Please dont reject, i got this wrong on practice and cannot figure it out To preview image click hereChoose the correct reagents for the following synthesis.1. Correct reagent(s) for Step 1 [Select]2. Correct reagent(s) for Step II [Select]3. Correct reagent(s) for Step III[Select][Select]4. Correct reagent(s) for Step IV B. CH3CH2MgBr/THFHA. 1. CH3CH2OH/MgBr 2. H3O+5. Correct reagents(s) for Step V [Select]-OHHC. 1. CH3CH20MgBr/THF 2. H3O+OMgBrIVHOHVOH

To preview image click here Choose the correct reagents for the following synthesis. 1. Correct reagent(s) for Step I [Select] 2. Correct reagent(s) for Step II 3. Correct reagent(s) for Step III [Select ] 4. Correct reagent(s) for Step IV B. CH3CH2MgBr/THF -OH [Select] [Select] A. 1. CH3CH2OH/MgBr 2. H3O+ = 5. Correct reagents(s) for Step V [Select] C. 1.CH3CH2OMgBr/THF 2. H3O+ OMgBr IV H OH 1 V OH

To preview image click here Choose the correct reagents for the following synthesis. 1. Correct reagent(s) for Step I [Select] 2. Correct reagent(s) for Step II 3. Correct reagent(s) for Step III [Select ] 4. Correct reagent(s) for Step IV B. CH3CH2MgBr/THF -OH [Select] [Select] A. 1. CH3CH2OH/MgBr 2. H3O+ = 5. Correct reagents(s) for Step V [Select] C. 1.CH3CH2OMgBr/THF 2. H3O+ OMgBr IV H OH 1 V OH

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 50CTQ

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To preview image click here Choose the correct reagents for the following synthesis. 1. Correct reagent(s) for Step | [Select ] 2. Correct reagent(s) for Step II 3. Correct reagent(s) for Step III 4. Correct reagent(s) for Step IV 5. Correct reagents(s) for Step V H -OH ||| [Select] [Select] [Select] [Select] [Select] A. NH2CH(CH3)2/HCI (cat.) B. NH2C(CH3)3/HCI (cat.) C. NHCHCH3/HCI (cat.) H OMgBr H Y OH OH
To preview image click here Choose the correct reagents for the following synthesis. 1. Correct reagent(s) for Step I [Select] [Select] A. PCC/CH2C12 2. Correct reagent(s) for Step II B. Na2Cr207/H2SO4/H20 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] H -OH 11 ||| OMgBr H H OH OH
Use the image below to answer the following three questions. Note: Subscripts are not shown in answer choices, ex: H2 should be H2, NH3 should be NH3. Product A Product B Product C a. The reagents that would selectively yield ProductA are [ Select] b. The reagents that would selectively yield Product B are [Select] c. The reagents that would selectively yield Product Care [Select]
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A H2N. Figure 9: Multi-step reaction sequence
Use the image below to answer the following three questions. Note: Subscripts are not shown in answer choices, ex: H2 should be H2, NH3 should be NH3. Product A Product B Product C a. The reagents that would selectively yield Product A are [Select] b. The reagents that would selectively yield Product B are [ Sclect] c. The reagents that would selectively yield Product C are [ Select]
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Choose the correct order of reagents to complete the following synthesis. To preview image click here Br OH Step 1 [Select] [Select] Step 1 Na2Cr207/H2SO4 Step 2 PCC/CH2C12 1. LIAIH4 2. H3O+ Br Step 2 8 Br
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Use Figure 2 and Figure 3 to explain if you made a pure product or had unreacted reagents. First Picture - shows figure 2 and 3 Secons Picture shows my own results for the product to compare with.