need help in mechanism...this is clemmenson reduction
need help in mechanism...this is clemmenson reduction Cag Pho cis Can
Need some help!! 1. Predict the product and provide a detailed, stepwise mechanism for the reduction of the compounds shown below. Use curved arrows to show the movement of electrons. (You can assume LIAIH4 was added in excess) 1. LIAIH4 2. H20 1. LIAIH4 N-H 2. H20 1. LIAIH4 2. H20
Describe the mechanism for the reduction of an alkyne using a dissolving metal reduction. A) What is unique about this mechanism which we have not seen in any previous mechanism covered in this course? B) Why is it that this mechanism is stereoselective? C) What causes it to form only the trans alkene and not the cis?
sodium borohydide reduction of 4 tert butylcyclohexanone. need help confirming top answers are correct and help with lower section. thanks & Draw your two products (each in the most stable chair conformation) below using the numbering provided. Show only the -OH and tert-butyl groups on the ring. a) label each group as equatorial (eq) or axial (ax). b) label each group as top face (top) or bottom face (bot). OH (ax, top) (ax, bot) .OH (Eq, top 7 (Er, top...
I need help on the mechanism of this reaction with the arrows Mechanism Explorer: Sketch and Submission Reaction Explorer Help (Intermediate) Reactant (Intermediate) Product Apply Mechanism но- H2C Hint Solution CH3 H3 H3 н,с он 3 remaining step(s) can be solved 2 possible next steps unlocked. Click on [Hint) or [Reset] to cycle through them. H2C Tip: Only add curved arrows in this sketcher
Draw the reaction and reaction mechanism for the reaction of both cis and trans stilbene with Br2 as part of your prelab procedure. Note: I'm not sure what the mechanisms look like so that's why I'm having trouble with the products. Please, if you can, draw out the mechanisms for both of these!! Thanks. cis-stilbene trans-stilbene
I need help with this mechanism. If somone could explain what happened here, because I'm at a loss. Or if someone can give me the name of the mechanism. Thank you! OH
need help on polymer chemistry question Determine which polymerization mechanism(s), i.e. radical, anionic, and cationic, can be used for the following monomers. Briefly explain your answer. H2C=CHCI HỌC =CHCN H2C= C(CN)
need help on polymer chemistry question Determine which polymerization mechanism(s), i.e. radical, anionic, and cationic, can be used for the following monomers. Briefly explain your answer. H2C=CHCI HỌC =CHCN H2C= C(CN)
need help on polymer chemistry question Determine which polymerization mechanism(s), i.e. radical, anionic, and cationic, can be used for the following monomers. Briefly explain your answer. H2C= CHCEH H2C= C(CH3)2 H3CHC=CHCH
Please help with this mechanism Draw the mechanism for the reaction of an alkyl halide with sodium azide, followed by reduction. Follow the directions on each step. Complete the mechanism of the initial step of the reaction of the alkyl halide with sodium Complete the product structure by adding any missing atoms, bonds, charges, and nonbonding electrons. Omit curved arrows. Predict the organic product of the LAH reduction and hydrolysis steps; include nonbonding electrons. Do not include any inorganic products.