For the given each of the electrocyclic reactions, the product formed should be determined. Concept introduction: Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes ( π-system ) , in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring. The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene. The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes ( ring closure ) of the HOMO of conjugated (π-system) polyene. According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions , π-systems Thermal Photochemical 6- π-electrons Disrotatory Conrotatory 8- π-electrons Conrotatory Disrotatory To determine: the major product formed for each of the given electrocyclic reactions.

Question

Want to see the full answer?

Answer 1

Question

Chapter 16, Problem 52PP

(a)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(b)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(c)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(d)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Draw the following molecule: (Z)-1-chloro-1-butene

Identify the molecule as having a(n) E, Z, cis, or trans configuration. CH3 H₁₂C ○ E ○ z ○ cis trans

Identify the molecule as having a(n) E, Z, cis, or trans configuration. H₂C- CH3 О Е ○ cis ○ trans

Answer 2

Question

Chapter 16, Problem 52PP

(a)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(b)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(c)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(d)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 16, Problem 52PP

(a)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(b)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(c)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(d)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 16, Problem 52PP

(a)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(b)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(c)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(d)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 16, Problem 52PP

(a)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(b)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(c)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

(d)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 6

Chapter 16, Problem 52PP

(a)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 7

Chapter 16, Problem 52PP

(a)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 8

(b)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 9

(b)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 10

(c)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 11

(c)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 12

(d)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 13

(d)

Interpretation Introduction

Interpretation:

For the given each of the electrocyclic reactions, the product formed should be determined.

Concept introduction:

Electrocyclic reaction is a concerted cyclization reaction of conjugated polyenes (π-system), in which one π-bond is converted into an σ-bond and remaining π-bonds shift their positions. Thereby the newly formed σ-bond connects the two ends of π-system to form a ring.

The mechanism of the ring formation in the Electrocyclic reaction is drawn by using arrows representing the forming σ-bond and the shifting of π-bonds in the π-system of a polyene.

The reaction conditions (thermal or photochemical) controls the product in such a way that the rotation for end lobes (ring closure) of the HOMO of conjugated (π-system) polyene.

According to Woodward-Hoffmann rule for thermal and photochemical Electrocyclic reactions,

π-systems Thermal Photochemical
6- π-electrons Disrotatory Conrotatory
8- π-electrons Conrotatory Disrotatory

To determine: the major product formed for each of the given electrocyclic reactions.

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 17

Ch. 16.1 - Prob. 1CC Ch. 16.2 - Prob. 2CC Ch. 16.2 - Prob. 3CC Ch. 16.2 - Prob. 4CC Ch. 16.3 - Prob. 5CC Ch. 16.4 - Prob. 1LTS Ch. 16.4 - Prob. 6PTS Ch. 16.4 - Prob. 7PTS Ch. 16.4 - Prob. 8ATS Ch. 16.5 - Prob. 2LTS

π-systems	Thermal	Photochemical
6- π-electrons	Disrotatory	Conrotatory
8- π-electrons	Conrotatory	Disrotatory

Want to see the full answer?

Chapter 16 Solutions