Propose a one-step synthesis of chloroacetone from acetone. Why can this reaction not be run under basic conditions? If the synthesis were attempted under basic conditions, what would the product be? Propose a mechanism for that process.
Propose a one-step synthesis of chloroacetone from acetone. Why can this reaction not be run under...
12. (6 marks) Propose are reaction mechanism for the 2-step synthesis of C from A & B. What is a key driving force for this reaction? CO Me CO2Me
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B and C. Note: each step consists of more than one transformation. Step 1 in slope fin Step 2 Hint: you can use Br 1. H', ethylene glycol, heat 2. NaOH/H, O, heat 3. H30* Product A Step 3 HCl dilute Product C Product B 1. PhMgBr, ether 2. H20 acetone Step 1: Step 2: Step 3: 3. Show the full mechanism of Step 3...
Propose a synthesis for the following conversion. It will take more than one step. Show the product of each reaction you propose to use. [6 points] CN
2. Provide missing conditions, reactants in the following synthesis. Propose the structures for Products A, B and C. Note: each step consists of more than one transformation. Step 1 Step 2 Hint: can use you 1. H, ethylene glycol, heat 2. NaOHH2o, heat 3. Н,о" Br Product A Step 3 HCI dilute PhMgBr, ether Product C Product B acetone 2. H,о" Step 1: Step 2: Step 3:
. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) Retrosynthesis HO O 04
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) но
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) i =
3. Propose a synthesis of the molecule below starting from acetone and using any reagent you like that contributes fewer than 4 carbons to the final product (5 points) HO
Propose a feasible mechanism for reaction which is occuring under BASIC conditions. Please include all steps and mechanistic intermediates. Use arrows and clearly indicate which atom holds charge. Draw only ONE resonance structure for any charge intermediates! QUESTION 11 Propose a feasible MECHANISM for the reaction shown below, which is occurring under basic conditions. NEATLY & CLEARLY draw all mechanistic intermediates; use arrows correctly to indicate bond making and bond breaking and clearly indicate which atoms(s), if any bear a...
This question is worth 10 points. Propose a synthesis to produce (2R,3S)-2,3-dibromobutane from acetylene. You can use any inorganic reagents you'd like. You don't have to draw the mechanism - only provide the reagents needed for each step of your proposed synthesis. Br ??? HH Br exclusive product