Fundamentals of General, Organic, and Biological Chemistry, Books a la Carte Plus Mastering Chemistry with Pearson eText -- Access Card Package (8th Edition)
8th Edition
ISBN: 9780134261256
Author: John McMurray, David S. Ballantine, Carl A. Hoeger, Virginia E. Peterson
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 15, Problem 15.52CP
Interpretation Introduction
Interpretation:
Concept Introduction:
Oxidation and Reduction: The several organic molecules oxidation is a process by which a carbon atom gains to more electronegative elements most commonly oxygen, the reduction process by which a carbon atom gains bonds to less electronegative elements.
The alcohol molecule can be oxidized to aldehyde (or) ketones, while carbonyl compound (alcohol, ketone) can be reduced to an alcohols, it is called
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Galactose can exist as a cyclic hemiacetal because one of the alcohol groups reacts with the aldehyde.
1 2 3
4
он он о Н Он Он о
CH2-CH-CH-CH-CH-C-H
6.
CH2-OH
OH C
он
10
он
C
8.
H.
H.
OH
Which carbon atom of the cyclic hemiacetal was originally a part of the aldehyde group?
Carbon:
Which alcohol group in the open-chain structure became a part of the cyclic hemiacetal?
Alcohol:
Which of the following terms correctly describes the relationship between D-fructose and L-fructose?
O epimers
diastereomers
O enantiomers
O cis-trans isomers
The reaction of methoxy benzene with hydrogen iodide will yield a phenol and an alkyl halide. Which of following choices is the correct combination of the products?
Chapter 15 Solutions
Fundamentals of General, Organic, and Biological Chemistry, Books a la Carte Plus Mastering Chemistry with Pearson eText -- Access Card Package (8th Edition)
Ch. 15.1 - Prob. 15.1PCh. 15.1 - Prob. 15.2PCh. 15.2 - Draw structures corresponding to the following...Ch. 15.2 - Prob. 15.1CIAPCh. 15.2 - Prob. 15.2CIAPCh. 15.2 - Prob. 15.4PCh. 15.2 - Draw the line structures and provide common names...Ch. 15.2 - Prob. 15.6KCPCh. 15.3 - For each compound shown next (ad), indicate...Ch. 15.3 - Prob. 15.8KCP
Ch. 15.4 - Prob. 15.9KCPCh. 15.5 - Indicate whether the following compounds will give...Ch. 15.6 - Draw line structures of the following compounds...Ch. 15.6 - Prob. 15.12PCh. 15.7 - Prob. 15.13PCh. 15.7 - Prob. 15.14PCh. 15.7 - Prob. 15.15PCh. 15.7 - Draw the structure of each acetal or ketal final...Ch. 15.7 - Prob. 15.17PCh. 15.7 - Prob. 15.18PCh. 15.7 - Prob. 15.19PCh. 15.7 - Prob. 15.1MRPCh. 15.7 - Prob. 15.2MRPCh. 15.7 - Prob. 15.3MRPCh. 15.7 - Prob. 15.3CIAPCh. 15.7 - (a) What are mirotubules? (b) Why would drugs that...Ch. 15.7 - Tetrodotoxin, found in the puffer fish, has been...Ch. 15 - Prob. 15.20UKCCh. 15 - Prob. 15.21UKCCh. 15 - Prob. 15.22UKCCh. 15 - Prob. 15.23UKCCh. 15 - Prob. 15.24UKCCh. 15 - Prob. 15.25UKCCh. 15 - ALDEHYDESAND KETONES (SECTIONS 15.1 AND 15.2)...Ch. 15 - Draw a structure for a compound that meets each of...Ch. 15 - Prob. 15.28APCh. 15 - Prob. 15.29APCh. 15 - Draw structures corresponding to the following...Ch. 15 - Draw structures corresponding to the following...Ch. 15 - Prob. 15.32APCh. 15 - Prob. 15.33APCh. 15 - The following names are incorrect. What is wrong...Ch. 15 - Prob. 15.35APCh. 15 - Prob. 15.36APCh. 15 - Prob. 15.37APCh. 15 - Prob. 15.38APCh. 15 - Prob. 15.39APCh. 15 - Prob. 15.40APCh. 15 - Draw the structures of the aldehydes that might be...Ch. 15 - Write the structures of the hemiacetal or...Ch. 15 - Write the structures of the hemiacetal or...Ch. 15 - Prob. 15.44APCh. 15 - Prob. 15.45APCh. 15 - Prob. 15.46APCh. 15 - Prob. 15.47APCh. 15 - Prob. 15.48APCh. 15 - Prob. 15.49APCh. 15 - Prob. 15.50CPCh. 15 - Prob. 15.51CPCh. 15 - Prob. 15.52CPCh. 15 - Prob. 15.53CPCh. 15 - Prob. 15.54CPCh. 15 - Name the following compounds: (a) (b) (c) (be sure...Ch. 15 - Draw the structural formulas of the following...Ch. 15 - Prob. 15.57CPCh. 15 - Complete the following equations (refer to Summary...Ch. 15 - Prob. 15.59CPCh. 15 - How could you differentiate between 3-hexanol and...Ch. 15 - The liquids 1-butanol and butanal have similar...Ch. 15 - Prob. 15.62CPCh. 15 - Prob. 15.63GPCh. 15 - Prob. 15.64GPCh. 15 - Using the ketone structural form of fructose...Ch. 15 - Prob. 15.66GP
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biochemistry and related others by exploring similar questions and additional content below.Similar questions
- Which of the following molecular formulas would be for an aldopentose? C4H8O4 C₂H₁408 C6H12O6 C5H1005 Darrow_forwardWhich of the following is true of glucitol? It exists as both ring and open-chain structures with the open-chain structure predominating. It exists only as an open-chain structure. It exists as both ring and open-chain structures with the ring structure predominating. It exists only as a ring structure.arrow_forwardExplain why some carbohydrates turn blue with iodine and some do not. Be specific regarding the chemistry. What is it that is responsible for the change.arrow_forward
- Which of the following is least soluble in hexane? * COOH A^ А B с E D FM COOH COOH COOH COOH 1 p COOHarrow_forwardWhat type of hydrocarbons are their structures? Please describe their stability and chemical reactivity. Fumaric Acid, Capric Acid, Lauric Acid, Myristic Acid, Naphthalene, Diphenyl, Decane, Eicosane, alpha-D-Galactose, alpha-D-Glucose, beta-D-Fructose, and Sucrose.arrow_forwardIdentify the D,L convention of the following monosaccharidesarrow_forward
- The molecule glutaraldehyde is properly described as : a five carbon chain with a ketone group on each end a five carbon chain with a ketone functional group in the middle a five carbon chain with an aldehyde group on each end a six carbon chain with and aldehyde group on each endarrow_forwardPlease note the image question below. CH₂OH ç-o CH₂OPO Dihydroxyacetone phosphate triose phosphate isomerase O True O False H HCOH CH₂OPO Glyceraldehyde 3-phosphate This is a change in configuration because isomers can only be interconverted by temporarily breaking covalent bonds.arrow_forwardWhich of the following monosaccharides structural relationship is CORRECT? * CHO CHO CHO но- H- HO -- но -H- но -OH- H- но -- H- H- H- OH но- -H- ČH2OH ČH,OH CH,OH 1 3 1 and 2 are enantiomers, while 2 and 3 are diastereomers 1 and 2 are diastereomers, while 2 and 3 are diastereomers 1 and 2 are enantiomers, while 2 and 3 are enantiomers O 1 and 2 are diastereomers, while 2 and 3 are enantiomersarrow_forward
- Which of the following disaccharides below is not a reducing sugar?arrow_forwardWhich of the following is true about the waxes? incorporate terpenes as part of their structures formed by an amide bond between a fatty acid and sphingosine structures include two fatty acids linked to glycerol made of a ceramide with additional chemical groups attached formed by an ester bond between a fatty acid and a long-chain alcohol a)arrow_forwardSorbitol is a sweetener often substituted for cane sugar, because it is better tolerated by diabetics. It is also an intermediate in the commercial synthesis of vitamin C. Sorbitol is prepared by high-pressure hydrogenation of glucose over a nickel catalyst. What is the structure (including stereochemistry) of sorbitol?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Biology Today and Tomorrow without Physiology (Mi...BiologyISBN:9781305117396Author:Cecie Starr, Christine Evers, Lisa StarrPublisher:Cengage Learning
Biology Today and Tomorrow without Physiology (Mi...
Biology
ISBN:9781305117396
Author:Cecie Starr, Christine Evers, Lisa Starr
Publisher:Cengage Learning
Macromolecules | Classes and Functions; Author: 2 Minute Classroom;https://www.youtube.com/watch?v=V5hhrDFo8Vk;License: Standard youtube license