EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
8th Edition
ISBN: 8220102744127
Author: Bruice
Publisher: PEARSON
Question
Book Icon
Chapter 8, Problem 86P

(a)

Interpretation Introduction

Interpretation:

  • The total number of MOs of 1,3,5,7- octatetraene gives has to be predicted.

Concept Introduction:

Molecular orbitals:

Linear combination of atomic orbitals leads to the formation of molecular orbital; the number of molecular orbitals produced are equal to the number of atomic orbitals involved.

Bonding molecular orbital:

Side-to-side overlap of in-phase p-orbitals produces a pi-bonding molecular orbitals and designated as ψ1.

Anti-bonding molecular orbital:

The side-to-side interaction between out-of-phase p-orbitals produces a π* anti-bonding molecular orbital.

(b)

Interpretation Introduction

Interpretation:

  • The total number of bonding and anti-bonding orbitals of 1,3,5,7- octatetraene have  to be predicted.

Concept Introduction:

Molecular orbitals:

Linear combination of atomic orbitals leads to the formation of molecular orbital; the number of molecular orbitals produced are equal to the number of atomic orbitals involved.

Bonding molecular orbital:

Side-to-side overlap of in-phase p-orbitals produces a pi-bonding molecular orbitals and designated as ψ1.

Anti-bonding molecular orbital:

The side-to-side interaction between out-of-phase p-orbitals produces a π* anti-bonding molecular orbital.

(c)

Interpretation Introduction

Interpretation:

  • The symmetric and anti-symmetric molecular orbitals of 1,3,5,7- octatetraene have to be predicted.

Concept Introduction:

Molecular orbitals:

Linear combination of atomic orbitals leads to the formation of molecular orbital; the number of molecular orbitals produced are equal to the number of atomic orbitals involved.

Bonding molecular orbital:

Side-to-side overlap of in-phase p-orbitals produces a pi-bonding molecular orbitals and designated as ψ1.

Anti-bonding molecular orbital:

The side-to-side interaction between out-of-phase p-orbitals produces an π* anti-bonding molecular orbital.

Symmetric molecular orbitals:

The molecular orbitals that possess a internal plane of symmetry is known as symmetric molecular orbitals and the molecular orbitals that does not possess internal plane of symmetry is known as anti-symmetric molecular orbitals.

(d)

Interpretation Introduction

Interpretation:

  • The HOMO and LUMO molecular orbitals of 1,3,5,7- octatetraene in the ground state have to be predicted.

Concept Introduction:

Molecular orbitals:

Linear combination of atomic orbitals leads to the formation of molecular orbital; the number of molecular orbitals produced are equal to the number of atomic orbitals involved.

HOMO (Highest occupied molecular orbital):

The accommodation of electrons at the highest-energy molecular orbitals is known as HOMO.

LUMO:

The lowest-energy of molecular orbitals that do not contain electrons is known as LUMO.

(e)

Interpretation Introduction

Interpretation:

  • The HOMO and LUMO molecular orbitals of 1,3,5,7- octatetraene in the excited state have to be predicted.

Concept Introduction:

Molecular orbitals:

Linear combination of atomic orbitals leads to the formation of molecular orbital; the number of molecular orbitals produced are equal to the number of atomic orbitals involved.

HOMO (Highest occupied molecular orbital):

The accommodation of electrons at the highest-energy molecular orbitals is known as HOMO.

LUMO:

The lowest-energy of molecular orbitals that do not contain electrons are known as LUMO.

(f)

Interpretation Introduction

Interpretation:

  • The relation between HOMO, LUMO and symmetric and antisymmetric orbitals have to be predicted.

Concept Introduction:

Molecular orbitals:

Linear combination of atomic orbitals leads to the formation of molecular orbital; the number of molecular orbitals produced are equal to the number of atomic orbitals involved.

HOMO (Highest occupied molecular orbital):

The accommodation of electrons at the highest-energy molecular orbitals is known as HOMO.

LUMO:

The lowest-energy of molecular orbitals that do not contain electrons are known as LUMO.

(g)

Interpretation Introduction

Interpretation:

  • The number of nodes present in the highest energy MO has to be predicted.

Concept Introduction:

Molecular orbitals:

Linear combination of atomic orbitals leads to the formation of molecular orbital; the number of molecular orbitals produced are equal to the number of atomic orbitals involved.

HOMO (Highest occupied molecular orbital):

The accommodation of electrons at the highest-energy molecular orbitals is known as HOMO.

LUMO:

The lowest-energy of molecular orbitals that do not contain electrons is known as LUMO.

Node: The absence of electron; which means the probability of electrons is zero.

Blurred answer
Students have asked these similar questions
Answer the following questions for the molecular orbitals (MOs) of 1,3,5,7-octatetraene: a. How many MOs does the compound have? b. Which are the bonding MOs, and which are the antibonding MOs? c. Which MOs are symmetric, and which are antisymmetric? d. Which MO is the HOMO and which is the LUMO in the ground state? e. Which MO is the HOMO and which is the LUMO in the excited state? f. What is the relationship between HOMO and LUMO and symmetric and antisymmetric orbitals? g. How many nodes does the highest-energy MO of 1,3,5,7-octatetraene have between the nuclei?
Answer the following questions for the MOs of 1,3,5-hexatriene: a. Which are bonding MOs, and which are antibonding MOs? b. Which MOs are the HOMO and the LUMO in the ground state? c. Which MOs are the HOMO and the LUMO in the excited state? d. Which MOs are symmetric, and which are antisymmetric? e. What is the relationship between HOMO and LUMO and symmetric and antisymmetric MOs?
7. Provide a MO diagram, which depicts the relative energies of the pi molecular orbitals of Cyclooctatetraene. Label each orbital. Label the HOMO and the LUMO. Show which MOs are filled in Cyclooctatetraene's ground state (A diagram will be sufficient; you do not have to draw the MOS).

Chapter 8 Solutions

EBK ORGANIC CHEMISTRY

Ch. 8.7 - Prob. 12PCh. 8.7 - Prob. 13PCh. 8.8 - Prob. 14PCh. 8.8 - Prob. 15PCh. 8.8 - Prob. 16PCh. 8.9 - Which member of each pair is the stronger acid?Ch. 8.9 - Which member of each pair is the stronger base? a....Ch. 8.9 - Rank the following compounds from strongest acid...Ch. 8.10 - Prob. 20PCh. 8.10 - Which acid in each of the following pairs is...Ch. 8.10 - Prob. 23PCh. 8.11 - Prob. 24PCh. 8.11 - Prob. 26PCh. 8.12 - Prob. 27PCh. 8.12 - Prob. 28PCh. 8.12 - Prob. 29PCh. 8.12 - Prob. 30PCh. 8.12 - Prob. 31PCh. 8.12 - Prob. 32PCh. 8.13 - Prob. 33PCh. 8.13 - Prob. 34PCh. 8.13 - Prob. 35PCh. 8.13 - What are the major 1,2- and 1,4-addition products...Ch. 8.13 - Prob. 38PCh. 8.14 - Prob. 39PCh. 8.14 - Prob. 40PCh. 8.14 - Prob. 41PCh. 8.14 - Prob. 42PCh. 8.14 - Prob. 43PCh. 8.14 - Prob. 44PCh. 8.14 - Prob. 46PCh. 8.15 - Prob. 47PCh. 8.17 - Prob. 48PCh. 8.17 - Prob. 49PCh. 8.18 - Prob. 50PCh. 8.18 - Prob. 52PCh. 8.18 - Prob. 53PCh. 8.18 - Prob. 54PCh. 8.19 - Prob. 55PCh. 8.20 - Prob. 56PCh. 8.20 - What orbitals contain the electrons represented as...Ch. 8.20 - Prob. 59PCh. 8.20 - Prob. 60PCh. 8 - Prob. 61PCh. 8 - Prob. 62PCh. 8 - Prob. 63PCh. 8 - Prob. 64PCh. 8 - Prob. 65PCh. 8 - Prob. 66PCh. 8 - Prob. 67PCh. 8 - Prob. 68PCh. 8 - Prob. 69PCh. 8 - Prob. 70PCh. 8 - Prob. 71PCh. 8 - Prob. 72PCh. 8 - Prob. 73PCh. 8 - Which compound is the strongest base?Ch. 8 - Prob. 75PCh. 8 - Prob. 76PCh. 8 - a. The A ring (Section 3.16) of cortisone (a...Ch. 8 - Prob. 78PCh. 8 - Prob. 79PCh. 8 - Prob. 80PCh. 8 - Prob. 81PCh. 8 - Purine is a heterocyclic compound with four...Ch. 8 - Prob. 83PCh. 8 - Why is the delocalization energy of pyrrole (21...Ch. 8 - Prob. 85PCh. 8 - Prob. 86PCh. 8 - Prob. 87PCh. 8 - A student obtained two products from the reaction...Ch. 8 - Prob. 89PCh. 8 - a. How could each of the following compounds be...Ch. 8 - Draw the products obtained from the reaction of...Ch. 8 - How would the following substituents affect the...Ch. 8 - Prob. 93PCh. 8 - The acid dissociation constant (Ka) for loss of a...Ch. 8 - Protonated cyclohexylamine has a Ka = 1 1011...Ch. 8 - Draw the product or products that would be...Ch. 8 - Prob. 97PCh. 8 - Prob. 98PCh. 8 - Prob. 99PCh. 8 - Prob. 100PCh. 8 - Prob. 101PCh. 8 - a. Propose n mechanism for the following reaction:...Ch. 8 - Prob. 103PCh. 8 - As many as 18 different Diels-Alder products can...Ch. 8 - Prob. 105PCh. 8 - Prob. 106PCh. 8 - Prob. 107PCh. 8 - Prob. 108PCh. 8 - The experiment shown next and discussed in Section...Ch. 8 - Prob. 110PCh. 8 - Prob. 111PCh. 8 - Prob. 112PCh. 8 - Prob. 1PCh. 8 - Prob. 2PCh. 8 - Prob. 3PCh. 8 - Prob. 4PCh. 8 - Prob. 5PCh. 8 - Prob. 6PCh. 8 - Prob. 7PCh. 8 - Prob. 8PCh. 8 - Prob. 9PCh. 8 - Prob. 10PCh. 8 - Prob. 11PCh. 8 - Prob. 12P
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Physical Chemistry
Chemistry
ISBN:9781133958437
Author:Ball, David W. (david Warren), BAER, Tomas
Publisher:Wadsworth Cengage Learning,