nov 7th/8th (Workshop 10)
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VSEPR and MO Diagrams Workshop Activity - Nov 7th/8th (Workshop 10)
Due: 12:00am on Monday, December 12, 2022
You will receive no credit for items you complete after the assignment is due. Grading Policy
Exercise 11.32 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.2 (Page) ; Watch KCV 11.2
, IWE 11.1
.
A molecule with the formula has a trigonal planar geometry.
Part A
How many electron groups
are on the central atom?
Express your answer as an integer.
ANSWER:
Exercise 11.34 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.2 (Page) , 11.3 (Page) ; Watch KCV 11.2
, 11.3
, IWE 11.1
, 11.2
.
The following figures show several molecular geometries.
Part A
Give the number of total electron groups, the number of bonding groups, and the number of lone pairs for the geometry depicted in (a).
Express your answers as integers separated by commas.
ANSWER:
Part B
Give the number of total electron groups, the number of bonding groups, and the number of lone pairs for the geometry depicted in (b).
Express your answers as integers separated by commas.
ANSWER:
Part C
Give the number of total electron groups, the number of bonding groups, and the number of lone pairs for the geometry depicted in (c).
Express your answers as integers separated by commas.
ANSWER:
electron groups
, , =
, , =
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Exercise 11.36 - Enhanced - with Feedback
MISSED THIS?
Read section 11.3 (Page) , 11.4 (Page) ; Watch KCV 11.3
, IWE 11.2
.
Determine the electron geometry, molecular geometry, and idealized bond angles for each of the following molecules.
a. b. c. d. In which cases do you expect deviations from the idealized bond angle?
Part A
Determine the electron geometry for each molecule.
Drag the appropriate items to their respective bins.
ANSWER:
Part B
Determine the molecular geometry for each molecule.
Drag the appropriate items to their respective bins.
ANSWER:
, , =
Reset
Help
Linear
Tetrahedral
Trigonal planar
Trigonal bipyramidal
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Part C
Determine the idealized bond angle for each molecule.
Drag the appropriate items to their respective bins.
ANSWER:
Part D
In which cases do you expect deviations from the idealized bond angle?
Check all that apply.
ANSWER:
Reset
Help
Reset
Help
Tetrahedral
Trigonal pyramidal
Bent
Linear
90
180
109.5
120
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Exercise 11.39 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.3 (Page) , 11.4 (Page) ; Watch KCV 11.3
, IWE 11.2
.
Part A
Determine the molecular geometry for .
ANSWER:
Correct
has 34 valence electrons (6 on sulfur + (4
7) on the fluorine). There are five electron groups around the sulfur atom: four bonding groups and one
lone pair. This means that the
atoms has a seesaw molecular geometry.
Part B
Determine the molecular geometry for .
ANSWER:
Correct
The Lewis structure for
has 28 valence electrons. There are five electrons groups around the
atom: three bonding groups and two lone pairs.
The molecular geometry for
is T-shaped.
Part C
Determine the molecular geometry .
ANSWER:
trigonal bipyramidal
square planar
T-shape
seesaw
square pyramidal
seesaw
square planar
T-shape
square pyramidal
trigonal bipyramidal
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VSEPR and MO Diagrams Workshop Activity - Nov 7th/8th (Workshop 10)
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Correct
The Lewis structure for
has 22 valence electrons. There are five electrons groups around the central
atom: two bonding groups and three lone
pairs. The molecular geometry for
is linear.
Part D
Determine the molecular geometry .
ANSWER:
Correct
The
ion has 36 valence electrons. There are six electron groups around the central
atom: four bonding groups and two lone pairs. The molecular
geometry for
is square planar.
Part E
For each molecule or ion choose the appropriate sketch.
Drag the appropriate labels to their respective targets.
ANSWER:
bent
seesaw
trigonal bipyramidal
linear
T-shape
square pyramidal
trigonal bipyramidal
seesaw
square planar
octahedral
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Exercise 11.48 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.5 (Page) ; Watch KCV 11.5
, IWE 11.5
.
is a polar molecule, even though the tetrahedral geometry often leads to nonpolar molecules.
Part A
Draw the Lewis structure of .
Draw the molecule by placing atoms on the grid and connecting them with bonds. Include all lone pairs of electrons and all hydrogen atoms.
ANSWER:
Help
Reset
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Part B Complete previous part(s)
Exercise 11.50 - Enhanced - with Feedback and Hints
MISSED THIS?
Read Section 11.5 (Page) ; Watch KCV 11.5
, IWE 11.5
.
Part A
Determine whether each molecule given below is polar or nonpolar.
Drag the appropriate items to their respective bins.
You did not open hints for this part.
ANSWER:
+
-
C
H
O
N
S
P
F
Br
Cl
I
X
More
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VSEPR and MO Diagrams Workshop Activity - Nov 7th/8th (Workshop 10)
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Exercise 11.52 - Enhanced - with Feedback and Hints
MISSED THIS?
Read Section 11.5 (Page) ; Watch KCV 11.5
, IWE 11.5
.
Part A
Determine whether each molecule is polar or nonpolar.
Drag the appropriate items to their respective bins.
You did not open hints for this part.
ANSWER:
Reset
Help
Reset
Help
Polar
Nonpolar
Nonpolar
Polar
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Exercise 11.53 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.6 (Page) ; Watch KCV 11.6
.
The valence electron configurations of several atoms are shown. How many bonds can each atom make without hybridization?
Part A
Express your answer as an integer.
ANSWER:
Part B
Express your answer as an integer.
ANSWER:
Part C
Express your answer as an integer.
ANSWER:
Exercise 11.59 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.7 (Page) ; Watch KCV 11.7
.
Part A
Which of the following hybridization schemes allows the formation of at least one bond?
Check all that apply.
ANSWER:
Exercise 11.60 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.7 (Page) ; Watch KCV 11.7
.
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Part A
Which of the following hybridization schemes allows the central atom to form more than four bonds? ANSWER:
Exercise 11.62 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.7 (Page) ; Watch KCV 11.7
, IWE 11.8 .
Write a hybridization and bonding scheme for each molecule.
Part A
Identify the hybridization of the atom in .
ANSWER:
Correct
To allow bonding with four other atoms, the carbon atom must hybridize its four valence orbitals to equally accommodate each bond.
Part B
In the sketch of the structure of label all bonds.
Drag the appropriate labels to their respective targets. Labels can be used once, more than once, or not at all.
ANSWER:
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Part C
Identify the hybridization of the atom in .
ANSWER:
Correct
The standard atomic orbitals of sulfur has one filled orbital, one filled orbital, and two partially filled orbitals. To accommodate a lone pair and
bonding with two oxygen atoms (i.e., three
electron groups), the valence orbitals of sulfur are hybridized to , which leaves an unhybridized orbital.
Part D
In the sketch of the structure of label all bonds.
Drag the appropriate labels to their respective targets. Labels can be used once, more than once, or not at all.
ANSWER:
Help
Reset
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Part E
Identify the hybridization of the atom in .
ANSWER:
Correct
Part F
In the sketch of the structure of label all bonds.
Drag the appropriate labels to their respective targets. Labels can be used once, more than once, or not at all.
ANSWER:
Help
Reset
Lone pair in orbital
Lone pair in orbital
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Part G
Identify the hybridization of the atom in .
ANSWER:
Correct
For each atom to have a formal charge of 0, the valence shell of boron is only partially filled. The valence orbital and two of the valence orbitals of
boron hybridize to form three equivalent orbitals.
Part H
In the sketch of the structure of label all bonds.
Drag the appropriate labels to their respective targets. Labels can be used once, more than once, or not at all.
ANSWER:
Help
Reset
Lone pair in orbital
Lone pair in orbital
Lone pair in orbital
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Exercise 11.67 - Enhanced - with Feedback and Hints
MISSED THIS?
Read Section 11.7 (Page) ; Watch KCV 11.7
, IWE 11.8 .
Part A
Consider the structure of the amino acid alanine. Indicate the hybridization about each interior atom.
Drag the labels to the appropriate targets.
You did not open hints for this part.
ANSWER:
Help
Reset
Empty orbital
Empty orbital
Lone pair in orbital
Lone pair in orbital
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Exercise 11.68 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.7 (Page) ; Watch KCV 11.7
, IWE 11.8
.
Part A
Consider the structure of the amino acid aspartic acid. Indicate the hybridization about each interior atom.
Drag the appropriate labels to their respective targets.
ANSWER:
Help
Reset
Help
Reset
sp
sp
2
sp
3
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Exercise 11.72 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.8 (Page) ; Watch IWE 11.10
.
Part A
Complete the atomic orbital (AO) and molecular orbital (MO) energy diagram for .
Drag the appropriate labels to their respective targets.
ANSWER:
Part B
Complete the AO and MO energy diagram for . Assume the left AO comes from and the right AO comes from .
Drag the appropriate labels to their respective targets.
ANSWER:
Help
Reset
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Part C Complete previous part(s)
Part D Complete previous part(s)
PhET Simulation - Molecule Shapes
The shapes of molecules depend on the number of electron groups that surround a central atom. For molecules in which all electrons around the central atom are
participating in bonding, the molecular geometry is the same as the electron geometry, and the molecular shapes are linear, trigonal planar, tetrahedral, trigonal
bipyramidal, and octahedral. However, nonbonded electrons, which wouldn't be observed in the molecular geometry, affect the overall distribution of electron groups;
therefore, the molecular and electron geometries will be different when nonbonding electrons are present.
This can be exemplified in the case of ammonia, . Ammonia has three bonding groups, but it will not exhibit trigonal planar
geometry because the lone pair of
electrons exerts a repulsive force. There are four electron groups (three bonding groups and one nonbonding group) in ammonia, which means that the electron
geometry will be tetrahedral
. When only the molecular structure is examined, the lone pair is not seen, and the molecular geometry will adopt a more pyramidal structure
that can be seen in the image below (
trigonal pyramidal
).
Electron geometry of is tetrahedral
Molecular geometry of is trigonal pyramidal
The valence-shell electron-pair repulsion
(VSEPR) model encompasses the geometries that result from the various interactions that occur between electron groups
(also called electron domains
) and the relative repulsive forces exerted by each type of electron group (lone pair, single bond, double bond, and triple bond). VSEPR
models also predict both the electron and molecular geometries, but not all reference charts may indicate bond angles.
Click on the image to explore this simulation
, which allows you to build molecules with lone pairs and various types of bonds while showing the resulting geometries.
When you click the simulation link, you may be asked whether to run, open, or save the file. Choose to run or open it.
Help
Reset
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When the simulation is opened, you will the option for Model
or Real Molecules
modes. In the Model
mode, you can add single, double, and triple bonds as well as
remove them using the Bonding
box. Lone pairs can be added or removed using the Lone Pair
box. If you want to easily reset the molecule, click the Remove All
button to have just the central atom displayed. There are also checkbox options for showing lone pairs and bonding angles (when they exist) and the applicable
Molecule Geometry
and Electron Geometry
. In the Real Molecules
mode, you have the same options that existed in the Model
mode, but the displayed molecule is
selected from a dropdown menu. The radio buttons labeled Real
and Model
that are centered at the top alters the display in the following manner: The color of each
atom is generic in the model view, but colors are specific to each element in the real view; the predicted bond angles based on geometry are shown in the model view,
but the experimentally observed bond angles are shown in the real view.
Part A
The simulation shows the electron and molecular geometries for a variety of compounds. For example, click the Real Molecules
mode and select as the
molecule. Check the boxes marked Show Lone Pairs
(under Options
to the right) as well as Molecule Geometry
and Electron Geometry
(under Name
in the
bottom left), and the respective geometries should display, which are Square Pyramidal
and Octahedral
, respectively. The structure of bromine pentafluoride
consists of one lone pair and five single bonds.
You can recreate this molecule in the Model
mode by adding a single lone pair and five single bonds to the central atom (click the Remove All
button to start over).
You will have successfully recreated the molecule if the displayed molecular and electron geometries are square pyramidal and octahedral, respectively. Use the
Model
mode in the simulation to identify the geometries for ozone, phosphate ion, and argon fluorohydride (for which the Lewis structures are depicted, and the
resonance forms can be ignored).
Drag the labels to the respective targets
You did not open hints for this part.
ANSWER:
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Bond angles
The types of electron groups not only affect the electron and molecular geometries but have differing effects on bond angles. Lone pairs of electrons repulse other
electron groups more strongly than single bonds. For instance, four single bonds in a tetrahedral formation will yield 109.5
bond angles because all bonds equally
repulse each other. In the case of three single bonds and one lone pair (e.g., in , the electron geometry is tetrahedral, and the molecular geometry is trigonal
pyramidal), the bond angle between the three single bonds will actually be more acute than the predicted 109.5
(instead, they are 107.8
) because the repulsion from
the lone pair forces the bonds closer together.
This behavior can also be seen in the simulation. Click the Real Molecules
mode, and select as the molecule. Check the box marked Show Bond Angles
, and
switch between the Real
and Model
radio buttons centered at the top of the simulation. What is being demonstrated is the increased repulsion of lone pairs, and that is
why the model predicts 109.5
, and the actual bond angle is 104.5
. These differences in the bond angles can be seen for the following compounds in the simulation: , , , , , and . There are no changes to predicted bond angles when all the bonds are in the same plane because the lone pairs are
equally repulsing on each side of the plane, which occurs in the case of and .
Part B
Consider the following pairs of molecules that have the same electron geometries. Based on your observations between the Model
and Real
bond angles in the
PhET simulation, complete the sentences to accurately compare the bond angles in each molecule.
Match the words in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting
your answer.
You did not open hints for this part.
ANSWER:
Help
Reset
seesaw
linear
trigonal planar
T-shaped
bent
trigonal bipyramidal
square planar
octahedral
square pyramidal
tetrahedral
trigonal pyramidal
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Effects of electronegativity in molecular bonds
When atoms participate in a covalent bond, the electrons they share are not always evenly distributed within that bond. Electronegativity describes the tendency for an
atom to draw electrons toward its nucleus. When there is a significant enough difference between the electronegativities of two atoms, the bond is considered polar
covalent
since the electrons spend more time near the more electronegative nucleus. In a polar covalent bond, the less electronegative atom will have a partial positive
charge (
), and the more electronegative atom will have a partial negative charge (
). If there is no significant difference between the electronegativities of the
atoms, then the bond is considered nonpolar covalent
(and the nonpolar aspect can be characterized by the symbol). Finally, when the electronegativity difference is
very large, ionic bonds tend to form instead of covalent bonds. The table below summarizes how to classify bonds based on the numeric difference between the Pauling
electronegativity values of atoms.
Pauling
electronegativity
difference
Type of
bond
<0.4
Nonpolar
covalent
0.4 to 1.7
Polar
covalent
>1.7
Ionic
Part C
The structures of , , and are provided below along with the Pauling electronegativity values of , , and . Use the figure and values to complete
the following statements regarding the polarity of bonds in water, carbon dioxide, and methane.
Element
Pauling
electronegativity
2.55
2.20
3.44
Match the words in the left column to the appropriate blanks in the sentences on the right. Make certain each sentence is complete before submitting
your answer.
You did not open hints for this part.
ANSWER:
Reset
Help
less than
equal to
greater than
The bond angle in is the bond angle in .
The bond angle in is the bond angle in .
The T-junction
(one axial and one equatorial T atom) bond angle in is the T-junction
bond angle in .
The bond angle in is the bond angle in .
The bond angle in is the bond angle in .
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Polar molecules and their dependence on geometry
Molecular geometry impacts whether a molecule is polar. Polarity is important because polar molecules interact more strongly with each other (intermolecular
interaction) than nonpolar molecules. This explains why nonpolar molecules tend to be gases at room temperature and why polar molecules tend to be liquids at room
temperature. Stronger intermolecular forces require more energy to separate them from each other.
The molecular geometry and bond polarities both
play critical roles in determining whether or not a molecule is polar. A polar molecule has a net
dipole moment, which
means that there is an uneven distribution of electrons across the entire molecular structure. This dipole moment is sometimes indicated by an arrow, which has a cross
at the end of the lowest electron density (positive end) and points in the direction of the highest electron density (negative end). This dipole moment is achieved when
the molecule's polar covalent bonds have an asymmetric orientation. Examine the structures of carbon dioxide and carbonyl sulfide below. Both molecules contain at
least one polar covalent bond, but only is symmetric. The asymmetry in is due to oxygen being more electronegative than sulfur. As you can see, the
symmetry in effectively cancels out all bond dipole moments, but a net dipole moment can exist in because of its asymmetry.
Part D
Examine the three-dimensional structures of each of the following molecules in the simulation, which can be found in the Real Molecules
mode. Then, identify
which molecules are polar and which are nonpolar. Assume that every bond in each molecule is polar covalent. It may be easier to visualize if you uncheck the box
labeled Show Lone Pairs
.
Drag the appropriate items to their respective bins.
You did not open hints for this part.
ANSWER:
Reset
Help
ionic
more
polar
nonpolar
less
1. For the water molecule, oxygen is electronegative than hydrogen.
2. The difference in electronegativity signifies that the hydrogen-oxygen bond
is .
3. According to the electronegativity difference between the atoms in water, it would be appropriate to label
hydrogen with the symbol and oxygen with the symbol .
4. Based on the electronegativity difference between carbon and oxygen, the bonds
in carbon dioxide are .
5. According to the electronegativity difference between the atoms in carbon dioxide, it would be appropriate
to label oxygen with the symbol and carbon with the symbol .
6. Based on the electronegativity difference between carbon and hydrogen, the bonds
in methane are .
7. According to the electronegativity difference between the atoms in methane, it would be appropriate to
label hydrogen with the symbol and carbon with the symbol .
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PhET Simulation – Molecule Polarity
Electronegativity is a term used to define an atom’s ability to attract electrons to itself when it is bonded to another atom. A larger electronegativity value indicates a
greater ability for an atom to attract electrons to itself. Electronegativity values follow trends (with exceptions) across the periodic table. They increase from left to right
across a period and increase from the bottom of a group to the top. Thus, fluorine is the most electronegative element with a value of 4.0. Notice that since the noble
gases have completely filled electron shells and are inert, they don’t have assigned electronegativity values.
In any given molecule comprised of two or more nonidentical atoms, the electrons contained in the bond are not shared equally. Bond polarity is a measure of how
unevenly the electrons in a bond are shared and is indicated by the difference between the electronegativities of the atoms involved. A large difference in
electronegativities indicates that a bond is polar and contains a dipole (i.e., the bond character is more ionic), which is created when two equal but opposite charges are
separated. A smaller difference in electronegativity makes the bond character more covalent.
Click on the image below to explore this simulation
, which demonstrates the cause and effect of molecular polarity. When you click this simulation link, you may be
asked whether to run, open, or save the file. Choose to run or open it.
When the simulation is opened you should select the option for Two Atoms
. You will then see two atoms (A and B) with a dipole moment drawn directly over the bond.
As the electronegativity for each atom is adjusted using the sliders above, the dipole moment arrow will grow, shrink, or change directions. There are check boxes to the
right of the molecule to control whether bond dipoles, partial charges, or bond character are displayed. There are also switches to control the display of electrostatic
potential, the display of electron density, and the ability to enable an electric field. Clicking the Three Atoms
tab brings up a similar display but with an additional atom.
Clicking the Real Molecules
tab enables you to view the properties of various real compounds.
Part A
In the PhET simulation window, click the Two Atoms
option. Click on the partial charges check box to see the partial charges of the atoms. Vary the
electronegativity of atom A and atom B and observe the effects on the partial charge of each accordingly.
Use the PhET to complete the sentences describing how electronegativity is related to bond dipole experienced by the molecule.
Reset
Help
Polar
Nonpolar
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Match the words to the appropriate blanks in the sentences below. Make certain each sentence is complete before submitting your answer.
You did not open hints for this part.
ANSWER:
Bond polarity
Bond polarity results from two bonded atoms having differing electronegativity values. Covalent
bonds exist when the two atoms involved in the bond share the
electrons. These electrons are shared either evenly or unevenly to a degree depending on the electronegativity differences between the two atoms. Ionic
bonds exist
when the two atoms transfer electrons. These electrons are so strongly attracted to the more electronegative atom that there is virtually no sharing of electrons and the
atoms are simply attracted to another by having opposite charges.
The difference in electronegativity values can be used to predict the type of bond formed between two atoms.
Nonpolar covalent
: Bonds between atoms with electronegativity differences of 0.4 and under are generally considered nonpolar covalent bonds since the
electrons are shared relatively evenly. This is true even if there are two different atoms in the bond, such as a bond.
Polar covalent
: Bonds between atoms with electronegativity differences between 0.4 and 2.0 are generally considered polar covalent since the electrons
are shared unevenly.
Ionic
: Bonds between atoms with electronegativity differences greater than 2.0 are generally considered ionic since the electrons are localized on the
more electronegative atom.
Part B
Using the given table of electronegativity values, determine whether each bond is nonpolar covalent, polar covalent, or ionic.
Element
Electronegativity
Element
Electronegativity
4.0
2.5
3.5
2.5
3.0
2.1
2.9
1.6
2.7
0.9
2.6
0.8
Drag the appropriate items to their respective bins.
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ANSWER:
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more
less
increase
negative
positive
lowest
ionic
highest
decrease
covalent
dipole
1. When two atoms with different electronegativities are bonded together, a bond exists.
These are displayed with an arrow originating at the atom with the electronegativity and
pointing toward the atom with the electronegativity.
2. Partial charges will exist on each atom when a bond exists between two atoms with different
electronegativities. Since the atom with a higher electronegativity will have a stronger ability to attract
electrons, it will have a partial charge. The atom with a lower electronegativity will have
an equal and opposite charge. As the difference in electronegativity increases, the
resulting magnitudes of the partial charges will .
3. Bond character is used to describe the severity of the electronegativity differences between the two
atoms involved in a bond. Bonds that have character correspond to a larger difference
in electronegativities, and bond character corresponds to a smaller difference.
4. For example, if the electronegativity of both atom "A" and "B" in the PhET are set to be equivalent,
then increasing the electronegativity of atom "A" in the PhET simulation and decreasing the
electronegativity of atom "B" will result in a bond that is ionic in character.
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Molecular dipoles and shape
Molecular dipoles are overall dipoles for an entire molecule that result from individual bond dipoles and molecular shape. For molecules where the shape is uncertain,
Lewis structures can be used to predict molecular geometry.
If the only bond dipoles that exist are equal in magnitude and opposite in direction, then there is no molecular dipole and the molecule is considered nonpolar. If bond
dipoles exist and this is not the case, then the molecule has a molecular dipole and it is considered polar. For example, since the molecule below is linear and the
dipoles are equal and opposite, they cancel out, leaving the molecule nonpolar with no net molecule dipole. However, if instead the molecule contained atoms , ,
and , where the bond dipoles for and were not equal, we would expect a molecule dipole and a polar molecule.
Keep in mind there are instances in which a molecule can be made of a single element and still have a molecular dipole. For example, ozone contains a molecular
dipole because the electrons involved in the bonds between the oxygen atoms are unequally shared, and its molecular shape doesn't place the resulting dipoles in
equally opposite directions.
The electrons involved in the bonds of ozone are shared unequally because the central oxygen atom has to share electrons with the two oxygen atoms on the ends,
while the others only have to share electrons with the central atom. This gives the central oxygen a slight positive partial charge.
Part C
NOTE: The simulation required for this part uses Java, and is therefore not screen-reader accessible and may not work on a mobile device. If the browser you’re
using no longer supports Java, try a different browser and download the Java plugin for this content.
In the PhET simulation window, click the Real Molecules
option. Select the corresponding molecule and click on the molecular dipole check box in the View
menu on the right. Use the Molecule
dropdown box to choose a different molecule.
Indicate whether each molecule is polar or nonpolar.
Drag the appropriate items to their appropriate bins.
You did not open hints for this part.
ANSWER:
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Help
bond between and bond between and bond between and bond between and bond between and bond between and bond between and bond between and bond between and bond between and Nonpolar covalent
Polar covalent
Ionic
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Electric field
Electric fields can orient molecules based upon their molecular dipoles and partial charges. Positive partial charges will align toward the negative end of the electric
field, and negative charges will align toward the positive end of the field.
Part D
In the PhET simulation window, click the Three Atoms
option. Drag the switch to "on" under Electric Field
. Vary the shape and electronegativity of each atom to
observe the effect of the electric field. After experimenting with the PhET, draw a molecule of dibromomethane (
). Use this drawing to assign partial charges and determine whether or not the
molecule is polar.
Color
Element
Electronegativity
Dark
gray
(large)
Carbon
2.5
Light
gray
(small
Hydrogen
2.1
Brown
Bromine
2.9
The positive plate is on the right, and the negative plate is on the left. An electric field is set up between the plates. The molecule will orient according to the electric
field to minimize charge distribution. Complete the diagram showing how dibromomethane (
) will orient itself in an electric field according to partial positive
and negative charges.
Drag the appropriate labels to their respective targets.
You did not open hints for this part.
ANSWER:
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Help
Polar molecules
Nonpolar molecules
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Exercise 11.31 - Enhanced - with Feedback
MISSED THIS?
Read Section 11.2 (Page) ; Watch KCV 11.2
, IWE 11.1 .
A molecule with the formula has a trigonal pyramidal geometry.
Part A
How many electron groups are on the central atom (
)?
Express your answer as an integer.
ANSWER:
Chapter 11 Algorithmic Question 9
Part A
Determine the electron geometry (eg) and molecular geometry (mg) of SiF
4
.
ANSWER:
Help
Reset
Group 2
Group 1
Group 1
Group 3
Group 3
Group 3
Group 3
Group 1
Group 1
polar
nonpolar
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Correct
Chapter 11 Algorithmic Question 10
Part A
Determine the electron geometry (eg) and molecular geometry (mg) of PF
5
.
ANSWER:
Correct
Chapter 11 Algorithmic Question 14
Part A
Identify which of the following statements best describes ClBr
2
- ?
ANSWER:
Correct
Chapter 11 Algorithmic Question 19
eg = tetrahedral, mg = tetrahedral
eg = octahedral, mg = trigonal bipyramidal
eg = tetrahedral, mg = bent
eg = trigonal bipyramidal, mg = trigonal bipyramidal
eg = tetrahedral, mg = trigonal pyramidal
eg = trigonal planar, mg = trigonal pyramidal
eg = tetrahedral, mg = trigonal pyramidal
eg = trigonal bipyramidal, mg = trigonal bipyramidal
eg = octahedral, mg = square pyramidal
eg = trigonal bipyramidal, mg = trigonal pyramidal
It has a molecular geometry that is
linear with lone pairs on the Cl atom.
linear with no lone pairs on the Cl atom.
trigonal pyramidal with lone pairs on the Cl atom.
square planar with no lone pairs on the Cl atom.
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Part A
Determine the electron geometry (eg) and molecular geometry (mg) of XeF
2
.
ANSWER:
Correct
Chapter 11 Algorithmic Question 20
Part A
Determine the electron geometry (eg) and molecular geometry (mg) of KrF
4
.
ANSWER:
Correct
Chapter 11 Algorithmic Question 24
Part A
What is the molecular geometry of IF
4
-
?
ANSWER:
eg = tetrahedral, mg = bent
eg = trigonal bipyramidal, mg = tetrahedral
eg = tetrahedral, mg = tetrahedral
eg = trigonal bipyramidal, mg = linear
eg = linear, mg = trigonal pyramidal
eg = trigonal bipyramidal, mg = square planar
eg = tetrahedral, mg = trigonal pyramidal
eg = octahedral, mg = square planar
eg = tetrahedral, mg = square planar
eg = linear, eg = square planar
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Correct
Chapter 11 Algorithmic Question 38
Part A
What is the O-S-O bond angle in SO
3
?
ANSWER:
Correct
Chapter 11 Algorithmic Question 48
Part A
Determine the electron geometry (eg), molecular geometry (mg), and polarity of N
2
O (N central).
ANSWER:
Correct
Chapter 11 Algorithmic Question 45
trigonal bipyramidal
tetrahedral
square pyramidal
square planar
seesaw
109.5°
107°
60°
120°
240°
eg = linear, mg = linear, nonpolar
eg = trigonal planar, mg = linear, nonpolar
eg = tetrahedral, mg = bent, polar
eg = linear, mg = linear, polar
eg = tetrahedral, mg = linear, nonpolar
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Part A
Choose the compound below that contains at least one polar covalent bond, but is nonpolar.
ANSWER:
Correct
Chapter 11 Algorithmic Question 55
Part A
The orbital hybridization on the carbon atoms in SCN
-
is
ANSWER:
Correct
Chapter 11 Algorithmic Question 57
Part A
The hybrid orbital set used by the central atom in BrO
3
-
is ________.
ANSWER:
AsBr
5
GeH
2
Br
2
SCl
2
CH
2
Cl
2
All of the above are nonpolar and contain a polar covalent bond.
sp.
sp
3
d.
sp
2
.
sp
3
.
sp
2
d.
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Correct
Chapter 11 Algorithmic Question 61
Part A
A molecule containing a central atom with sp hybridization has a ________ electron geometry.
ANSWER:
Correct
Chapter 11 Algorithmic Question 76
Part A
Give the electron geometry (eg), molecular geometry (mg), and hybridization for H
2
O.
ANSWER:
Chapter 11 Multiple Choice Question 36
sp
sp
3
d
2
sp
2
sp
3
d
sp
3
T-shaped
linear
square pyramidal
tetrahedral
trigonal bipyramidal
eg = trigonal pyramidal, mg = bent, sp
3
eg = tetrahedral, mg = bent, sp
3
eg = bent, mg = trigonal bipyramidal, sp
2
eg = trigonal planar, mg = tetrahedral, sp
2
eg = tetrahedral, mg = trigonal pyramidal, sp
3
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Part A
Give the hybridization for the Br in BrCl
3
.
ANSWER:
Chapter 11 Multiple Choice Question 38
Part A
Give the hybridization for the C in H
2
CCH
2
.
ANSWER:
Chapter 11 Multiple Choice Question 43
Part A
Use the molecular orbital diagram shown to determine which of the following is most stable.
sp
3
sp
sp
3
d
2
sp
2
sp
3
d
sp
3
sp
3
d
2
sp
sp
3
d
sp
2
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ANSWER:
Chapter 11 Multiple Choice Question 46
Part A
Draw the molecular orbital diagram shown to determine which of the following is paramagnetic.
ANSWER:
Score Summary:
Your score on this assignment is 16.5%.
You received 5.63 out of a possible total of 34 points.
N
2
2
+
C
2
2
-
B
2
2
+
C
2
2
+
B
2
O
2
2+
F
2
2+
Ne
2
2+
O
2
2-
None of the above are paramagnetic.
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Construct the expression for Kc for the following reaction.
4 HCI(aq) + O:(g) = 2 H:O(I) + 2 Cl:(g)
1
Drag the tiles into the numerator or denominator to form the expression. Each reaction
participant must be represented by one tile. Do not combine terms.
Kc
5 RESET
[HCI]
2[HCI]
4[HCI]
[HCIP
[HCIJ*
[0:]
2[0:]
4[O:]
[H:O]
2[HŁO]
4[H.O]
[H:OJ
[CL]
2[CL]
4[CL]
[CL*
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SCH4U-Unit 3 Assignment-2023
1. Calculate AH for the reaction: HCl(g) + NaNO2(s)→ HNO2(1) + NaCl(s)
using the following data:
Reaction
2NaCl(s) + H₂O(1)→ 2HCI(g) + Na₂O(s)
NO(g) + NO₂(g) + Na₂O(s)→ 2NaNO₂(s)
NO(g) + NO₂(g) →N₂O(g) + O2(g)
2HNO2(1)→→ N₂O(g) + O2(g) + H₂O(1)
ΔΗ(kJ)
382.0
-601.0
-40.0
Page 2 of 6
29.0
2. A 5.81g sample of quinone, C6H4O2, was burned in excess oxygen in a
calorimeter. The heat capacity of the calorimeter is calibrated to 4.24 kJ/°C.
Calculate the molar enthalpy of combustion if the temperature of the
calorimeter increased from 17.0 °C to 38.0 °C.
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Read and interpret the following information using the following abstract from a scientific journal article. In 2-3 sentences, summarize what you understand from this research
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A&P II
PSY Connect
Part A
Course Home
H₂C
pt
Draw the major organic product formed when the compound shown below undergoes a reaction with an excess of EtOH under acidic conditions.
Interactive 3D display mode
chem in career
H: 2D EXP
4
Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default.
I UZO
38 o
Review | Constants | Periodic
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I'm not sure how to solve 115. I saw one solution that used the ka to solve it, but I don't understand how to find the ka to use or where they were able to get the ka from with the given information in the problem. So if you could please make this clear in the answer. Thank you for your help.
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E MasteringChemistry: Homewor x
session.masteringchemistry.com/myct/itemView?assignmentProblemID=174343995&offset3Dnext
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☐
5:41 PM Sat Jun 29
kennesaw.view.usg.edu
Name:
Lab Section (Day & Time):
3361L
Molecular Modeling and Stereochemistry Worksheet
CHEM
Ground Rules:
1. You are required to build models for various tasks presented in this exercise. Molecular modeling programs are not
a substitute for 3-D hand-held molecular models.
2. You will be prompted to include a snapshot of your model with each task at the end of this worksheet. Read the
question carefully to construct and orient the models appropriately. Use your smartphone to take a picture of the
model you build, and insert it at the end of the handout with corresponding prompts. You will not get any credit for
this assignment without correct snapshots of the models you build.
3. Hand-write your responses for each task and insert the snapshots for various models at the end of this docuent. Save
the entire assignment as a single PDF. A consolidated PDF of the completed assignment (including relevant snapshots
of your models should be submitted…
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Dangerous Paint Stripper Jessica has a summer job working for the
city parks program. She has been using a cleaner called “Graffiti Gone” to
remove graffiti from the bathrooms. She has to take a lot of breaks, because
the chemical makes her throat burn. It also makes her feel dizzy sometimes,
especially when the bathrooms don’t have very many windows. On the label, she
sees that the cleaner has methylene chloride in it. She feels like she’s
managing to get the work done, but she is worried about feeling dizzy. She
wants to find out more about this chemical, what harm it can cause, and
whether there are safer ways to do this work.
Questions for following story.
1. What went right in this situation?
2. What went wrong in this situation?
3. What steps should be taken in this workplace to make sure employees are
better protected and prepared the next time?
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