LL ORG CHEM
LL ORG CHEM
6th Edition
ISBN: 9781264840083
Author: SMITH
Publisher: MCG
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Chapter 25.3, Problem 5P
Interpretation Introduction

(a)

Interpretation: The product formed when the given compound undergoes thermal electrocyclic ring opening or ring closure is to be predicted. The given process is to be labeled as conrotatory or disrotatory. The stereochemistry around tetrahedral stereogenic centers and double bonds is to be indicated.

Concept introduction: Electrocyclic reactions involve the conversion of σ bonds into π bonds or π bonds into σ bonds. These reactions can take place in photochemical as well as thermal conditions. The photochemical and thermal reactions take place in the presence of light and heat respectively.

Curved arrows aid in determining the movement and flow of electrons in the reaction. The electrons that take part in the chemical reactions are shown by the curved arrows.

Interpretation Introduction

(b)

Interpretation: The product formed when the given compound undergoes thermal electrocyclic ring opening or ring closure is to be predicted. The given process is to be labeled as conrotatory or disrotatory. The stereochemistry around tetrahedral stereogenic centers and double bonds is to be indicated.

Concept introduction: Electrocyclic reactions involve the conversion of σ bonds into π bonds or π bonds into σ bonds. These reactions can take place in photochemical and as well as thermal conditions. The photochemical and thermal reactions take place in the presence of light and heat respectively.

Curved arrows aid in determining the movement and flow of electrons in the reaction. The electrons that take part in the chemical reactions are shown by the curved arrows.

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In the box below, specify which of the given compounds are very soluble in polar aprotic solvents. You may select more than one compound. Choose one or more: NaCl NH4Cl CH3CH2CH2CH2CH2CN CH3CH2OH hexan-2-one NaOH CH3SCH3
On the following structure, select all of the atoms that could ACCEPT a hydrogen bond. Ignore possible complications of aromaticity. When selecting be sure to click on the center of the atom.
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