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

The following synthesis requires more than one step. Specify the reagents you would use to carry it out.

this is org chm hw

1) Using any reagents necessary (Cn, n<5 incorporated into final product), develop a synthesis for the following conversion. 8-8

Please help

Can you please tell me the reagents/conditions of each step 1, 2, 3 and possible occuring problems (for example: side reaction)? If there's any issues, please explain why the step works well.

Can you please tell me the reagents/conditions of each step 1, 2, 3 and possible occuring problems (for example: side reaction)? If there's any issues, please explain why the step works well.

6) Determine the reagents Needed, show each step. Br HOLL

Devise a 4-step synthesis of the product from the starting material. CH3 1. reagent 1 2. reagent 2 H3C HO. 3. reagent 3 4. reagent 4 H3C H. Select reagent 1: Select reagent 2: NH, CH,, cat. H,0+ CH, MGB. Select reagent 4: H, Pd NaBH, LIAIH,

Draw the organometallic reagent with all covalent bonds. There are two ways this target molecule could be made utilizing the more effective reaction you chose above. Draw the starting material and organometallic reagent necessary. For this part, draw the combination with the organometallic reagent with fewercarbon atoms. ÇH, H,C H,C