Show the steps required to form the product. Include the reagants needed to complete each step and the intermediate products.
The steps are given in the image
Show the steps required to form the product. Include the reagants needed to complete each step...
Provide a total synthesis including all reagants needed to complete each step. You may start with any organic or organometallic molecule containing four carbons or less. он
show all of steps required to achieve the transformation shown below. For each step include all applicable starting material(s), solvent(s), reagents or catalysts required. You should show each step as a balanced reaction, but you do not need to draw full mechanisms. [3.0 Marks 0
31) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. CH он 32) Provide the reagents necessary to complete the following transformation. More than one step is needed. Show the structures of any intermediate products. Br он enantiomer HO tto prss 33) Provide the reagents necessary to convert 3-methyl-2-butanol into 2-methyl-2-butanol. More than step is needed. Show the structures of any intermediate products. Page 7 of 8
11. (8 points) Determine the product at each step in the following reaction and show the mechanism for the first three steps (but not Hz/Lindlar) | 1) xs NaNH, 1) NaNH, CHCI 2) H, 0 2 ) Lindlar Brz Br 12. (4 points) Devise a synthesis and show the mechanism (unless it is hydrogenation or hydroboration) for each product from the given starting material. More than one step is required for each. both products will form
Please show all steps and include how to determine the equivalents needed The final step in the synthesis of naproxen (the active ingredient in the commercial painkiller Aleve) involves a Williamson ether synthesis. Propose a mechanism for the transformation shown below. Include all charges and intermediates and stoichiometric equivalents of each of the reagents used (i.e. 1 equivalent, 2 equivalents, excess, etc...). [3 Marks] OH DY" – 6607 naproxen
Consider the following reaction: OH HC H.SO CH, + ОН Δ Show the complete mechanism for the following transformations. Make sure to show all arrows depicting the movement of electrons. The above reaction (using acid and heat) causes a number of unwanted side products to form (a big mess). Propose a better synthesis for the product using the same starting materials. Show the reagents and intermediate steps to complete the synthesis: OH H3C- ??? + CH3 OH X steps Propose...
Show each step required for the following synthesis. Show all intermediate compounds and reagents needed. new - OH
Identify major product and include stereochemistry if needed. Show all steps to get product with curved arrows to denote electron movement, please. 1. NaOH 2. H20+ 3. Heat
14-15) Predict the product. Show each step. 16-17) Predict the product. If no reaction, write NR. 14.) Predict the product. Show each step. of CH₂Br 2) con 7.) Mg 3.) H₂or 15.) Predict the product, Show each step 1.) Soch 2.) Li Al(O+-BuzH 16.) Predict the products. If no reaction, write NR. of ccl + CH₃OH Ht 1.) @ My Br Excess 2.) H₃O+ 7
Can someone show the steps to reach each product for both pictures. I am just confused about the inbetween steps as to where it attacks. Thanks! Predict the Product. Provide the stable organic product(s) for the reactions below. MgBr (1 eq.) 1. Mgº, CH,CH,OCH.CH 3. H2O, HCI 1. CH,MgBr (xs) 2. H,O, HCI 1. Mgº, CH3CH2OCH2CH3 2. DO Mechanism. The following Grignard reaction has been observed to yield products A and B. olo de Bolo 2. HCI, H,0 (. Org....