The manner of ring closure-conrotatory or disrotatory- for both thermal and photochemical cyclization of (2E,4Z,6Z,8Z)-2,4,6,8-decatetraene indicating the stereochemistry of the product is to be stated. Concept introduction: An electrocyclic reaction involves the cyclization of a conjugated acyclic system. These reactions are reversible and are highly stereospecific. In elecrocyclic reactions involving even number of electron pairs, a thermal reaction occurs in conrotatory manner and a photochemical reaction occurs in disrotatory manner. In elecrocyclic reactions involving odd number of electron pairs, a thermal reaction occurs in disrotatory manner and a photochemical reaction occurs in conrotatory manner. To predict: The manner of ring closure-conrotatory or disrotatory- for both thermal and photochemical cyclization of (2E,4Z,6Z,8Z)-2,4,6,8-decatetraene. To state: The stereochemistry of the product.

Question

b) Certain cyclic compounds are known to be conformationally similar to carbohydrates, although they are not themselves carbohydrates. One example is Compound C shown below, which could be imagined as adopting four possible conformations. In reality, however, only one of these is particularly stable. Circle the conformation you expect to be the most stable, and provide an explanation to justify your choice. For your explanation to be both convincing and correct, it must contain not only words, but also "cartoon" orbital drawings contrasting the four structures. Compound C Possible conformations (circle one): Дет

Answer 1

Question

Chapter 30.SE, Problem 23AP

Interpretation Introduction

Interpretation:

The manner of ring closure-conrotatory or disrotatory- for both thermal and photochemical cyclization of (2E,4Z,6Z,8Z)-2,4,6,8-decatetraene indicating the stereochemistry of the product is to be stated.

Concept introduction:

An electrocyclic reaction involves the cyclization of a conjugated acyclic system. These reactions are reversible and are highly stereospecific.

In elecrocyclic reactions involving even number of electron pairs, a thermal reaction occurs in conrotatory manner and a photochemical reaction occurs in disrotatory manner.

In elecrocyclic reactions involving odd number of electron pairs, a thermal reaction occurs in disrotatory manner and a photochemical reaction occurs in conrotatory manner.

To predict:

The manner of ring closure-conrotatory or disrotatory- for both thermal and photochemical cyclization of (2E,4Z,6Z,8Z)-2,4,6,8-decatetraene.

To state:

The stereochemistry of the product.

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