(a)
Interpretation:
The structure of alcohol that is required to prepare the given aldehyde has to be drawn.
Concept Introduction:
Carbonyl compounds such as
(b)
Interpretation:
The structure of alcohol that is required to prepare the given ketone has to be drawn.
Concept Introduction:
Carbonyl compounds such as aldehydes and ketones can be synthesized by oxidation or reduction reaction. When a primary alcohol undergoes oxidation reaction, the product obtained is carboxylic acid that is formed through the intermediate aldehyde. When mild oxidizing agent is used, aldehyde can be obtained as product from primary alcohol. When a secondary alcohol undergoes oxidation reaction, the product obtained is a ketone. This cannot be further oxidized. Tertiary alcohols do not undergo oxidation reaction. Some of the mild oxidizing agents used are
(c)
Interpretation:
The structure of alcohol that is required to prepare the given ketone has to be drawn.
Concept Introduction:
Carbonyl compounds such as aldehydes and ketones can be synthesized by oxidation or reduction reaction. When a primary alcohol undergoes oxidation reaction, the product obtained is carboxylic acid that is formed through the intermediate aldehyde. When mild oxidizing agent is used, aldehyde can be obtained as product from primary alcohol. When a secondary alcohol undergoes oxidation reaction, the product obtained is a ketone. This cannot be further oxidized. Tertiary alcohols do not undergo oxidation reaction. Some of the mild oxidizing agents used are
(d)
Interpretation:
The structure of alcohol that is required to prepare the given ketone has to be drawn.
Concept Introduction:
Carbonyl compounds such as aldehydes and ketones can be synthesized by oxidation or reduction reaction. When a primary alcohol undergoes oxidation reaction, the product obtained is carboxylic acid that is formed through the intermediate aldehyde. When mild oxidizing agent is used, aldehyde can be obtained as product from primary alcohol. When a secondary alcohol undergoes oxidation reaction, the product obtained is a ketone. This cannot be further oxidized. Tertiary alcohols do not undergo oxidation reaction. Some of the mild oxidizing agents used are
Want to see the full answer?
Check out a sample textbook solutionChapter 15 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- Give the structure of an alcohol that could be used to prepare each of the following compounds: a. b. c.arrow_forwardExplain the characteristic reaction of aldehydes and ketones ?arrow_forward1. What is the role of the acetic acid in the oxidation of Cyclohexanol to Cyclohexanone? Write the balanced chemical reaction between acetic acid and sodium hypochlorite.2. How do you neutralize the acetic acid regenerated in the reaction? Write the balanced chemical reaction.arrow_forward
- 1. Draw the structural formula of the hemiacetal formed from each ơf the following pairs of reactants. a. Acetaldehyde and methanol 0 b. 2-Pentanone and ethyl alcohol С. Butanal and isopropyl alcohol d. Acetone and ethanolarrow_forward4. The organic starting materials for the preparation of an ester could be C. a ketone and alcohol A an acid and alcohol B. water and oxygen D. alkane and aldehydearrow_forward1. When an aldehyde is reduced with hydrogen (H2) gas in the presence of a transition metal catalyst, what type of product is formed? A. primary alcohol B. secondary alcohol C. tertiary alcohol D. carboxylic acidarrow_forward
- II- Chemical Reactions of Aldehydes and Ketones. 1. Draw the structural formula of the organic product when each of the following aldehydes is oxidized to carboxylic acid. a) Ethanal b) Pentanal c) Formaldehydes d) 3,4-dichlorohexanal 2. What are the characteristics of a positive Tollens test for aldehydes? 3. What is the oxidizing agent in Tollens solution? 4. What are the characteristics of a positive Benedict's test for aldehydes? 5. What is the oxidizing agent in benedict's solution?arrow_forward4. What product forms in the reaction of one carboxylic acid molecule with an alcohol? A. wax B. fatty acid C. phospholipid D. steroid E. glycerolarrow_forwardgive an example of an oxidation reaction with hexanol that will result in an aldehydearrow_forward
- What are the major products of the reaction of ethyl benzoate with hydrochloric acid and water? a. benzoic acid and ethanol b. phenylic acid and ethanol c. ethanoic acid and benzene d. acetic acid and toluene e. phenylic acid and methanolarrow_forward1. Which of the following can be oxidized to produce aldehydes and ketones? A. Alcohols B. Amino Acids C. Carboxylic Acid D. Esterarrow_forward10. Dehydration of glycerin when heated in the presence of potassium hydrogen sulfate leads to the formation of?A) Unsaturated aldehydeB) Unsaturated hydrocarbonB) Unsaturated aldehyde alcoholD) Unsaturated esterarrow_forward
- World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningChemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co