Indicate the CORRECT alternative: a) Acid halides react only in the presence of a catalyst. b) The reaction of an acid chloride with an alcohol produces less of an ester than using the Fischer reaction. c) The nucleophilic substitution reaction in acid derivatives occurs through an SN1 mechanism. d) Reduction of an ester with LiAlH4 yields only secondary alcohols. e) Hydrolysis of an amide in an acid medium produces a carboxylic acid and a protonated amine.
Indicate the CORRECT alternative: a) Acid halides react only in the presence of a catalyst. b) The reaction of an acid chloride with an alcohol produces less of an ester than using the Fischer reaction. c) The nucleophilic substitution reaction in acid derivatives occurs through an SN1 mechanism. d) Reduction of an ester with LiAlH4 yields only secondary alcohols. e) Hydrolysis of an amide in an acid medium produces a carboxylic acid and a protonated amine.
Chemistry & Chemical Reactivity
10th Edition
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Chapter23: Carbon: Not Just Another Element
Section: Chapter Questions
Problem 106IL
Related questions
Question
Indicate the CORRECT alternative:
a) Acid halides react only in the presence of a catalyst.
b) The reaction of an acid chloride with an alcohol produces less of an ester than using the Fischer reaction.
c) The nucleophilic substitution reaction in acid derivatives occurs through an SN1 mechanism.
d) Reduction of an ester with LiAlH4 yields only secondary alcohols.
e) Hydrolysis of an amide in an acid medium produces a
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by step
Solved in 3 steps with 1 images
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.Recommended textbooks for you
Chemistry & Chemical Reactivity
Chemistry
ISBN:
9781337399074
Author:
John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:
Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:
9781133949640
Author:
John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:
Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:
9781337399074
Author:
John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:
Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:
9781133949640
Author:
John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:
Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning