without using Huckel's Rule. Lopts) © Diaw the detailed Mechanism for the following reaction (10 pts)...
Part 4 (3 pts) Draw a stepwise, detailed mechanism for the following reaction. Beste OCH
provide the mechanism
43. Provide a complete, detailed mechanism for the reaction shown below. (10 pts). What is the type of mechanism?
provide the mechanism
44. Provide a complete, detailed mechanism for the reaction shown below. (10 pts). What is the type of mechanism? • MgBr 2) H30
4.Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the following reaction: (20 pts.) H₂ CH₂ CH,OH CH H.C. H₂C Н.С. OCH, CH, 880.
(10 pts) able, detailed, stepwise mechanism for the reaction of 1. Mechanism - Carbonyl to Imine: Provide a reasonable, detailed, stepwise mechanism fo p-toluidine with 3-pentanone. (Initially, be concerned about making the ketone a better ele Label important intermediate(s). As appropriate, show important resonance structures) We were unable to transcribe this image
(10 pts) 1 Mechanism - Carbonyl to imine Provide a reasonable detailed stepwise mechanism for the reaction of -toluidine with 3-pentanone initially be concerned about making the ketone a better electrophile.) Labelmportant intermediates) AS Oropriate show important resonance structures) (6 pts) 2. Nomenclature: Supply the IUPAC name for the following compound
provide the mechanism for the following reaction
4. Show the detailed mechanism for the following reduction of propanenitrile to propanal using DIBAH in toluene. H₃C EN 1) DIBAH, Toluene, -78°C 2) H+, H,0 H₂C 0 + NH₃
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....
(10 pts) 1 Mechanism - Carbonyl to imine Provide a reasonable detailed stepwise mechanism for the reaction of -toluidine with 3-pentanone initially be concerned about making the ketone a better electrophile.) Labelmportant intermediates) AS Oropriate show important resonance structures) (6 pts) 2. Nomenclature: Supply the IUPAC name for the following compound
5. Give the products of the following reactions. You DO NOT need to show a detailed mechanism but do show ALL reaction intermediates. (30 pts) LiAIH4 G CH3-C-00HE (b) F (c) OH CH3 6. Give the product of the following reactions and in each case give a detailed reaction mechanism by which it is formed. (40 pts, 10 each) pH 4-5 ca. H2S4 HBrJ (c)--/SH NaOH I (d) H CH3 H CH3
5. Give the products of the following reactions....