The comparison and the contrasting factors between molecular orbital model and the local electron model and the use of each theory are to be stated and explained. Concept introduction: When the atomic orbitals overlap with each other in the region where density of electrons is high, then molecular orbitals are formed. Overlap of the atomic orbitals determines the efficiency of the interaction between the atomic orbitals. Energy of bonding molecular orbitals is less than the nonbonding molecular orbitals. To determine: The comparison and the contrasting factors between molecular orbital model and the local electron model and the use of each theory.
The comparison and the contrasting factors between molecular orbital model and the local electron model and the use of each theory are to be stated and explained. Concept introduction: When the atomic orbitals overlap with each other in the region where density of electrons is high, then molecular orbitals are formed. Overlap of the atomic orbitals determines the efficiency of the interaction between the atomic orbitals. Energy of bonding molecular orbitals is less than the nonbonding molecular orbitals. To determine: The comparison and the contrasting factors between molecular orbital model and the local electron model and the use of each theory.
Interpretation: The comparison and the contrasting factors between molecular orbital model and the local electron model and the use of each theory are to be stated and explained.
Concept introduction: When the atomic orbitals overlap with each other in the region where density of electrons is high, then molecular orbitals are formed. Overlap of the atomic orbitals determines the efficiency of the interaction between the atomic orbitals.
Energy of bonding molecular orbitals is less than the nonbonding molecular orbitals.
To determine: The comparison and the contrasting factors between molecular orbital model and the local electron model and the use of each theory.
Predict the major organic product(s) of the following reactions. Indicate which of the following mechanisms is in operation: SN1, SN2, E1, or E2.
(c)
(4pts)
Mechanism:
heat
(E1)
CH3OH
+
1.5pts each
_E1 _ (1pt)
Br
CH3OH
(d)
(4pts)
Mechanism:
SN1
(1pt)
(e)
(3pts)
1111 I
H
10
Ill!!
H
LDA
THF (solvent)
Mechanism: E2
(1pt)
NC
(f)
Bri!!!!!
CH3
NaCN
(3pts)
acetone
Mechanism: SN2
(1pt)
(SN1)
-OCH3
OCH3
1.5pts each
2pts for either product
1pt if incorrect
stereochemistry
H
Br
(g)
“,、
(3pts)
H
CH3OH
+21
Mechanism:
SN2
(1pt)
H
CH3
2pts
1pt if incorrect
stereochemistry
H
2pts
1pt if incorrect
stereochemistry
A mixture of butyl acrylate and 4'-chloropropiophenone has been taken for proton NMR analysis. Based on this proton NMR, determine the relative percentage of each compound in the mixture
Chapter 4 Solutions
Bundle: Chemistry: An Atoms First Approach, 2nd, Loose-Leaf + OWLv2, 4 terms (24 months) Printed Access Card
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Quantum Molecular Orbital Theory (PChem Lecture: LCAO and gerade ungerade orbitals); Author: Prof Melko;https://www.youtube.com/watch?v=l59CGEstSGU;License: Standard YouTube License, CC-BY