Enamines are generally used to give a selective monoalkylation of ketones which can be conducted under mild acidic conditions. Draw the enamine used in this reaction (NOTE the mechanism for enamine formation is NOT required). From the enamine provide a mechanism for the alkylation and hydrolysis to the ketone product. Make sure to show electron flow with arrows for each step (including proton transfer) to receive full credit. Also, clearly label your ketone product. provide mechanism H* Ph Br H20 enamine ketone

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...
icon
Related questions
Question
100%
Enamines are generally used to give a selective monoalkylation of ketones which can be
conducted under mild acidic conditions. Draw the enamine used in this reaction (NOTE the
mechanism for enamine formation is NOT required). From the enamine provide a mechanism
for the alkylation and hydrolysis to the ketone product. Make sure to show electron flow with
arrows for each step (including proton transfer) to receive full credit. Also, clearly label your
ketone product.
provide
mechanism
H*
Ph
Br
H20
enamine
ketone
Transcribed Image Text:Enamines are generally used to give a selective monoalkylation of ketones which can be conducted under mild acidic conditions. Draw the enamine used in this reaction (NOTE the mechanism for enamine formation is NOT required). From the enamine provide a mechanism for the alkylation and hydrolysis to the ketone product. Make sure to show electron flow with arrows for each step (including proton transfer) to receive full credit. Also, clearly label your ketone product. provide mechanism H* Ph Br H20 enamine ketone
Expert Solution
steps

Step by step

Solved in 2 steps with 1 images

Blurred answer
Knowledge Booster
Protection of Groups in Organic Synthesis
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
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY