**Synthetic Pathway Selection Activity**In this exercise, you will choose the correct reagents necessary for each step in a multi-step organic synthesis process.**Instructions:**For each step (I-V) in the synthesis, select the appropriate reagent(s) from the dropdown menu.1. **Correct reagent(s) for Step I** - [ Select ] - Options: - A. PCC/CH2Cl2 - B. Na2Cr2O7/H2SO4/H2O - A or B2. **Correct reagent(s) for Step II** - [ Select ]3. **Correct reagent(s) for Step III** - [ Select ]4. **Correct reagent(s) for Step IV** - [ Select ]5. **Correct reagent(s) for Step V** - [ Select ]**Reaction Diagram Description:**- **Step I:** The starting material is a cyclic alcohol compound. The goal is to transform the alcohol group into an aldehyde.- **Step II:** This involves the conversion of the aldehyde into a different functional group, resulting in a compound with a lactone structure.- **Step III:** The lactone is modified further, preserving the ring structure.- **Step IV:** The compound undergoes a Grignard reaction, introducing a magnesium bromide group (OMgBr).- **Step V:** The final step involves converting the Grignard intermediate to an amine alcohol product.This activity will help solidify your understanding of reagent selection in organic synthesis pathways. To preview image click hereChoose the correct reagents for the following synthesis.1. Correct reagent(s) for Step I - [ Select ]2. Correct reagent(s) for Step II - [ Select ]Options:A. HOCH2CH2OH/ROHB. 1 Equivalent HOCH2CH2OH/HCl (cat.)C. 2 Equivalent HOCH2CH2OH/HCl (cat.)3. Correct reagent(s) for Step III - [ Select ]4. Correct reagent(s) for Step IV - [ Select ]5. Correct reagent(s) for Step V - [ Select ]Diagram:- **Step I**: Starts with a cyclic compound with an alcohol and a ketone group.- **Step II**: Transformation involves the formation of another cyclic compound with an additional ketone group.- **Step III**: Another structural change leading to a cyclic ketone with an ester or related group.- **Step IV**: Introduction of a Grignard reagent (OMgBr) structure.- **Step V**: Final step leading to the formation of a compound with an additional hydroxide and amine group.The sequence displays the progression of a multi-step chemical synthesis involving cyclic compounds and functional group transformations.

To preview image click here Choose the correct reagents for the following synthesis. 1. Correct reagent(s) for Step | [Select] [Select] A. PCC/CH2C12 2. Correct reagent(s) for Step II B. Na2Cr207/H2SO4/H2O A or B 3. Correct reagent(s) for Step III [Select] 4. Correct reagent(s) for Step IV [Select] 5. Correct reagents(s) for Step V [Select] -OH || OMgBr IV H OH OH

To preview image click here Choose the correct reagents for the following synthesis. 1. Correct reagent(s) for Step | [Select] [Select] A. PCC/CH2C12 2. Correct reagent(s) for Step II B. Na2Cr207/H2SO4/H2O A or B 3. Correct reagent(s) for Step III [Select] 4. Correct reagent(s) for Step IV [Select] 5. Correct reagents(s) for Step V [Select] -OH || OMgBr IV H OH OH

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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