Connect Access Card For Organic Chemistry
Connect Access Card For Organic Chemistry
4th Edition
ISBN: 9780077479794
Author: Smith Dr., Janice Gorzynski
Publisher: McGraw-Hill Education
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Chapter 27, Problem 27.17P
Interpretation Introduction

(a)

Interpretation: The stereochemical pathway for the given cycloaddition [6+4] photochemical reaction is to be stated using the Woodward-Hoffmann rules.

Concept introduction: The Diels-Alder reactions are the chemical reactions in which diene and dienophile participate to form Diels-Alder adduct. The diene compounds should be conjugated. Conjugated compounds contain at least one single bond in between two double bonds.

Interpretation Introduction

(b)

Interpretation: The stereochemical pathway for the given cycloaddition [8+2] thermal reaction is to be stated using the Woodward-Hoffmann rules.

Concept introduction: The Diels-Alder reactions are the chemical reactions in which diene and dienophile participate to form Diels-Alder adduct. The diene compounds should be conjugated. Conjugated compounds contain at least one single bond in between two double bonds.

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a) What product is formed from the [1,7] sigmatropic rearrangement of a deuterium in the following triene? (b) Does this reaction proceed in a suprafacial or antarafacial manner under thermal conditions? (c) Does this reaction proceed in a suprafacial or antarafacial manner under photochemical conditions?
Using the Woodward–Hoffmann rules, predict the stereochemistry of belowreaction.   a [6 + 4] thermal cycloaddition
Using the Woodward–Hoffmann rules, predict the stereochemistry of eachreaction.a. a [6 + 4] thermal cycloadditionb. photochemical electrocyclic ring closure of deca-1,3,5,7,9-pentaenec. a [4 + 4] photochemical cycloadditiond. a thermal [5,5] sigmatropic rearrangement

Chapter 27 Solutions

Connect Access Card For Organic Chemistry

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