Synthesis of the molecule is to be shown using an Aldol condensation. Concept introduction: If we see the molecule, we find that it is an α,β- unsaturated carbonyl compound. The molecule is an α,β- unsaturated aldehyde , so it can be the product of dehydrating the β- hydroxy aldehyde. To apply a transform that undoes an aldol addition, we must disconnect the bond between α and β carbons. Because the resulting aldehyde precursors are different from each other, more than one aldol product is possible in the forward direction. To produce the desired product only, we should slowly add the aldehyde with α- hydrogens to a basic solution of the aldehyde without α- hydrogens.

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 18, Problem 18.29P

Interpretation Introduction

Interpretation:

Synthesis of the molecule is to be shown using an Aldol condensation.

Concept introduction:

If we see the molecule, we find that it is an α,β- unsaturated carbonyl compound. The molecule is an α,β- unsaturated aldehyde, so it can be the product of dehydrating the β- hydroxy aldehyde. To apply a transform that undoes an aldol addition, we must disconnect the bond between α and β carbons. Because the resulting aldehyde precursors are different from each other, more than one aldol product is possible in the forward direction. To produce the desired product only, we should slowly add the aldehyde with α- hydrogens to a basic solution of the aldehyde without α- hydrogens.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

EEZE LETCHUP ID Draw the most likely conjugate base resulting from this acid-base reaction. Include all lone pairs. Ignore inorganic byproducts. Drawing く NaOCH2CH3 :0: :0: 狗

Answer

2. Provide a clear arrow-pushing mechanism for the following reactions. Do not skip proton transfers, do not combine steps, and make sure your arrows are clear enough to be interpreted without ambiguity. a. CH3 Ph OEt هد Ph CH3 Hint: the species on the left is an ynolate, which behaves a lot like an enolate.

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 18, Problem 18.29P

Interpretation Introduction

Interpretation:

Synthesis of the molecule is to be shown using an Aldol condensation.

Concept introduction:

If we see the molecule, we find that it is an α,β- unsaturated carbonyl compound. The molecule is an α,β- unsaturated aldehyde, so it can be the product of dehydrating the β- hydroxy aldehyde. To apply a transform that undoes an aldol addition, we must disconnect the bond between α and β carbons. Because the resulting aldehyde precursors are different from each other, more than one aldol product is possible in the forward direction. To produce the desired product only, we should slowly add the aldehyde with α- hydrogens to a basic solution of the aldehyde without α- hydrogens.

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 18, Problem 18.29P

Interpretation Introduction

Interpretation:

Synthesis of the molecule is to be shown using an Aldol condensation.

Concept introduction:

If we see the molecule, we find that it is an α,β- unsaturated carbonyl compound. The molecule is an α,β- unsaturated aldehyde, so it can be the product of dehydrating the β- hydroxy aldehyde. To apply a transform that undoes an aldol addition, we must disconnect the bond between α and β carbons. Because the resulting aldehyde precursors are different from each other, more than one aldol product is possible in the forward direction. To produce the desired product only, we should slowly add the aldehyde with α- hydrogens to a basic solution of the aldehyde without α- hydrogens.

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 18, Problem 18.29P

Interpretation Introduction