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.
(EXM 2, PRBLM 3) Here is this problem, can you explain it to me and show how its done. Thank you I need to see the work for like prbl solving.
can someone draw out the reaction mechanism for this reaction showing all bonds, intermediates and side products
Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided below
What would be the best choices for the missing reagents 1 and 3 in this synthesis?
1. PPh3
3
2. n-BuLi
• Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like.
• Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is.
• Note: if one of your reagents needs to contain a halogen, use bromine.
Click and drag to start drawing a structure.
Chapter 9 Solutions
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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