The reaction S 8 ( g ) → 4 S 2 ( g ) has Δ H ° = +237 kJ (a) The S 8 molecule has eight sulfur atoms arranged in a ring. What is the hybridization and geometry around each sulfur atom in S 8 ? (b) The average S- S bond dissociation energy is 225 kJ/mol. Using the value of Δ H ° given above, what is the S=S double bond energy in S 2 (g)? (c) Assuming that the bonding in S 2 is similar to the bonding in O 2 , give a molecular orbital description of the bonding in S 2 . Is S 2 likely to be paramagnetic or diamagnetic?
The reaction S 8 ( g ) → 4 S 2 ( g ) has Δ H ° = +237 kJ (a) The S 8 molecule has eight sulfur atoms arranged in a ring. What is the hybridization and geometry around each sulfur atom in S 8 ? (b) The average S- S bond dissociation energy is 225 kJ/mol. Using the value of Δ H ° given above, what is the S=S double bond energy in S 2 (g)? (c) Assuming that the bonding in S 2 is similar to the bonding in O 2 , give a molecular orbital description of the bonding in S 2 . Is S 2 likely to be paramagnetic or diamagnetic?
The reaction
S
8
(
g
)
→
4
S
2
(
g
)
has
Δ
H
°
= +237 kJ
(a) The S8 molecule has eight sulfur atoms arranged in a ring. What is the hybridization and geometry around each sulfur atom in S8?
(b) The average S-S bond dissociation energy is 225 kJ/mol. Using the value of
Δ
H
°
given above, what is the S=S double bond energy in S2(g)?
(c) Assuming that the bonding in S2 is similar to the bonding in O2, give a molecular orbital description of the bonding in S2. Is S2 likely to be paramagnetic or diamagnetic?
Formula Formula Bond dissociation energy (BDE) is the energy required to break a bond, making it an endothermic process. BDE is calculated for a particular bond and therefore consists of fragments such as radicals since it undergoes homolytic bond cleavage. For the homolysis of a X-Y molecule, the energy of bond dissociation is calculated as the difference in the total enthalpy of formation for the reactants and products. X-Y → X + Y BDE = Δ H f X + Δ H f Y – Δ H f X-Y where, ΔHf is the heat of formation.
10.
Stereochemistry. Assign R/S stereochemistry for the chiral center indicated on the
following compound. In order to recieve full credit, you MUST SHOW YOUR WORK!
H₂N
CI
OH
CI
カー
11. () Stereochemistry. Draw all possible stereoisomers of the following compound. Assign
R/S configurations for all stereoisomers and indicate the relationship between each as
enantiomer, diastereomer, or meso.
NH2
H
HNH,
-18
b)
8.
Indicate whether the following carbocation rearrangements are likely to occur
Please explain your rational using 10 words or less
not likely to occur
• The double bond is still in the
Same position
+
Likely
to oc
occur
WHY?
-3
H3C
Brave
Chair Conformers. Draw the chair conformer of the following substituted
cyclohexane. Peform a RING FLIP and indicate the most stable
conformation and briefly explain why using 20 words or less.
CI
2
-cobs ??
MUST INDICATE H -2
-2
Br
EQ
Cl
OR
AT
Br
H&
most stable
WHY?
- 4
CH
12
Conformational Analysis. Draw all 6 conformers (one above each letter) of the
compound below looking down the indicated bond. Write the letter of the
conformer with the HIGHEST and LOWEST in energies on the lines provided.
NOTE: Conformer A MUST be the specific conformer of the structure as drawn below
-4 NOT
HOH
OH
3
Conformer A:
Br
OH
A
Samo
Br H
04
Br
H
H3
CH₂
H
anti
stagere
Br CH
clipsed
H
Brott
H
IV
H
MISSING 2
-2
B
C
D
E
F
X
6
Conformer with HIGHEST ENERGY:
13. (1
structure
LOWEST ENERGY:
Nomenclature. a) Give the systematic (IUPAC) name structure. b) Draw the
corresponding to this name. HINT: Do not forget to indicate stereochemistry
when applicable.
a)
८८
2
"Br
{t༐B,gt)-bemn€-nehpརི་ཚ༐lnoa
Parent name (noname)
4 Bromo
Sub = 2-methylethyl-4 Bromo nonane
b) (3R,4S)-3-chloro-4-ethyl-2,7-dimethyloctane
# -2
-2
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Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell