Student's Study Guide and Solutions Manual for Organic Chemistry
Student's Study Guide and Solutions Manual for Organic Chemistry
8th Edition
ISBN: 9780134066585
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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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.

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Chapter 8 Solutions

Student's Study Guide and Solutions Manual for 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