The Haworth projections of α-D-mannopyranose and β-D-mannopyranose has to be drawn. Concept Introduction: The cyclic representation of monosaccharides is known as Haworth projection. The five membered ring is said to be Furanose and six membered ring is said to be Pyranose. The five or six membered cyclic hemiacetals which have planar structure will be lying perpendicular to the plane of the paper. In monosaccharides, the alcohol and carbonyl groups both are present. The two groups react with each other to form cyclic hemiacetals. α − D − m a n n o p y r a n o s e : When the mannose is written in cyclic (Pyranose) form, if the -OH group is located on the side opposite to the –CH 2 OH group, it is said to be α-D-mannopyranose. β − D − m a n n o p y r a n o s e : When the mannose is written in cyclic (Pyranose) form, if the -OH group is located on the same side of the –CH 2 OH group, it is said to be β-D-mannopyranose.

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 25.2, Problem 25.2P

Interpretation Introduction

Interpretation:

The Haworth projections of α-D-mannopyranose and β-D-mannopyranose has to be drawn.

Concept Introduction:

The cyclic representation of monosaccharides is known as Haworth projection. The five membered ring is said to be Furanose and six membered ring is said to be Pyranose. The five or six membered cyclic hemiacetals which have planar structure will be lying perpendicular to the plane of the paper.

In monosaccharides, the alcohol and carbonyl groups both are present. The two groups react with each other to form cyclic hemiacetals.

α−D−mannopyranose: When the mannose is written in cyclic (Pyranose) form, if the -OH group is located on the side opposite to the –CH₂OH group, it is said to be α-D-mannopyranose.

β−D−mannopyranose: When the mannose is written in cyclic (Pyranose) form, if the -OH group is located on the same side of the –CH₂OH group, it is said to be β-D-mannopyranose.

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 Fischer projections (D-isomer) of Arabinose and Mannose. Draw the Haworth projections of α-Arabinose and β-Mannose. Draw the structure of β-D-mannopyranosyl-(2→4)-α-D-arabinofuranoside.

d-Glucose most often exists as a pyranose, but it can also exist as a furanose. Draw the Haworth projection of a-d-glucofuranose.

Draw the Haworth projection for the cyclic structure of d-mannose by laying down theFischer projection

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 25.2, Problem 25.2P

Interpretation Introduction

Interpretation:

The Haworth projections of α-D-mannopyranose and β-D-mannopyranose has to be drawn.

Concept Introduction:

The cyclic representation of monosaccharides is known as Haworth projection. The five membered ring is said to be Furanose and six membered ring is said to be Pyranose. The five or six membered cyclic hemiacetals which have planar structure will be lying perpendicular to the plane of the paper.

In monosaccharides, the alcohol and carbonyl groups both are present. The two groups react with each other to form cyclic hemiacetals.

α−D−mannopyranose: When the mannose is written in cyclic (Pyranose) form, if the -OH group is located on the side opposite to the –CH₂OH group, it is said to be α-D-mannopyranose.

β−D−mannopyranose: When the mannose is written in cyclic (Pyranose) form, if the -OH group is located on the same side of the –CH₂OH group, it is said to be β-D-mannopyranose.

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 25.2, Problem 25.2P

Interpretation Introduction

Interpretation:

The Haworth projections of α-D-mannopyranose and β-D-mannopyranose has to be drawn.

Concept Introduction:

The cyclic representation of monosaccharides is known as Haworth projection. The five membered ring is said to be Furanose and six membered ring is said to be Pyranose. The five or six membered cyclic hemiacetals which have planar structure will be lying perpendicular to the plane of the paper.

In monosaccharides, the alcohol and carbonyl groups both are present. The two groups react with each other to form cyclic hemiacetals.

α−D−mannopyranose: When the mannose is written in cyclic (Pyranose) form, if the -OH group is located on the side opposite to the –CH₂OH group, it is said to be α-D-mannopyranose.

β−D−mannopyranose: When the mannose is written in cyclic (Pyranose) form, if the -OH group is located on the same side of the –CH₂OH group, it is said to be β-D-mannopyranose.

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 25.2, Problem 25.2P

Interpretation Introduction