The major product for each of the given E2 reactions is needed to be predicted. Concept introduction: In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide. E2 reaction is a bimolecular elimination reaction in which only one step is involved. The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical . If the β-positions are different and the products formed are also different . This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes . The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes . If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer . To predict: the major product for given E2 reactions.

Question

Want to see the full answer?

Answer 1

Question

Chapter 8, Problem 61PP

(a)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(b)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(c)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(d)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

(EXM 2, PRBLM 3) Here is this problem, can you explain it to me and show how its done. Thank you I need to see the work for like prbl solving.

can someone draw out the reaction mechanism for this reaction showing all bonds, intermediates and side products Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided below

What would be the best choices for the missing reagents 1 and 3 in this synthesis? 1. PPh3 3 2. n-BuLi • Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like. • Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is. • Note: if one of your reagents needs to contain a halogen, use bromine. Click and drag to start drawing a structure.

Answer 2

Question

Chapter 8, Problem 61PP

(a)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(b)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(c)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(d)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 8, Problem 61PP

(a)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(b)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(c)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(d)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 8, Problem 61PP

(a)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(b)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(c)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(d)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 8, Problem 61PP

(a)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(b)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(c)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

(d)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Answer 6

Chapter 8, Problem 61PP

(a)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Answer 7

Chapter 8, Problem 61PP

(a)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Answer 8

(b)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Answer 9

(b)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Answer 10

(c)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Answer 11

(c)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Answer 12

(d)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 reactions.

Answer 13

(d)

Interpretation Introduction

Interpretation:

The major product for each of the given E2 reactions is needed to be predicted.

Concept introduction:

In an elimination reaction, alkenes are formed when alkyl halides are treated with bases via eliminating one proton and one halo group of the alkyl halide.

E2 reaction is a bimolecular elimination reaction in which only one step is involved.

The product of the elimination reaction is depends upon the two β-positions of alkyl halide. If the β-positions are identical and the products formed are also identical. If the β-positions are different and the products formed are also different. This means the double bond can form in two different regions so this type of reaction is called regioselective and the products are called as regiochemical outcomes.

The bulkiness of the base controls the regioselectivity in an elimination reaction. The sterically hindered bases form less substituted alkene and non-sterically hindered bases form more substituted alkenes.

If there are two different β-protons at a β-position of alkyl halide, then on the basis of stereoselectivity the trans-isomer is favored over cis-isomer.

To predict: the major product for given E2 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. 8.3 - Prob. 1LTS Ch. 8.3 - Prob. 1PTS Ch. 8.3 - Prob. 2ATS Ch. 8.3 - Prob. 3ATS Ch. 8.3 - Prob. 4CC Ch. 8.4 - Prob. 2LTS Ch. 8.4 - Prob. 5PTS Ch. 8.4 - Prob. 6ATS Ch. 8.5 - Prob. 3LTS Ch. 8.5 - Prob. 7PTS

Want to see the full answer?

Chapter 8 Solutions