1) Propose an efficient synthesis for the following Transformation.**You can only use the reactions/reagents that have been covered in class.2) Propose an efficient synthesis for the following Transformation.**You can only use the reactions/reagents that have been covered in class.**The only source of carbon for this question is ethylene oxide. In case you need strong bulkybase or strong small base for elimination you can use tert-butoxide and methoxide as reagent.Ethylene oxideIs the Only sourceof carbon for thisquestion3) Propose an efficient synthesis for the following Transformation.**You can only use the reactions/reagents that have been covered in class.

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1) Propose an efficient synthesis for the following Transformation. **You can only use the reactions/reagents that have been covered in class.

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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Question

1) Propose an efficient synthesis for the following Transformation.
**You can only use the reactions/reagents that have been covered in class.
2) Propose an efficient synthesis for the following Transformation.
**You can only use the reactions/reagents that have been covered in class.
**The only source of carbon for this question is ethylene oxide. In case you need strong bulky
base or strong small base for elimination you can use tert-butoxide and methoxide as reagent.
Ethylene oxide
Is the Only source
of carbon for this
question
3) Propose an efficient synthesis for the following Transformation.
**You can only use the reactions/reagents that have been covered in class.

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[Review Topics] [References] Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C CH3 H2O NaOH • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Nat, I', in your answer. • In cases where there is more than one answer, just draw one. C opy aste C. Previous Next Email Instructor Save and Ex Cengage Learning | Cengage Technical Support 5:48 PI 82°F 3/28/20
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Draw the major product for the oxidation reaction. Then, draw the proper FULL electron-pushing mechanism for the reaction, including ALL intermediates (with formal charges) and electron-pushing arrows. Label the electrophile and nucleophile in each step.
Please answer completely will give rating surely Both questions answers needed
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Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps.
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Please help with these and include the steps in the reaction so i can better understand how they work! just 1 or two of them is fine
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