62. Show how the following compound can be synthesized from the given starting material. (Hint: Start with an acetoacetic ester.) OH sodinto antes O bio boogie COOH 63. Show how the following compounds can be prepared from cyclohexanone: CCH2CH2CH3 wolle CH CH.CH CH CCH boob TISU shots 0551 ollor O CH2 OH
Provide the arrow pushing mechanism from Cyclohexanone to Compound A, AND Compound A to Compound B. MgBr PhS Li 1 1 2. ΚΗ, ΤΗF Δ THF, -78°C 2. HBF4 A В
Synthesize the following compound from cyclohexanone and organic halides having ≤ 4 C's. You may use any other inorganic reagents. Draw all reaction intermediates, and select the single best set of reagents for each of the four reaction steps. Cyclohexanone
How could each of the following compounds be prepared from cyclohexanone? Problem 17.16 Part A Drag the appropriate labels to their respective targets. Reset Help 1. LDA THF 1. LDA/THF 1. LDA THF Part B Drag the appropriate labels to their respective targets. Reset Help 1. LDA THF Br 1. LDA THF 18 1. LDA THF Br Part Drag the appropriate labels to their respective targets. Reset Help 1. LDA/THF 1. LDA THF 1. LDA THF
Outline a synthetic method for the preparation of the compound shown below starting from cyclohexanone. Use any reagents that are needed. CH,Br Target Molecule
The following compound results from base-catalyzed aldol cyclization of a 2-substituted cyclohexanone. Starting with the diketone, propose a mechanism for the cyclization. o
QUESTION 12 Prepare the compound shown below from cyclohexanone (use as many molecules as needed) and organic compounds of three carbons or less as the starting materials. Show the product of each synthetic step and indicate all necessary reagents and reaction conditions. Count carbons carefully! os
Starting from cyclohexanone, how would you create the following molecule?
Show how the following compound could be prepared from ethyne. Please show all stable intermediates formed along the way & all necessary reagents used so i can better understand. multiple steps! Am HI
mechanism and 9) Provide the sequence of synthetic steps necessary to convert cyclohexanone into the compound shown CO2Et ise mechanism for the transformation shown below