Correct co, Na" NH2 co. Na This is the Gabriel synthesis of primary amines in which a new C-N bond is formed by reaction of an alkyl halide (or equivalent electrophile) with phthalimide anion. The final amine is freed from the intermediate phthalimide derivative by hydrolysis in alkali b For the mechanism step below, draw curved arows to show electron reorganization. Arrow-pushing Instructions "Na iön H-ÖH Submit
Correct co, Na" NH2 co. Na This is the Gabriel synthesis of primary amines in which a new C-N bond is formed by reaction of an alkyl halide (or equivalent electrophile) with phthalimide anion. The final amine is freed from the intermediate phthalimide derivative by hydrolysis in alkali b For the mechanism step below, draw curved arows to show electron reorganization. Arrow-pushing Instructions "Na iön H-ÖH Submit
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
Related questions
Question

Transcribed Image Text:a Draw the organic products with counterions.
You do not have to consider stereochemistry.
Include counter-ions, e.g., Na", I, in your submission, but draw them in their own separate sketcher.
Separate structures with + signs from the drop-down menu.
P
aste
opy
aste
- [F
NH2
Na
Na"
ChemDoodle
+v
ChemDoodle
ChemDoodle
+ v
ChemDoodle
Correct
.CO2 Na*
„NH2
`CO2- Na+
This is the Gabriel synthesis of primary amines in which a new C-N bond is formed by reaction of an alkyl halide (or equivalent electrophile) with phthalimide anion. The final amine is freed from the intermediate phthalimide derivative by hydrolysis in alkali.
b For the mechanism step below, draw curved arrows to show electron reorganization.
Arrow-pushing Instructions
:ö:
:ö:
Na :OH
H-ÖH
Submit
Expert Solution

This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
This is a popular solution!
Trending now
This is a popular solution!
Step by step
Solved in 2 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
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

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