3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You...
b. Page 4 (Question 4 continued) Propose reasonable syntheses for the following indicated compounds and using any other necessary orga Show all intermediates formed to receive full credit ÇO2H I NO₂ for the following compounds beginning with the ng any other necessary organic or inorganic reagents. CHE SO3H OCH2CH3 [3% +6% marks] c. Outline the synthesis of the following compound using either the aceu meester synthesis method. Draw the structure of the starting material and show all intermediates, reagents and...
8. Alcohols are readily available synthetic starting materials. Propose a series of reactions to achieve the following syntheses starting from alcohols. Clearly show the reagents used for each step and the synthetic intermediates. a. For this synthesis, use the given starting alcohols and any inorganic reagents needed. You may use the two alcohols in separate reactions as needed. M OH + OH ... i
Page 4 Propose reasonable syntheses for the following compo compounds and using any other necessary organic intermediates formed to receive full credit. Assume separated. ng compounds beginning with the indicated organic or inorganic reagents. Show all sume any isomers formed can easily be [3% +6% marks] c. Provide any required reagents and give the stru following synthetic scheme. If more than one reaga steps. ve the structures of the intermediates in the one reagent is required, please number the Bra,...
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 (i.e. ortho / para products) then indicate where separations are needed. NO MECHANISMS! [6 points 2. Give a...
Propose syntheses of the given compounds from the indicated starting materials. он NH2 CH30
Propose syntheses of each of the following compounds, from the given starting material and any other needed reagents. » O- CH2OH from O con b) CH3CCHz from CH3CH=CH2 ОН • OCHGHs from O-Br
What are the following syntheses for each compound? 7. Propose a synthesis for each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. осон steps H₂C (ra (racemic) Hoc OH Hac CH3 сна N-OH steps
Propose a set of reagents (and steps) for syntehsizing the following molecules from their starting materials. You may use any reagants, solvents, and conditions you deem necessary. Place your answers above and below the reaction arrow. Please provide explanation and any concepts to study regarding the topic. Problem #3 Propose a set of reagents (and steps) for synthesizing the following molecules from their starting materials. You may use any reagents, solvents, and conditions you deem necessary. Place your answers above...
Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the intermediates formed. Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the intermediates formed. *Note: This will require more than 3 steps* ohin 3...
Show how each of the following compounds could be prepared using the given starting materials. Please Explain #Show how each of the following compounds could be prepared using the given starting materials, @ HCECH → M © HECH -Y © HC ECH - > D = sehr HCECH (35,4R)-4-bromo-3-hexanol and (30,45) -4- bromo-3-hexand