I0 I. Suggest a synthetic route. Clearly show all intermediates (i.e intermediate products) and reaction conditions....
Propose a reasonable synthetic route for each of the following multistep syntheses. Show all isolable intermediates. D. E.
4. Propose a reasonable synthetic route for the following interconversions. Show all isolated intermediates. A lcohol Oxobtn PCC Cal kone olehydrohalogam alcoholic COt DEHTHE O'N OH joatinafalahal PCC OxgAautyon PCc oS onlcohol mgbr odottion Reaigont 135 OH OH 136
1. Provide the missing conditions for both steps and show how the amide can be converted to the corresponding acid chloride. Step 1 Step 2 Step 1 Conditions for step 1 (brain-twister: is there just one way?): Conditions for step 2 (same brain-twister): Full reaction scheme: 2. Consider the following reaction: 1. NaOM/MeOH 2. H,0* Does it have a specific name? How many products are possible? Show all of them. Suggest a synthetic route that leads to a lesser number...
suggest a simole synthesis for each of the compounds. Clearly show all required reagents and reaction conditions. NOTE: This is just a review of the reactions of alkenes Name: IV, Suggest a simple synthesis for each of the compounds. Clearly show all required reagents and reaction condition. NOTE: This is just a review of the reactions of alIKees CH3 CH3 Br нс. Cн, OH CH3 Он CH3 (END)
Suggest a simple synthesis for each of the compounds. Clearly show all required reagents and reaction condition. IV. Suggest a simple synthesis for each of the compounds. Clearly show all required reagents and reaction condition. NOTE: This is just a review of the reactions of alkenes (END)
Alkenes, Alkynes, Reactions 1. Give a reasonable mechanism for the following reaction. Clearly show all intermediates and show the movement of electron pairs with curved arrows. CHE CHE CH3 H20, (H2SO4) H20,(1900), HHQ CH.CH H3C он H₃C сна H₃C CH₂
Draw a detailed, stepwise mechanism to show how the products of this Sy1 reaction form. Clearly draw the structures of all reactive intermediates. Use curved arrows and include all formal charges. (0.7 pts)
2. Draw a detailed, stepwise mechanism to show how the products of this reaction form. Clearly draw the structures of all reactive intermediates. Use curved arrows and include all formal charges. Hint: both Sy1 and SN2 chemistry is required. (2 pts) Oor 21Oo..mo
1. Give stepwise mechanisms for the following reactions. Clearly show all intermediates and use arrows to show electron movement. - Hop Wow Peonic plure H-Br RO-OR, heat I Br b. R oh solla Red + S02 + Hl- c. Al cu. -CH = CH –O-CH3 Hbg, 4pH OH + HCl. 0 KOEI 1. Nat o Et, Etoh il I 10, EL + C CH₂ OH 2. Hoot TOE 1.HCl, H₂O 2. Et3N, Eto ce U
Supply structural formulas for all products for the reactants given below. Show all intermediates wherever it is known. 3)- Supply structural formulas for all products for the reactants given below. Show all intermediates wherever it is known. Choose 12 Problems Inclusive of H, K, L, 0; R. D/Pd/BaSO4 Quinoline, CH3OH IA] IB] D-NaNH2/Heat 2)-H20 ICI 1)-NaNH2/Heat 2)-H20 KOH(aq)/Heat IDI IE 2). I 12000C Na/NH3 IFI IGI HI THF 1)-Sia-BH 2)- H202 /OH H2O/H2SO IJ] HBr IL] IMI HI INI BrMg...