The mechanism for the acid catalyzed cyclisation of L-threose to β-L-threofuranose should be drawn. Concept introduction: Hemiacetal are formed for the compound having both hydroxyl group and aldehyde group in acidic condition. The –OH group of compound attacks the carbonyl group of the same compound, thereby a ring is formed by the carbon atoms and oxygen atom of –OH group with incorporating into the ring. Acid catalyzed reaction are followed by the deprotonation of Hydronium ion to water molecule and then protonation of this water molecule will return to Hydronium ion will take place.

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 24.5, Problem 20CC

Interpretation Introduction

Interpretation:

The mechanism for the acid catalyzed cyclisation of L-threose to β-L-threofuranose should be drawn.

Concept introduction:

Hemiacetal are formed for the compound having both hydroxyl group and aldehyde group in acidic condition.

The –OH group of compound attacks the carbonyl group of the same compound, thereby a ring is formed by the carbon atoms and oxygen atom of –OH group with incorporating into the ring.

Acid catalyzed reaction are followed by the deprotonation of Hydronium ion to water molecule and then protonation of this water molecule will return to Hydronium ion will take place.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Where are the chiral centers in this molecule? Also is this compound meso yes or no?

PLEASE HELP! URGENT!

Where are the chiral centers in this molecule? Also is this compound meso yes or no?

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 24.5, Problem 20CC

Interpretation Introduction

Interpretation:

The mechanism for the acid catalyzed cyclisation of L-threose to β-L-threofuranose should be drawn.

Concept introduction:

Hemiacetal are formed for the compound having both hydroxyl group and aldehyde group in acidic condition.

The –OH group of compound attacks the carbonyl group of the same compound, thereby a ring is formed by the carbon atoms and oxygen atom of –OH group with incorporating into the ring.

Acid catalyzed reaction are followed by the deprotonation of Hydronium ion to water molecule and then protonation of this water molecule will return to Hydronium ion will take place.

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 24.5, Problem 20CC

Interpretation Introduction

Interpretation:

The mechanism for the acid catalyzed cyclisation of L-threose to β-L-threofuranose should be drawn.

Concept introduction:

Hemiacetal are formed for the compound having both hydroxyl group and aldehyde group in acidic condition.

The –OH group of compound attacks the carbonyl group of the same compound, thereby a ring is formed by the carbon atoms and oxygen atom of –OH group with incorporating into the ring.

Acid catalyzed reaction are followed by the deprotonation of Hydronium ion to water molecule and then protonation of this water molecule will return to Hydronium ion will take place.

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 24.5, Problem 20CC

Interpretation Introduction