provide the mechanism for the following reaction 4. Show the detailed mechanism for the following reduction...
4. Show the detailed mechanism for the following reduction of propanenitrile to propanal using DIBAH in toluene. 1) DIBAH, Toluene, -78°c NHA Hас Hас 2) H+, H2O
show the detailed mechanism for the following reaction. Hac 1) DIBAH, Toluene, -78°C 2) H+, H,0 LHC40 + NH, N
Provide a detailed reaction mechanism for the NaBH4 reduction ( no text, just draw the mechanism ) Provide the general equation of the acetalization reaction
Draw the organic product(s) for the following chemical reaction. Underneath each reaction, provide a detailed mechanism(using arrows) of how the product is produced when required. FeCl3 n o + ch Fello Cl2 No Mechanism Polymerization Initiator *Since this is a polymerization, show the polymer using appropriate brackets. No Mechanism. H2O* Mechanism: "The above molecule polymerizes with itself. Show the polymer that is formed Mechanism: (show the formation of the trimer) 2) Draw the organic reactant(s) for the following chemical reaction....
Show the complete detailed mechanism for the following reaction. Provide all possible products and indicate specific stereochemistry or regio-chemistry if appropriate Cl B. NaOH. H,O → 2 350°C products
5. Mechanism: (20 pts) Show the detailed reaction mechanism including all relevant arrows, intermediates, inorganic products, relevant resonance structures, and stereochemistry for the following reaction heat OH H-Br Step 1 step 2 Step 3 Step 4 Product(s) a. This is a Sx2/S1/E/Ez/ reduction / oxidation mechanism. b. What is the product if the starting alcohol is reacted with PBry? Product(s) with PBry c. Reaction with PBr; is a S2/S1/E/Ez/reduction / oxidation mechanism.
5. Mechanism: (20 pts) Show the detailed reaction mechanism including all relevant arrows, intermediates, inorganic products, relevant resonance structures, and stereochemistry for the following reaction. heat OH H-Br step 1 step 2 step 3 step 4 Product(s) a. This is a S2/Sx1/E/E2/ reduction / oxidation mechanism. b. What is the product if the starting alcohol is reacted with PBrz? Product(s) with PBrz c. Reaction with PBr3 is a S2/S1/Ej / E2 / reduction / oxidation mechanism.
Please show detailed arrow-pushing mechanism. Best regards. C) Please provide the product of the following reaction and concisely explain why you get the observed constitutional isomer. Drawing the appropriate orbitals will really help to explain your answer. (2 points box, 4 points explanation, 6 points total section). 1 H O-Na H Mel
4.(18 points) Using the arrow, provide the detailed reaction conditions necessary to give the following. You do not need to provide any starting material or product, just the reaction conditions (see example below) 1.B Example: Show reagent 'B' followed by aqueous acid: 2. H30 a. Markovnikov addition of H2O to a double bond: b. Anti-Markovnikov addition of H2O to a double bond: c. Markovnikov addition to form an alkyl bromide from an alkene: d. Reaction conditions to change 1,2-dimethylcyclohexene into...
4. Bonus mechanism problem:. Provide a detailed, step by step mechanism for the following reaction. Explain the unexpected regiochemistry. 1) HNO3 H2SO4 2) NaOH NO2