
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
thumb_up100%
Are
Here is my current understanding:
Carboxylic acids have the ability to donate a hydrogen ion and become deprotonated, therefore it is acidic.
Carboxylate ions are already deprotonated and have already become acidic.
Is this correct?
Expert Solution

This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by stepSolved in 2 steps

Knowledge Booster
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
- Why can an acidic organic compound be separated from a neutral (neither basic nor acidic) organic compound?arrow_forwardPlease helparrow_forwardIf a nonpolar carboxylic acid donates a proton to a base, which of the following results is true? The carboxylic acid becomes a negative ion. The ion is more soluble in water than the original carboxylic acid. The carboxylic acid becomes a positive ion. The ion is more soluble in water than the original carboxylic acid. The carboxylic acid becomes a negative ion. The ion is less soluble in water than the original carboxylic acid. The carboxylic acid becomes a positive ion. The ion is less soluble in water than the original carboxylic acid.arrow_forward
- The purity of the aspirin sample is tested with iron (III) chloride. A purple color resulting from iron (III) chloride test indicates the aspirin sample contains some unreacted salicylic acid and the carboxylic acid group in salicylic acid gives a purple color. the structure of aspirin itself contains a phenolic -OH group. O the aspirin sample contains some unreacted salicylic acid and the phenolic -OH group in salicylic acid gives a purple color. the aspirin sample contains some unreacted salicylic acid and the ring structure in salicylic acid gives a purple color.arrow_forwardWhich one of the following functional groups is a base? aldehyde alcohol carboxylic acid ether aminearrow_forwardDraw a reaction showing the reactants (the ester and water) and the products (the alcohol and the carboxylic acid) for each ester below. You can google the structures of the esters. Ester 1 aspirin, Ester 2 benzocaine, Ester 3 gamma-butyrolactonearrow_forward
- You are given propane and hexanoic acid. Your job is to create the ester isopropyl hexanoate. Use the correct chemical reactions in order to get the products needed to create the ester, assume if there are multiple isomers that you are able to isolate the isomer you need.arrow_forwardWrite the structure of the carboxylic acid that forms when the following aldehyde is oxidized: H3C CHarrow_forwardWhich of the following molecules can be at least 50% deprotonated in water? - alcohol - carboxylic acid - acetyl acetone - acetonearrow_forward
- In an esterification reaction, a carboxylic acid reacts with an excess of alcohol in acidic conditions to form an ester. Draw the structure of the ester product in the reaction between pentanoic acid and 1‑propanol. pentanoic acid+ 1-propanol= ester+ H20 structure of ester product neededarrow_forwardORGANIC FUNCTIONAL GROUPS Understanding the names of carboxylate salts What is the systematic name of the product P of this chemical reaction? HO 0 OH O OH OH + NaOH + H₂Oarrow_forwardOrganic Chemistry Маxwell Draw the organic and inorganic products for the following acid/base reaction. H .N. Н. 2 products H.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- 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

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education

Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning

Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education

Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning

Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY