Carbon monoxide ( CO ) is a poisonous compound due to its ability to bind strongly to Fe 2 − in the hemoglobin molecule. The molecular orbitals of ( CO ) have the same energy order as those of the N 2 molecule, (a) Draw a Lewis structure of ( CO ) and assign formal charges. Explain why ( CO ) has a rather small dipole moment of 0.12 D. (b) Compare the bond order of ( CO ) with that from molecular orbital theory. (c) Which of the atoms ( C or O ) is more likely to form bonds with the Fe 2 − ion in hemoglobin?
Carbon monoxide ( CO ) is a poisonous compound due to its ability to bind strongly to Fe 2 − in the hemoglobin molecule. The molecular orbitals of ( CO ) have the same energy order as those of the N 2 molecule, (a) Draw a Lewis structure of ( CO ) and assign formal charges. Explain why ( CO ) has a rather small dipole moment of 0.12 D. (b) Compare the bond order of ( CO ) with that from molecular orbital theory. (c) Which of the atoms ( C or O ) is more likely to form bonds with the Fe 2 − ion in hemoglobin?
Solution Summary: The author explains the Lewis structure along with the formal charges, bond order, and the reason for the small dipole moment of CO.
Carbon monoxide
(
CO
)
is a poisonous compound due to its ability to bind strongly to
Fe
2
−
in the hemoglobin
molecule. The molecular orbitals of
(
CO
)
have the same energy order as those of the N2 molecule, (a) Draw a Lewis structure of
(
CO
)
and assign formal charges. Explain why
(
CO
)
has a rather small dipole moment of 0.12 D. (b) Compare the bond order of
(
CO
)
with that from molecular orbital theory. (c) Which of the atoms
(
C or O
)
is more likely to form bonds with the
Fe
2
−
ion in hemoglobin?
What are the IUPAC Names of all the compounds in the picture?
1) a) Give the dominant Intermolecular Force (IMF) in a sample of each of the following
compounds. Please show your work. (8) SF2, CH,OH, C₂H₂
b) Based on your answers given above, list the compounds in order of their Boiling Point
from low to high. (8)
19.78 Write the products of the following sequences of reactions. Refer to your reaction road-
maps to see how the combined reactions allow you to "navigate" between the different
functional groups. Note that you will need your old Chapters 6-11 and Chapters 15-18
roadmaps along with your new Chapter 19 roadmap for these.
(a)
1. BHS
2. H₂O₂
3. H₂CrO4
4. SOCI₂
(b)
1. Cl₂/hv
2. KOLBU
3. H₂O, catalytic H₂SO4
4. H₂CrO4
Reaction
Roadmap
An alkene 5. EtOH
6.0.5 Equiv. NaOEt/EtOH
7. Mild H₂O
An alkane
1.0
2. (CH3)₂S
3. H₂CrO
(d)
(c)
4. Excess EtOH, catalytic H₂SO
OH
4. Mild H₂O*
5.0.5 Equiv. NaOEt/EtOH
An alkene 6. Mild H₂O*
A carboxylic
acid
7. Mild H₂O*
1. SOC₁₂
2. EtOH
3.0.5 Equiv. NaOEt/E:OH
5.1.0 Equiv. NaOEt
6.
NH₂
(e)
1. 0.5 Equiv. NaOEt/EtOH
2. Mild H₂O*
Br
(f)
i
H
An aldehyde
1. Catalytic NaOE/EtOH
2. H₂O*, heat
3. (CH,CH₂)₂Culi
4. Mild H₂O*
5.1.0 Equiv. LDA
Br
An ester
4. NaOH, H₂O
5. Mild H₂O*
6. Heat
7.
MgBr
8. Mild H₂O*
7. Mild H₂O+
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