(a)
Interpretation:
In the given ester, the portion that came from the acid is to be circled. The ester linkage is to be pointed out.
Concept introduction:
Esters are organic compounds which are formed from acids in which one hydroxyl group is replaced by an alkoxy group. Esters are formed by the reaction between a carboxylic group and an alcohol under the presence of a catalyst which supplies a proton.
(b)
Interpretation:
In the given ester, the portion that came from the acid is to be circled. The ester linkage is to be pointed out.
Concept introduction:
Esters are organic compounds which are formed from acids in which one hydroxyl group is replaced by an alkoxy group. Esters are formed by the reaction between a carboxylic group and an alcohol under the presence of a catalyst which supplies a proton.
(c)
Interpretation:
In the given ester, the portion that came from the acid is to be circled. The ester linkage is to be pointed out.
Concept introduction:
Esters are organic compounds which are formed from acids in which one hydroxyl group is replaced by an alkoxy group. Esters are formed by the reaction between a carboxylic group and an alcohol under the presence of a catalyst which supplies a proton.
![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 15 Solutions
Bundle: Chemistry For Today: General, Organic, And Biochemistry, 9th + Owlv2 With Mindtap Reader, 1 Term (6 Months) Printed Access Card
- what is the pentane effect?arrow_forwardWhy are alcoholic solutions used in the hydroxamic acid test for esters?arrow_forwardWhen reacting an acid halide with amines, it is necessary to use at least two moles of the amine because: A) Acid halides are so unreactive that two moles of the attacking nucleophile are needed B) Using one mole of the amine leads to a neutralization reaction between the two reactants C) Excess amine is needed to react with the hydrohalic acid produced D) The second mole of amine is needed for deprotonation.arrow_forward
- Draw the all the reactants and products involved in a condensation reaction between propanoic acid and ethanamine. Make sure to include the catalyst needed and any secondary products that would form.arrow_forwardFormation of Esters. Odor of ester Chemical Equation:arrow_forwardWhat is porphyrin ?arrow_forward
- Briefly explain why NOT ALL hydrolysis of esters produce a sour smellarrow_forwardGive an example of a medical application of aspirin. Why was aspirin modified and patented into its ester acetylsalicylic acid form that we know today?arrow_forward1. Explain the cleaning property of soaps and synthetic detergents based on their emulsifying action. 2. Between soap and synthetic detergent, which is a better cleaning agent in hard water? Explain in 1 – 3 sentences.arrow_forward
- Please explain and draw Lewis structures for a balanced chemical reaction showing the hydrolysis of ethyl acetate with sodium hydroxide.arrow_forwardNow that you have learned about solubility, explain why aspirin crosses a cell membrane as a neutral carboxylic acid rather than an ionic conjugate base ?arrow_forwardWhy are alcoholic solutions (alcoholic NH2OHꞏHCl, alcoholic KOH, alcoholic HCl) used in the hydroxamic acid test for esters?arrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningLiving By Chemistry: First Edition TextbookChemistryISBN:9781559539418Author:Angelica StacyPublisher:MAC HIGHEROrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305960060/9781305960060_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781559539418/9781559539418_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305081079/9781305081079_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285853918/9781285853918_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285869759/9781285869759_smallCoverImage.gif)