Two synthetic schemes (Sceme 1 and 2) have been proposed for the target compound, the details are discussed as below.
The starting material used below is diethyl malonate instead of dimethyl malonate, which may not be so critical to achieve the target compound as required. I apologize for the same.
suggest 2 different synthesis methods Using the starting material on the left, synthesize the product on...
5. Using the starting material and any compound with 1 or fewer carbons, synthesize the product shown below. (2.0) Zb starting material on a manner AOH starting material OR
6) Multistep synthesis from cyclohexane Using cyclohexane as your starting material, show how you would synthesize cach of the following compounds. Once you have shown how to synthesize a compound, you may use it as the starting material in any later parts of this problem.) a) bromocyclohexane (b) cyclohexene e) ethoxycyclohexane (d) 3-bromocyclohex-l-ene (e) cyclohexa-1,3-diene (1) cyclohexanol
Provide a multistep synthesis for the desired product using the indicated starting material. You may use any additional reagents you wish, but all carbons in the starting material must end up in the product. Do not draw any curved-arrow mechanisms. The best answer will require seven or fewer steps. Starting Material ou (+/-) Desired Product
Provide a multistep synthesis for the desired product using the indicated starting material. You may use any additional reagents you wish, but all carbons the starting material must end up in the product Do not draw any curved-arrow mechanisms. The best answer will require nine or fewer steps. H Starting Material (+/-) Desired Product
Propose multi-step chemical syntheses for the product on the right from the starting material provided, they require more than one step. You can use any reagent with up to four carbons. Show the product for each step in your synthesis. 5. 110 points] Chose TWO of the following transformations and propose multi-step chemical syntheses for the product on the right from the starting material provided. All syntheses require more than one step. You can use any reagent with up to...
5 (20 pts) (a) Propose a reasonable synthesis, using indicated diketone as starting material. ri and any C4 or less starting materials (SMS) (any reagents are allowed) Hint: as a C3 SM use (6) Propose two syntheses, which will use two distinct methods for construction of the 6-membered ring (1) Crossed-Claisen condensation and (2) Claisen condensation(s). 0 0 selor must use this reagent plus any acyclic Cg or less
Suggest a reasonable synthesis for the following compound using the given starting material and anything else you need. Question 3 (9 points) Suggest a reasonable synthesis for the following compound using the given starting material and anything else you need. (Hint: Show the intermediates, not only the conditions, for partial credit) ОН several steps
8. Synthesis: Using the starting materials below as your only carbon sources, synthesize the desired product (hint: you will have to use the ester multiple times!)
02. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) (you can also use any one C reagent)
Q2. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) Do (you can also use any one C reagent) ОН (you can also use any two carbon reagent)