Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
bartleby

Concept explainers

Question
Book Icon
Chapter 4, Problem 4.25P
Interpretation Introduction

(a)

Interpretation:

The Lewis structure for an aldetetrose is to be drawn.

Concept introduction:

Monosaccharides are called simple sugars, with the number of oxygen atoms same as the number of carbon atoms. The general formula for monosaccharides is CxH2xOx. Monosaccharides are cyclic as well as non-cyclic. In mono-saccharides, if the carbonyl group involves a terminal carbon, then it is an aldose. In mono-saccharides, if the carbonyl group involves an internal carbon, then it is a ketose. Sugars are further distinguished on the basis of their carbon atoms. A tetrose sugar contains four, a pentose contains five, and a hexose contains six carbon atoms respectively.

Expert Solution
Check Mark

Answer to Problem 4.25P

The Lewis structure for an aldetetrose is

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  1

Explanation of Solution

Aldotetrose is a mono-saccharide. The name “aldo” indicates that the carbonyl group must be present at the terminal carbon atom, while the word “tetrose” indicates a chain of four carbon atoms. Thus, aldotetrose is a sugar having an aldehyde group at the terminal carbon atom, and the structure must have four carbon atoms. The general formula for mono-saccharides is CxH2xOx. Thus, the molecular formula for the aldotetrose must be C4H8O4. The structure for aldotetrose is as below:

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  2

The molecular formula for the above structure is C4H8O4. Usually, lone pairs of electrons on the atoms, wherever applicable, are shown in the Lewis structure, but in these molecules, it is not relevant, thus ignored.

Conclusion

Altetrose is a mono-saccharide having a carbonyl group at the terminal carbon atom, and its molecular formula is C4H8O4.

Interpretation Introduction

(b)

Interpretation:

The Lewis structure for a ketotetrose is to be drawn.

Concept introduction:

Monosaccharides are called simple sugars, with the number of oxygen atoms same as the number of carbon atoms. The general formula for a monosaccharide is CxH2xOx. Monosaccharides are cyclic as well as non-cyclic. In mono-saccharides, if the carbonyl group involves a terminal carbon, then it is an aldose. In mono-saccharides, if the carbonyl group involves an internal carbon, then it is a ketose. Sugars are further distinguished on the basis of their carbon atoms. A tetrose sugar contains four, a pentose contains five, and a hexose contains six carbon atoms respectively.

Expert Solution
Check Mark

Answer to Problem 4.25P

The Lewis structure for a ketotetrose is

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  3

Explanation of Solution

Ketotetrose is a type of mono-saccharide. The name “keto” indicates that the carbonyl group must be present at the internal carbon atom, while the word “tetrose” indicates the chain of four carbon atoms. Thus, ketotetrose is a sugar having a carbonyl group at the internal carbon atom, and the structure must have four carbon atoms. The general molecular formula for mono-saccharides is CxH2xOx. Thus, the molecular formula for the ketotetrose must be C4H8O4. The structure for ketotetrose is as below:

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  4

The molecular formula for the above structure is C4H8O4. Usually, lone pairs of electrons on the atoms, wherever applicable, are shown in the Lewis structure, but in these molecules, it is not relevant, thus ignored.

Conclusion

Ketotetrose is a mono-saccharide having a carbonyl group at the internal carbon atom, and its molecular formula is C4H8O4.

Interpretation Introduction

(c)

Interpretation:

The Lewis structure for an aldetriose is to be drawn.

Concept introduction:

Monosaccharides are called simple sugars, with the number of oxygen atoms same as the number of carbon atoms. Thus, the general molecular formula for a monosaccharide is CxH2xOx. Monosaccharides are cyclic as well as non-cyclic. In mono-saccharides, if the carbonyl group involves a terminal carbon, then it is an aldose. In mono-saccharides, if the carbonyl group involves an internal carbon, then it is a ketose. Sugars are further distinguished on the basis of their carbon atoms. A tetrose sugar contains four, a pentose contains five, and a hexose contains six carbon atoms respectively.

Expert Solution
Check Mark

Answer to Problem 4.25P

The Lewis structure for an aldetriose is

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  5

Explanation of Solution

Aldotriose is a type of mono-saccharide. The name “aldo”’ indicates that the carbonyl group must be present at the terminal carbon atom, while the word “triose” indicates a chain of three carbon atoms. Thus, aldotriose is a sugar having an aldehyde group at the terminal carbon atom, and the structure must have three carbon chain. The general molecular formula for mono-saccharides is CxH2xOx. Thus, the molecular formula for the aldotriose must be C3H6O3. The Lewis structure for aldotriose is as below:

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  6

The molecular formula for the above structure is C3H6O3. Usually, lone pairs of electrons on the atoms, wherever applicable, are shown in the Lewis structure, but in these molecules, it is not relevant, thus ignored.

Conclusion

Altetrose is a mono-saccharide having a carbonyl group at the terminal carbon atom, and its molecular formula is C3H6O3.

Interpretation Introduction

(d)

Interpretation:

The Lewis structure for a ketotriose is to be drawn.

Concept introduction:

Monosaccharides are called simple sugars, with the number of oxygen atoms same as the number of carbon atoms. Thus, the general molecular formula for a monosaccharide is CxH2xOx. Monosaccharides are cyclic as well as non-cyclic. In mono-saccharides, if the carbonyl group involves a terminal carbon, then it is an aldose. In mono-saccharides, if the carbonyl group involves an internal carbon, then it is a ketose. Sugars are further distinguished on the basis of their carbon atoms. A tetrose sugar contains four, a pentose contains five, and a hexose contains six carbon atoms respectively.

Expert Solution
Check Mark

Answer to Problem 4.25P

The Lewis structure for a ketotriose is

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  7

Explanation of Solution

Ketotriose is a type of mono-saccharide. The name “keto” indicates that the carbonyl group must be present at the internal carbon atom, while the word “tetrose” indicates the chain of four carbon atoms. Thus, ketotriose is a sugar having a carbonyl group at the internal carbon atom, and the structure must have three carbon atoms. The general molecular formula for mono-saccharides is CxH2xOx. Thus, the molecular formula for the ketotetrose must be C3H6O3. The Lewis structure for ketotriose is as below:

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  8

The molecular formula for the above structure is C3H6O3. Usually, lone pairs of electrons on the atoms, wherever applicable, are shown in the Lewis structure, but in these molecules, it is not relevant, thus ignored.

Conclusion

Ketotetrose is a mono-saccharide having a carbonyl group at the internal carbon atom, and its molecular formula is C3H6O3.

Interpretation Introduction

(e)

Interpretation:

The Lewis structure for a ketohexose, which is different from fructose, is to be drawn.

Concept introduction:

Monosaccharides are called simple sugars, with the number of oxygen atoms same as the number of carbon atoms. Thus, the general molecular formula for a monosaccharide is CxH2xOx. Monosaccharides are cyclic as well as non-cyclic. In mono-saccharides, if the carbonyl group involves a terminal carbon, then it is an aldose. In mono-saccharides, if the carbonyl group involves an internal carbon, then it is a ketose. Sugars are further distinguished on the basis of their carbon atoms. A tetrose sugar contains four, a pentose contains five, and a hexose contains six carbon atoms respectively.

Expert Solution
Check Mark

Answer to Problem 4.25P

The Lewis structure for a ketohexose, which is different from fructose, is

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  9

Explanation of Solution

The Lewis structure for fructose is

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  10

Fructose is a ketohexose with a molecular formula C6H12O6. In the structure above, note that the position of the carbonyl carbon is at one of the internal carbon atoms in the six carbon chain. Another ketohexose, other than fructose, can be drawn by changing the connectivity of any one of the hydroxyl groups attached. Thus, the Lewis structure for a ketohexose, which is different from fructose is

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second), Chapter 4, Problem 4.25P , additional homework tip  11

The molecular formula for the above structure is C6H12O6. Usually, lone pairs of electrons on the atoms, wherever applicable are shown in the Lewis structure, but in these molecules, it is not relevant, thus ignored.

Conclusion

Ketohexose is a mono-saccharide having a carbonyl group at the internal carbon atom, and its molecular formula is C6H12O6.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
(a 4 shows scanning electron microscope (SEM) images of extruded actions of packing bed for two capillary columns of different diameters, al 750 (bottom image) and b) 30-μm-i.d. Both columns are packed with the same stationary phase, spherical particles with 1-um diameter. A) When the columns were prepared, the figure shows that the column with the larger diameter has more packing irregularities. Explain this observation. B) Predict what affect this should have on band broadening and discuss your prediction using the van Deemter terms. C) Does this figure support your explanations in application question 33? Explain why or why not and make any changes in your answers in light of this figure. Figure 4 SEM images of sections of packed columns for a) 750 and b) 30-um-i.d. capillary columns.³
fcrip = ↓ bandwidth Il temp 32. What impact (increase, decrease, or no change) does each of the following conditions have on the individual components of the van Deemter equation and consequently, band broadening? Increase temperature Longer column Using a gas mobile phase instead of liquid Smaller particle stationary phase Multiple Paths Diffusion Mass Transfer
34. Figure 3 shows Van Deemter plots for a solute molecule using different column inner diameters (i.d.). A) Predict whether decreasing the column inner diameters increase or decrease bandwidth. B) Predict which van Deemter equation coefficient (A, B, or C) has the greatest effect on increasing or decreasing bandwidth as a function of i.d. and justify your answer. Figure 3 Van Deemter plots for hydroquinone using different column inner diameters (i.d. in μm). The data was obtained from liquid chromatography experiments using fused-silica capillary columns packed with 1.0-μm particles. 35 20 H(um) 큰 20 15 90 0+ 1500 100 75 550 01 02 594 05 μ(cm/sec) 30 15 10

Chapter 4 Solutions

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)

Ch. 4 - Prob. 4.11PCh. 4 - Prob. 4.12PCh. 4 - Prob. 4.13PCh. 4 - Prob. 4.14PCh. 4 - Prob. 4.15PCh. 4 - Prob. 4.16PCh. 4 - Prob. 4.17PCh. 4 - Prob. 4.18PCh. 4 - Prob. 4.19PCh. 4 - Prob. 4.20PCh. 4 - Prob. 4.21PCh. 4 - Prob. 4.22PCh. 4 - Prob. 4.23PCh. 4 - Prob. 4.24PCh. 4 - Prob. 4.25PCh. 4 - Prob. 4.26PCh. 4 - Prob. 4.27PCh. 4 - Prob. 4.28PCh. 4 - Prob. 4.29PCh. 4 - Prob. 4.30PCh. 4 - Prob. 4.31PCh. 4 - Prob. 4.32PCh. 4 - Prob. 4.33PCh. 4 - Prob. 4.34PCh. 4 - Prob. 4.35PCh. 4 - Prob. 4.36PCh. 4 - Prob. 4.37PCh. 4 - Prob. 4.38PCh. 4 - Prob. 4.39PCh. 4 - Prob. 4.40PCh. 4 - Prob. 4.41PCh. 4 - Prob. 4.42PCh. 4 - Prob. 4.43PCh. 4 - Prob. 4.44PCh. 4 - Prob. 4.45PCh. 4 - Prob. 4.46PCh. 4 - Prob. 4.47PCh. 4 - Prob. 4.48PCh. 4 - Prob. 4.49PCh. 4 - Prob. 4.50PCh. 4 - Prob. 4.51PCh. 4 - Prob. 4.52PCh. 4 - Prob. 4.53PCh. 4 - Prob. 4.54PCh. 4 - Prob. 4.55PCh. 4 - Prob. 4.56PCh. 4 - Prob. 4.57PCh. 4 - Prob. 4.58PCh. 4 - Prob. 4.59PCh. 4 - Prob. 4.60PCh. 4 - Prob. 4.61PCh. 4 - Prob. 4.62PCh. 4 - Prob. 4.63PCh. 4 - Prob. 4.64PCh. 4 - Prob. 4.65PCh. 4 - Prob. 4.66PCh. 4 - Prob. 4.67PCh. 4 - Prob. 4.68PCh. 4 - Prob. 4.69PCh. 4 - Prob. 4.70PCh. 4 - Prob. 4.71PCh. 4 - Prob. 4.72PCh. 4 - Prob. 4.73PCh. 4 - Prob. 4.1YTCh. 4 - Prob. 4.2YTCh. 4 - Prob. 4.3YTCh. 4 - Prob. 4.4YTCh. 4 - Prob. 4.5YTCh. 4 - Prob. 4.6YTCh. 4 - Prob. 4.7YTCh. 4 - Prob. 4.8YTCh. 4 - Prob. 4.9YTCh. 4 - Prob. 4.10YTCh. 4 - Prob. 4.11YTCh. 4 - Prob. 4.12YTCh. 4 - Prob. 4.13YTCh. 4 - Prob. 4.14YTCh. 4 - Prob. 4.15YTCh. 4 - Prob. 4.16YTCh. 4 - Prob. 4.17YTCh. 4 - Prob. 4.18YTCh. 4 - Prob. 4.19YTCh. 4 - Prob. 4.20YTCh. 4 - Prob. 4.21YTCh. 4 - Prob. 4.22YTCh. 4 - Prob. 4.23YTCh. 4 - Prob. 4.24YTCh. 4 - Prob. 4.25YT
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Text book image
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
Text book image
World of Chemistry
Chemistry
ISBN:9780618562763
Author:Steven S. Zumdahl
Publisher:Houghton Mifflin College Div