EBK ORGANIC CHEMISTRY AS A SECOND LANGU
4th Edition
ISBN: 8220102737037
Author: Klein
Publisher: YUZU
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Question
Chapter 7.7, Problem 7.59P
Interpretation Introduction
Interpretation:
Efficient synthesis has to be proposed for the given transformation.
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1. Starting with the molecules shown below, perform three different sequential synthetic steps, showing
the reagent (above the arrow) and the product (after the arrow) for each step. You may use any other
molecules or reagents that you desire. Note that each reaction must be performed on the product of the
prior step, and each product must be a stable, neutral, organic molecule. Work-up / protonation of
anions / addition of water does NOT count as a reaction step (but you are welcome to show it). You are
allowed to use more than one reagent in step, but if you do, the sequence of use must be numbered. If
Example:
1) CH3MgBr
OH
РСС
1) LDA
H.
2) H20
CH2CI2
2) EtCI
Complete:
HO
Provide a synthetic approach for the following reactions. Make sure to do the
retrosynthetic analysis and then provide the forward reaction sequence.
HO
OH
حمام
HO
OH
محمده
HO
Perform the following syntheses. Use the retrosynthetic analysis shown in the example. Be
certain to show all of your reasoning which leads to your final answer. Both can be accomplished
in 2-3 steps. Show all reagents and intermediate products. All reactions necessary to complete
these syntheses can be found in Chapters 6, 7, and 9. Also, look at the reactions in Part I.
Remember, start from the target product and go one-step back to get started.
CI
HC=C
Chapter 7 Solutions
EBK ORGANIC CHEMISTRY AS A SECOND LANGU
Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Predict the major product in each of the following...Ch. 7.3 - Predict the major product in each of the following...Ch. 7.3 - Predict the major product in each of the following...Ch. 7.3 - Predict the major product in each of the following...Ch. 7.3 - Predict the major product in each of the following...
Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.4 - Predict the major products for each of the...Ch. 7.4 - Predict the major products for each of the...Ch. 7.4 - Predict the major products for each of the...Ch. 7.5 - Prob. 7.23PCh. 7.5 - Identify the reagents you would use to make each...Ch. 7.5 - Identify the reagents you would use to make each...Ch. 7.5 - Identify the reagents you would use to make each...Ch. 7.5 - Identify the reagents you would use to make each...Ch. 7.5 - In the space provided, draw a mechanism for each...Ch. 7.5 - In the space provided, draw a mechanism for each...Ch. 7.5 - Prob. 7.33PCh. 7.5 - Prob. 7.34PCh. 7.5 - Prob. 7.35PCh. 7.5 - Prob. 7.36PCh. 7.6 - Based on everything we have just seen, propose a...Ch. 7.6 - Prob. 7.39PCh. 7.6 - Prob. 7.40PCh. 7.6 - Prob. 7.41PCh. 7.6 - Propose a mechanism for the following reaction:Ch. 7.6 - Prob. 7.44PCh. 7.6 - Prob. 7.45PCh. 7.6 - Prob. 7.46PCh. 7.7 - Prob. 7.48PCh. 7.7 - Prob. 7.49PCh. 7.7 - Prob. 7.50PCh. 7.7 - Prob. 7.51PCh. 7.7 - Prob. 7.52PCh. 7.7 - Prob. 7.53PCh. 7.7 - Prob. 7.55PCh. 7.7 - Prob. 7.56PCh. 7.7 - Prob. 7.57PCh. 7.7 - Prob. 7.58PCh. 7.7 - Prob. 7.59PCh. 7.7 - Prob. 7.60PCh. 7.7 - Prob. 7.61PCh. 7.7 - Prob. 7.62PCh. 7.7 - Prob. 7.63PCh. 7.7 - Prob. 7.64PCh. 7.7 - Prob. 7.65P
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- Design a synthesis for the following compound.arrow_forwardPlease help with explanation need.arrow_forward6. Provide a sequence of reactions needed to achieve the transformation shown below. You may use any inorganic reagents and any organic reagents used must contain less than or equal to 2 carbons. Make sure to include intermediates! ?arrow_forward
- I need help and chegg might have the wrong answer I need help with Barrow_forwardPropose an efficient synthesis for the following transformation. 人一 The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagent(s) in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A t-BUOK D H₂SO4 H₂O, Hg504 G HBr B 1) 03:2) DMS E H₂. Lindlar's cat. H HBr, ROOR C Br₂, hv F HCECNa 1 1) R₂BH; 2) H₂O₂, NaOHarrow_forwardChemistry Perform the following syntheses. Use the retrosynthetic analysis shown in the example. Be certain to show all of your reasoning which leads to your final answer. All can be accomplished in 2-3 steps. Show all reagents and intermediate products. All reactions necessary to complete these syntheses can be found in Chapters 6, 7, and 9. Also, look at the reactions in Part I. Remember, start from the target product and go one-step back to get started. HO CH3 Br <- HC EC-arrow_forward
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