Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
Question
Book Icon
Chapter 30.4, Problem 4P
Interpretation Introduction

Interpretation:

Product of the photochemical cyclization of (2E,4Z,6E)-2,4,6-octatriene. Of (2E,4Z,6Z)-2,4,6-octatriene.

Concept introduction:

In photochemical reactions, the orbitals of the HOMO of the excited state to determine the course of the reaction. The excited state HOMO has the opposite orientation of the outermost p orbitals compared to the HOMO of the ground state. As a result, the method of ring closure of a photochemical electrocyclic reaction is opposite to that of a thermal electrocyclic reaction for the same number of pie bonds.

Photochemical electrocyclic reactions occur in a conrotatory fashion for a conjugated polyene with an odd number of pie bonds.

Blurred answer
Students have asked these similar questions
The reaction of (2S)-2-chloro-3-methylpentane with sodium iodide yields two products: (2R)-2-iodo-3-methylpentane and racemic 3-iodo-2-methylpentane. Account for the formation of each of these two products. For each product, you should show how it is formed and what that tells you about the mechanism of that specific reaction.
Addition of one mole of HBr to 2,4-hexadiene gives a mixture of 4-bromo2-hexene and 2-bromo-3-hexene. No 5-bromo-2-hexene is formed. Account for the formation of the first two bromoalkenes and for the fact that the third bromoalkene is not formed.
What would the major organic reaction product be from the reaction of 1-bromo-1-methylcyclopentane withsodium hydroxide? Would the elimination reaction outcome be affected if a student accidentally adds sodium tertbutoxide instead of sodium hydroxide?
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning