Can you please show all the steps and reagents used to form this product. Thank you so much:)))
Can you please show all the steps and reagents used to form this product. Thank you...
propose a synthetic route to carry out the following
transformation. do not show the mechanism. provide only the
reagents needed and the intermediate for each step of your
sequence. the most efficient solutions take two or three synthetic
steps.
6) Show how to carry out Select the appropriate reagents ar how to carry out the following transformation in the highest yield possible. Select the appropriate reagents and draw the correct organic product at each step.7) Propose a synthetic pathway for the following reaction. It might take more than one step to obtain the product.
all part of one question please answer neatly,
Part B Write the steps and reagents required to perform the following synthetic transformation. You may need more than one step. Page 17 CH2-B1 + H₂N Protein CPMV chanism for the hydrolysis of the ester below in basic solution Pag КОН CH
Problem IV. Synthesis (24 points). These transformations will require multiple steps. Provide the reagents for each step and draw out your proposed synthetic intermediates. Please do not draw curved arrows; this prob- lem is not asking for mechanisms. You do not need to provide solvents for the reactions. (1) (12 points) Provide a synthetic route-i.e., a sequence of reactions-to produce compound SS from compound RR using any other starting materials and reagents you wish. RR (2) (12 points) Provide a...
Provide the reagents and conditions for the following synthetic
transformation. Be sure to include all synthetic intermediates. You
will need more than one step to accomplish this.
Please show all of your steps.
Thank you!
5 (20 pts). (a) Propose a reasonable synthesis, using indicated diketone as starting material. ini ² and any C4 or less starting materials (SMS) (any reagents are allowed) Hint: as a C3 SM use Br (b) 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). must use this reagent plus any acyclic Cg or less BONUS (5 pts). In...
1. Provide reagents that could be used to convert the starting material to the final product shown. More than one step is required. You may list the reagents in order or show each step in the synthetic sequence. 2. Indicate a plausible mechanism for the following reaction. Be sure to show bond making and bond breaking as well as all electron movement. Every arrow counts. Be precise! Don't forget to show charges where necessary. If stereochemistry is involved, please show...
1. Provide reagents that could be used to convert the starting material to the final product shown. More than one step is required. You may list the reagents in order or show each step in the synthetic sequence. 2. Indicate a plausible mechanism for the following reaction. Be sure to show bond making and bond breaking well as all electron movement. Every arrow counts. Be precisel Don't forget to show charges where necessary. If stereochemistry is involved, please show it....
Organic ChemistryPlease show all reagents used,
the mechanism, and the product of each reactant.
27) Devise a multistep synthesis for the following transformation. You may use any organic or inorganic reagents of your choice. Include the reagents necessary for each step and the product of each step. -
Quickly show all steps and answers all parts of the question
please thank you
2. Show the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CH3 OH conc. HBO CH₂ H₂CX Br CH₂ H3C CHE H₃C CH Swi condition Br L CH3 CH3 H₃C HC X X