Tt B 4. Do ANY THREE of the following four problems, as directed. If you do all four, I will take your best three. I-III) Provide a good complete laboratory synthesis (list of reagents in proper sequence) for the conversions shown (right to left). Use familiar reagents and allowed reactants in known reactions that generate the desired product in good yield. Show product after each reaction. Track carbons carefully - let the last step guide your overall strategy. 1) The ester on the right is your only source of carbon to make the ester on the left. (starting material) ih S 35% ((---)

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
Synthesis 1
Tt 2 0 ₂
4. Do ANY THREE of the following four problems, as directed. If you do all four, I will take your best three.
I-III) Provide a good complete laboratory synthesis (list of reagents in proper sequence) for the conversions shown
(right to left). Use familiar reagents and allowed reactants in known reactions that generate the desired product in
good yield. Show product after each reaction. Track carbons carefully-let the last step guide your overall strategy.
1) The ester on the right is your only source of carbon to make the ester on the left.
(starting material)
5
any alcohols
(starting materials)
II) All alcohols (with MF-CnH2n+20) are your only sources of carbon to make the secondary amine shown.
35%
Transcribed Image Text:Tt 2 0 ₂ 4. Do ANY THREE of the following four problems, as directed. If you do all four, I will take your best three. I-III) Provide a good complete laboratory synthesis (list of reagents in proper sequence) for the conversions shown (right to left). Use familiar reagents and allowed reactants in known reactions that generate the desired product in good yield. Show product after each reaction. Track carbons carefully-let the last step guide your overall strategy. 1) The ester on the right is your only source of carbon to make the ester on the left. (starting material) 5 any alcohols (starting materials) II) All alcohols (with MF-CnH2n+20) are your only sources of carbon to make the secondary amine shown. 35%
Expert Solution
steps

Step by step

Solved in 3 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