The hybridisation of central O atom in O3 has to be given; also, the bonding in O 3 in terms of delocalized molecular orbitals has to be described. Concept Introduction: Molecular orbitals are formed by the combination of the atomic orbitals of the atoms in the molecule. The properties of the newly formed molecular orbital will be different from their individual atomic orbitals. In molecular orbital theory, electrons shared by atoms in a molecule reside in the molecular orbitals. Delocalized molecular orbitals are extended over two or more atoms, these are not confined to adjacent bonding atoms. Therefore, the electrons are free to move around the entire molecule. The structures that arise due to delocalization of electrons or charges is called as resonance structures or canonical structures. If a species can be represented in resonance structures, the π bonds of the species are delocalized. To Discuss: The hybridisation of central O atom in O 3 and also the bonding in O 3 in terms of delocalized molecular orbitals.
The hybridisation of central O atom in O3 has to be given; also, the bonding in O 3 in terms of delocalized molecular orbitals has to be described. Concept Introduction: Molecular orbitals are formed by the combination of the atomic orbitals of the atoms in the molecule. The properties of the newly formed molecular orbital will be different from their individual atomic orbitals. In molecular orbital theory, electrons shared by atoms in a molecule reside in the molecular orbitals. Delocalized molecular orbitals are extended over two or more atoms, these are not confined to adjacent bonding atoms. Therefore, the electrons are free to move around the entire molecule. The structures that arise due to delocalization of electrons or charges is called as resonance structures or canonical structures. If a species can be represented in resonance structures, the π bonds of the species are delocalized. To Discuss: The hybridisation of central O atom in O 3 and also the bonding in O 3 in terms of delocalized molecular orbitals.
Solution Summary: The author explains the hybridisation of central O atom in O3 and the bonding in O_
Interpretation: The hybridisation of central O atom in O3 has to be given; also, the bonding in O3 in terms of delocalized molecular orbitals has to be described.
Concept Introduction: Molecular orbitals are formed by the combination of the atomic orbitals of the atoms in the molecule. The properties of the newly formed molecular orbital will be different from their individual atomic orbitals. In molecular orbital theory, electrons shared by atoms in a molecule reside in the molecular orbitals.
Delocalized molecular orbitals are extended over two or more atoms, these are not confined to adjacent bonding atoms. Therefore, the electrons are free to move around the entire molecule.
The structures that arise due to delocalization of electrons or charges is called as resonance structures or canonical structures. If a species can be represented in resonance structures, the π bonds of the species are delocalized.
To Discuss: The hybridisation of central O atom in O3 and also the bonding in O3 in terms of delocalized molecular orbitals.
LTS
Solid:
AT=Te-Ti
Trial 1
Trial 2
Trial 3
Average
ΔΗ
Mass water, g
24.096
23.976
23.975
Moles of solid, mol
0.01763
001767
0101781
Temp. change, °C
2.9°C
11700
2.0°C
Heat of reaction, J
-292.37J -170.473
-193.26J
AH, kJ/mole
16.58K 9.647 kJ 10.85 kr
16.58K59.64701
KJ
mol
12.35k
Minimum AS,
J/mol K
41.582
mol-k
Remember: q = mCsAT (m = mass of water, Cs=4.184J/g°C) & qsin =-qrxn &
Show your calculations for:
AH in J and then in kJ/mole for Trial 1:
qa (24.0969)(4.1845/g) (-2.9°C)=-292.37J
qsin =
qrxn =
292.35 292.37J
AH in J = 292.375 0.2923kJ
0.01763m01
=1.65×107
AH in kJ/mol =
=
16.58K
0.01763mol
mol
qrx
Minimum AS in J/mol K (Hint: use the average initial temperature of the three trials, con
Kelvin.)
AS=AHIT
(1.65×10(9.64×103) + (1.0
Jimai
For the compound: C8H17NO2
Use the following information to come up with a plausible structure:
8
This compound has "carboxylic acid amide" and ether functional groups.
The peaks at 1.2ppm are two signals that are overlapping one another.
One of the two signals is a doublet that represents 6 hydrogens; the
other signal is a quartet that represents 3 hydrogens.
Vnk the elements or compounds in the table below in decreasing order of their boiling points. That is, choose 1 next to the substance with the highest bolling
point, choose 2 next to the substance with the next highest boiling point, and so on.
substance
C
D
chemical symbol,
chemical formula
or Lewis structure.
CH,-N-CH,
CH,
H
H 10: H
C-C-H
H H H
Cale
H 10:
H-C-C-N-CH,
Bri
CH,
boiling point
(C)
Сен
(C) B
(Choose
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INTRODUCTION TO MOLECULAR QUANTUM MECHANICS -Valence bond theory - 1; Author: AGK Chemistry;https://www.youtube.com/watch?v=U8kPBPqDIwM;License: Standard YouTube License, CC-BY