How to carry out the synthesis shown is to be stated. The stereochemical relationship between the â€“COOCH 3 group attached to the cyclohexane ring and the â€“CHO groups in the product is to be stated. Concept introduction: A diene and an alkene attached to electro withdrawing group are the reactants. Hence Dields alder reaction can take place between the diene and dienophile to give a cyclic adduct. The product contains two aldehyde groups in cis relationship. It is possible by the ozonolysis of a double bond in a ring. To state: How to carry out the synthesis shown and the stereochemical relationship between the â€“COOCH 3 group attached to the cyclohexane ring and the â€“CHO groups in the product.

Question

Want to see the full answer?

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 14.SE, Problem 64AP

Interpretation Introduction

Interpretation:

How to carry out the synthesis shown is to be stated. The stereochemical relationship between the â€“COOCH₃ group attached to the cyclohexane ring and the â€“CHO groups in the product is to be stated.

Concept introduction:

A diene and an alkene attached to electro withdrawing group are the reactants. Hence Dields alder reaction can take place between the diene and dienophile to give a cyclic adduct. The product contains two aldehyde groups in cis relationship. It is possible by the ozonolysis of a double bond in a ring.

To state:

How to carry out the synthesis shown and the stereochemical relationship between the â€“COOCH₃ group attached to the cyclohexane ring and the â€“CHO groups in the product.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

34. Give the expected major product of each of the following reactions. Conc. HI a. CH3CH2CH2OH b. (CH3)2CHCH2CH2OH Conc. HBr H Conc. HI C. OH Conc.HCI d. (CH3CH2)3COH

42. Which of the following halogenated compounds can be used successfully to prepare a Grignard reagent for alcohol synthesis by subsequent reaction with an aldehyde or ketone? Which ones cannot and why? H3C CH3 a. Br H OH b. Cl C. I H H d. Cl e. H OCH3 Br H

For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. ? Will the first MgBr product that forms in this reaction create a new CC bond? olo ? OH جمله O Yes Ⓒ No MgCl ? Will the first product that forms in this reaction create a new CC bond? Click and drag to start drawing a structure. Yes No X ☐ : ☐ टे PH

Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 14.SE, Problem 64AP

Interpretation Introduction

Interpretation:

How to carry out the synthesis shown is to be stated. The stereochemical relationship between the â€“COOCH₃ group attached to the cyclohexane ring and the â€“CHO groups in the product is to be stated.

Concept introduction:

A diene and an alkene attached to electro withdrawing group are the reactants. Hence Dields alder reaction can take place between the diene and dienophile to give a cyclic adduct. The product contains two aldehyde groups in cis relationship. It is possible by the ozonolysis of a double bond in a ring.

To state:

How to carry out the synthesis shown and the stereochemical relationship between the â€“COOCH₃ group attached to the cyclohexane ring and the â€“CHO groups in the product.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 14.SE, Problem 64AP

Interpretation Introduction

Interpretation:

How to carry out the synthesis shown is to be stated. The stereochemical relationship between the â€“COOCH₃ group attached to the cyclohexane ring and the â€“CHO groups in the product is to be stated.

Concept introduction:

A diene and an alkene attached to electro withdrawing group are the reactants. Hence Dields alder reaction can take place between the diene and dienophile to give a cyclic adduct. The product contains two aldehyde groups in cis relationship. It is possible by the ozonolysis of a double bond in a ring.

To state:

How to carry out the synthesis shown and the stereochemical relationship between the â€“COOCH₃ group attached to the cyclohexane ring and the â€“CHO groups in the product.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 14.SE, Problem 64AP

Interpretation Introduction