CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY
CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY
8th Edition
ISBN: 2818440043505
Author: Bruice
Publisher: PEARSON
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Chapter 28, Problem 33P
Interpretation Introduction

Interpretation:

The product of the reaction for given two reactants should be drawn.

Concept introduction:

In a sigmatropic reaction “ one new sigma-bond is formed as another breaks.”

CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY, Chapter 28, Problem 33P , additional homework tip  1

Sigma tropic rearrangement reactions are designated with digits. For example a [1, 3] sigma tropic rearrangement describe a reaction in which the residue migrates from position 1 to position 3.

Woodward –Hoffmann rules are the set of rules used to vindicate or predict certain aspects of the stereo chemical outcome and activation energy of pericyclic reactions.

Woodward – Hoffmann rules for sigma tropic rearrangement reactions are listed below

SumofthenumberofbondsinthereactingsytemsofbothreagentsReactionconditionsAllowedmodeofbond formationEvennumberThermalAntarafacialPhotochemicalSuprafacialOddnumberThermalSuprafacialPhotochemicalAntarafacial

Migration of carbon and hydrogen will occur in a sigmatropic rearrangement reaction. Migration of hydrogen in suprafacial and antarafacial rearrangement can be represented as follows,

CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY, Chapter 28, Problem 33P , additional homework tip  2CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY, Chapter 28, Problem 33P , additional homework tip  3

Carbon migrating with one lobe of its p orbital interacting

CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY, Chapter 28, Problem 33P , additional homework tip  4 CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY, Chapter 28, Problem 33P , additional homework tip  5

Carbon migrating with both lobe of its p orbital interacting

CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY, Chapter 28, Problem 33P , additional homework tip  6CHEM 262 ORG CHEM EBOOK DIGITAL DELIVERY, Chapter 28, Problem 33P , additional homework tip  7

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2. Please consider the two all 'cis' isomers of trimethylcyclohexane drawn below. Draw the two chair conformers of each stereoisomer below (1 and 2) and calculate their torsional interaction energies in order to identify the lower energy conformer for each stereoisomer. Based on your calculations, state which of the two stereoisomers 1 and 2 is less stable and which is more stable. [1,3-diaxial CH3 CH3 = 3.7kcal/mol; 1,3-diaxial CH3 H = 0.88kcal/mol; cis-1,2 (axial:equatorial) CH3 CH3 = 0.88kcal/mol; trans-1,2-diequatorial CH3 CH3 = 0.88kcal/mol) all-cis-1,2,3- 1 all-cis-1,2,4- 2
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