Organic Chemistry (6th Edition)
Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
bartleby

Concept explainers

Question
Book Icon
Chapter 20.8, Problem 13P
Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with H2O are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with CH3OH are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with NH3 (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of benzoic anhydride [(C6H5CO)2O] with (CH3)2NH (excess) are to be drawn.

Concept introduction: Anhydrides involve two carbonyl groups. The nucleophilic substitution reaction of anhydride involves the attack of nucleophilic at one carbonyl group, which causes the second carbonyl group to be the part of leaving group.

Blurred answer
Students have asked these similar questions
Comparing Hydration Products Using Two Different Methods Draw the product formed when CH3CH2C=CH is treated with each of the following sets of reagents: (a) H2O, H2SO4, HgSO4; and (b) R2BH, followed by H2O2, HO−.
Draw the product and indicate the stereochemistry when the given alcohol is treated with each reagent: (a) HBr; (b) PBr3; (c) HCI; (d) SOCI, and pyridine.
Draw the organic products formed when 2-bromo-3-pentanone (CH,CH,COCHBrCH3) is treated with each reagent: (a) LizCO3, LiBr, DMF; (b) CH;CH2NH2; (c) CH;SH.
Knowledge Booster
Background pattern image
Chemistry
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
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY