?Provide a synthesis for the following reaction. Any other molecule may be used as an additional reactant.
?Provide a synthesis for the following reaction. Any other molecule may be used as an additional...
20. (8 pts) Provide a synthesis of the following molecule starting from cyclohexene and any other reagent necessary complete the synthesis. Any other necessary reagent + -OCH2C3 20. (8 pts) Provide a synthesis of the following molecule starting from cyclohexene and any other reagent necessary complete the synthesis. Any other necessary reagent + -OCH2C3
4. Design a synthesis for the following molecule. You may only use carbon containing reagents if they are in the list on the right. You may use any other non-carbon containing reagents that you would like. Target molecule: Carbon containing molecules that you may use (you don't have to use all of them): -Br Out NaCN Br CO2
Provide a step-wise synthesis of the molecule shown below using the two starting materials provided and anything else you may need. 5. Provide a stepwise synthesis of the molecule shown below using the two starting materials provided and anything else you may need. a. anything plus any other molecule containing 1 C plus any other reagents necessary. cl Hint: this is a highly convergent synthesis. You will need to prepare two separate molecules, then birng them together to form the...
Organic Chem 2: please help! 26) Provide a detailed, stepwise synthesis for preparing the molecule on the left below from the molecule on the right and any other reagents necessary Br он
3) Propose a synthesis scheme for the following molecule from benzene using any reaction conditions. 4) Propose a synthesis scheme for the following molecule from benzene using any reaction conditions. NH2
Concept- Design a synthesis of 4-Cyanocyclohexene Design a synthesis of 4-cyanocyclohexene from 2-bromopropanenitrile and any other compounds using a Diels-Alder cycloaddition reaction. CN Br CN and any other compounds Part 1 out of 7 Choose the best option for the diene precursor to the target molecule CN diene dienophile CN CN
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
Provide a stepwise synthesis for the following reaction. you may use the indicated starting materials as well as any organic or inorganic reagents.
2. Propose an efficient synthesis (less than 5 steps) of the following molecule from benzene. You may use any additional material and show all intermediates. Br HO
Provide a reasonable multistep synthesis of the following molecule from the indicated starting material, using any reagents necessary. (Please include the product and reagents of each individual step in your synthesis. DER