2/ Through Retrosynthetic analysis, explain how you would proceed to obtain this product starting from bromocyclohexane:
1/ Through Retrosynthetic analysis, explain how you would proceed to obtain this product starting from bromocyclohexane: og
וווו והו vide a retrosynthetic analysis to show how you would synthesize the following molecule. As starting erials you may use any alcohols of 5 carbons or less. You may use any necessary solvents and inorganic eagents. There is no need to show reaction mechanisms, just reactants, conditions and products (10 points). HyC
Please help with all parts!! Thank you!!
6. Practicing retrosynthetic analysis and devising reasonable routes to final targets: a. Starting from iodobenzene, provide a forward synthesis for halide/pseudohalide Provide a forward synthesis for each of the four products below, starting from bromocyclohexane. c. Provide an efficient forward synthesis of the ether from 2-chlorobutane. d. Starting from the 1,1-disubstituted alkene, provide a forward synthesis for the tetrasubstituted alkene. a. b. OTs он он CI or d. C.
6. Practicing retrosynthetic analysis...
9.RETROSYNTHETIC ANALYSIS Give a reasonable synthesis for the following compound from the indicated starting materials. You may use any other organic reagents or inorganic reagents you wish. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate), and products of each synthetic step but NO MECHANISMS. [4 points) OH Use to make HO
one possible answer is a wittig rxn. please explain how?
4) Consider the following retrosynthetic analysis: this way more than 1 Product Br This is one potential way to form the target alkene on the left: elimination from the corresponding alkyl halide. What's another unique pathway (can't involve an elimination) that would allow you to form this alkene? Describe this alternative. Would there be an advantage to this alternative pathway? What would that be? (20 Pts)
2. Perform a retrosynthetic analysis on the following molecule from the given starting materials (13 pts). Me Me O Me Me Me Et Me OEPr 1 11 2 3. 10. Me Me Me 7 ΕΙ Me Br
2. Retrosynthetic Analysis-place the starting material(s) in the box provided. он 0 From an Aldol Addition Reaction From an Intramolecular Aldol Reaction Ic) From a Mixed Aldol Condensation Reaction
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2. Perform a retrosynthetic analysis on the following molecule from the given starting materials (13 pts). Me e Me Me Me O.PT 1 11. 2 3. 10 Me Me Me Me Br
(d) Perform a retrosynthetic analysis of molecule A. Using propiophenone as starting material outline the forward synthesis also. Explain how a similar route could be taken to afford a mixture of diastercoisomers B and C OH OH propiophenone
please explain why the answer is the answer step by step
Retrosynthetic Analysis Give a reasonable synthesis for each of the following compounds from the indicated starting materials. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. If equal mixtures are anticipated (ie. ortho/para products) then indicate...