Synthesis: Using your knowledge of organic reactions, show a synthesis for the following preparation. You must show all steps with reagents for full credit. No curved arrows please! CI Br
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- Cs Scanned with CamScanner 2. Show two reaction schemes to synthesize the following compounds. Pick one reaction scheme and draw the step-by-step reaction mechanism. а. HO-show all steps and use the arrows correctly. Propose a mechanism that explains the product for the following reaction. Be sure to ILO H₂SO, OH XoDraw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS. SHOW ALL INTERMEDIATES. 1) NaOH 2) H3O* H3C H3C HO
- Propose an efficient multistep synthesis for the transformation shown below. There is no need to show the mechanism of any step, only the reagents required for each step, and the resulting intermediate product of each step. 1ouborq sto vino noib restriction: The given reactant is your only source of carbon atoms, but you may use more than one molecule of the reactant. multiple steps + en. OaTSynthesis: Synthesize the following compounds using the starting material shown a reagents you may need. Show the product after each step. You do not need to shc and I will assume standard work up unless you indicate otherwise. HO, ÕH5) Determine reaction conditions needed for a multiple step synthesis to transform the starting material into the product. Show the product after each step (but you do not need to show reactive intermediates or mechanisms). OH
- NH 1) xs Mel 2) Ag2O, H2O, A 2. Complete the following reaction. Show the intermediate, and propose a mechanism for the second step.In light of the fact that tertiary alkyl halides undergo spontaneous dissociation to yield a carbocation plus halide ion (see Problem 10-45), propose a mechanism for the following reaction.Multi-step synthesis: Provide reagents needed for the following transformations. More than ne step is rquired for each reaction.
- Predict the product and provide a suitable mechanism. The reaction proceeds through a rearrangement. What is the name of the rearrangement? Based on the rearrangement, write the product of the second reaction.Show the complete conversion for the two reactions below. If more than one step is required, show the major product for each reaction used. For instance, after each reactant you must show the resulting structure. No need to show the mechanism.Propose an efficient syntheses of the product from the starting material.Show all reagents you need over each arrow, and draw all products andintermediates (do not combine steps).
