Draw the Fischer projection for D − xylitol produced when D − xylose is reduced. Concept introduction: The three- dimensional structure stereoisomers on a plane represents the Fisher projections. In the Fischer projection, a chiral carbon represented as intersection of horizontal and vertical line. The horizontal lines are shown by bonds pointing above the plane and vertical lines as bonds pointing below the plane. In fisher projection, the carbonyl group of aldehyde or ketone always placed on the top of vertical line. D and L classification based on the furthest chiral C from ketone or aldehyde. D: if − O H group of the furthest chiral C is right side of the vertical line L: it − O H group of the furthest chiral C is left side of the vertical line.

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 13.5, Problem 13.37QAP

Interpretation Introduction

Interpretation: Draw the Fischer projection for D− xylitol produced when D− xylose is reduced.

Concept introduction:

The three- dimensional structure stereoisomers on a plane represents the Fisher projections.

In the Fischer projection, a chiral carbon represented as intersection of horizontal and vertical line.

The horizontal lines are shown by bonds pointing above the plane and vertical lines as bonds pointing below the plane.

In fisher projection, the carbonyl group of aldehyde or ketone always placed on the top of vertical line.

D and L classification based on the furthest chiral C from ketone or aldehyde.

D: if −OH group of the furthest chiral C is right side of the vertical line

L: it −OH group of the furthest chiral C is left side of the vertical line.

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 Lewis structure for the polyatomic phosphite (PO¾³¯) a anion. Be sure to include all resonance structures that satisfy the octet rule. C I A [ ]¯

Decide whether these proposed Lewis structures are reasonable. proposed Lewis structure Is the proposed Lewis structure reasonable? Yes. :0: Cl C C1: 0=0: : 0 : : 0 : H C N No, it has the wrong number of valence electrons. The correct number is: ☐ No, it has the right number of valence electrons but doesn't satisfy the octet rule. The symbols of the problem atoms are:* ☐ Yes. No, it has the wrong number of valence electrons. The correct number is: ☐ No, it has the right number of valence electrons but doesn't satisfy the octet rule. The symbols of the problem atoms are:* Yes. ☐ No, it has the wrong number of valence electrons. The correct number is: ☐ No, it has the right number of valence electrons but doesn't satisfy the octet rule. The symbols of the problem atoms are:* | * If two or more atoms of the same element don't satisfy the octet rule, just enter the chemical symbol as many times as necessary. For example, if two oxygen atoms don't satisfy the octet rule, enter "0,0".

Draw the Lewis structure for the polyatomic trisulfide anion. Be sure to include all resonance structures that satisfy the octet rule. с [ ] - G

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 13.5, Problem 13.37QAP

Interpretation Introduction

Interpretation: Draw the Fischer projection for D− xylitol produced when D− xylose is reduced.

Concept introduction:

The three- dimensional structure stereoisomers on a plane represents the Fisher projections.

In the Fischer projection, a chiral carbon represented as intersection of horizontal and vertical line.

The horizontal lines are shown by bonds pointing above the plane and vertical lines as bonds pointing below the plane.

In fisher projection, the carbonyl group of aldehyde or ketone always placed on the top of vertical line.

D and L classification based on the furthest chiral C from ketone or aldehyde.

D: if −OH group of the furthest chiral C is right side of the vertical line

L: it −OH group of the furthest chiral C is left side of the vertical line.

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 13.5, Problem 13.37QAP

Interpretation Introduction

Interpretation: Draw the Fischer projection for D− xylitol produced when D− xylose is reduced.

Concept introduction:

The three- dimensional structure stereoisomers on a plane represents the Fisher projections.

In the Fischer projection, a chiral carbon represented as intersection of horizontal and vertical line.

The horizontal lines are shown by bonds pointing above the plane and vertical lines as bonds pointing below the plane.

In fisher projection, the carbonyl group of aldehyde or ketone always placed on the top of vertical line.

D and L classification based on the furthest chiral C from ketone or aldehyde.

D: if −OH group of the furthest chiral C is right side of the vertical line

L: it −OH group of the furthest chiral C is left side of the vertical line.

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 13.5, Problem 13.37QAP

Interpretation Introduction