Synthesis 1 I'm unable to transcribe the text as it appears in the image. Let me summarize the content for you:---**Task Selection and Synthesis Challenge**1. **Task Overview:** - You are to complete any three of the four provided synthesis problems. - For each selected problem, provide a comprehensive laboratory synthesis plan. - List all reagents in their proper sequence required for the conversion shown (right to left). - Select familiar reagents that allow reactions in known conditions to achieve the desired product with good yield. - Carefully trace carbon atoms. Let the final step guide your strategy.2. **Ester Synthesis:** - Use the ester on the right as the sole source of carbon for creating the ester on the left.3. **Alcohol Conversion:** - Alcohols with the general formula CₙH₂ₙ₊₂O are the exclusive carbon sources for synthesizing the specified secondary amine.The illustration shows a detailed reaction pathway with organic structures and arrows indicating the transformation sequence from starting materials to the final product.--- This summary conveys the essentials of the tasks, focusing on the strategic planning and carbon tracing in organic synthesis.

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% ((---)

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...

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