![Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th Edition)](https://compass-isbn-assets.s3.amazonaws.com/isbn_cover_images/9780134240152/9780134240152_smallCoverImage.gif)
Concept explainers
(a)
Interpretation:
The products for the given reaction should be identified.
Concept Introduction:
Nucleophilic acyl substitution:
The carbonyl group of a
(b)
Interpretation:
The products for the given reaction should be identified.
Concept Introduction:
Reaction for aldehydes and ketones in presence of primary
The carbonyl group of a carboxylic acid or carboxylic acid derivative gets converted into imine in presence of primary amine which is depicted as follows,
(c)
Interpretation:
The products for the given reaction should be identified.
Concept Introduction:
The ketone which is carboxylic acid derivative in presence of
(d)
Interpretation:
The product for the given reaction should be identified.
Concept Introduction:
The carbonyl group of a carboxylic acid or carboxylic acid derivative is attached to a group that can be replaced with another group. Therefore, aldehyde and ketone undergoes nucleophilic acyl substitution reactions.
Generally reduction of aldehyde gives primary alcohol and reduction of ketone gives secondary alcohol.
(e)
Interpretation:
The product for the given reaction should be identified.
Concept Introduction:
Nucleophilic acyl substitution:
The carbonyl group of a carboxylic acid or carboxylic acid derivative is attached to a group that can be replaced with another group. Therefore, aldehyde and ketone undergoes nucleophilic acyl substitution reactions.
Generally reduction of aldehyde gives primary alcohol and reduction of ketone gives secondary alcohol.
(f)
Interpretation:
The product for the given reaction should be identified.
Concept Introduction:
Nucleophilic acyl substitution:
The carbonyl group of a carboxylic acid or carboxylic acid derivative is attached to a group that can be replaced with another group. Therefore, aldehyde and ketone undergoes nucleophilic acyl substitution reactions.
The carboxylic acid derivatives namely aldehyde and ketones generally gets protected from converted to acetals in presence of
(g)
Interpretation:
The product for the given reaction should be identified.
Concept Introduction:
Nucleophilic acyl substitution:
The carbonyl group of a carboxylic acid or carboxylic acid derivative is attached to a group that can be replaced with another group. Therefore, aldehyde and ketone undergoes nucleophilic acyl substitution reactions.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 17 Solutions
Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th Edition)
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)