Organic Chemistry (8th Edition)
Organic Chemistry (8th Edition)
8th Edition
ISBN: 9780134042282
Author: Paula Yurkanis 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
Draw and show the full mechanism of how the molecule ((1E, 3E, 5E)-1-methoxyhepta-1,3,5-triene) is built using substitution and elimination reactions. You can start with an alkane of any carbon length with any number of leaving groups attached or with a alkoxide of any carbon length (conjugate base of an alcohol). Show each step and and explanation for each reaction. Also include why the reagents and solvents were picked and what other products can be expected.
Don't USE AI
Don't USE AI

Chapter 8 Solutions

Organic Chemistry (8th Edition)

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
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY