please provide the full reaction scheme including all steps LiAIHA OH OH Number of steps: 10...
Please show all the work, including steps and
mechanisms.
55) Provide the structure of the major organic product(s) in the reaction below Br Answer Diff: 2 Section: 9.7 LO: 9.4 GO: G2 MCAT LO: MCAT9.2
Provide the necessary reagents to complete the following
transformations. Please number your steps.
OH C3 C) HO OH
Please draw out the full mechanism with intermediates of this
reaction scheme. Thanks.
Reductive amination is usually a one-pot procedure during which a carbonyl compound is reacted with ammonia or a primary amine to yield an imine. Subsequently the imine is reduced in situ to an amine. The procedure has application in synthesis of biologically active molecules. In this experiment the imine will be prepared quantitatively through a solvent free reaction (green chemistry) between ortho-vanilin and para-toluidine. The imine is...
please provide the mechanism for the reaction to produce A and B as
well !
OH HO paraformaldehyde NH OAc NH2OAC Ph EtO OEt EtO но Н.о NT B A Scheme 3. Hantzsch Ester synthesis under aqueous conditions O:
please provide a full explanation on how you got the answers and
please answer all of the questions!
1) Name the following compounds: (8 pts) Br 1a) 1b) 2) Draw the major product and write a mechanism for the reaction. (12 pts) Br NaOET EtOH, 60 °C 3) Draw the major product and write a mechanism for the reaction. (10 pts) HBr, 0°C Draw the major product of the reaction shown below. Propose a detailed mechanism for the reaction. HBr...
Please give a FULL reaction mechanism (including any cleavage/proton and electron movement.... so please include all arrows) for benzaldehyde and the following reactions: - tollens test - schiff fucshin test - fehlings test
Complete the reaction scheme. Complete structures are required; if a reagent has a common abbreviation, then the abbreviation can be used but must be completely correct. Sequential steps should be numbered. Include stereochemistry as appropriate. 15. The Robinson Annulation combines two reactions to form a cyclica.B-unsaturated ketone. Provide the dicarbonyl intermediate and the final product. You do not need to worry about stereochemistry 15a. Draw the expected intermediate son OH (solvent) 10 15b. Predict the product. 10
Please provide all steps and a detailed explanation
12. Phosphorus pentachloride can be produced by the reaction of phosphorus trichloride and chlorine gas. What mass of phosphorus trichloride must be used to produce 127 g of phosphorus pentachloride if the percent yield is 84.8%?
Please provide the major organic product(s) of the reaction as
described. Account for all stereochemistry requirements for
reaction and products.
1) NaH, DMF, -78 C d) CI 2) NaOH e) Br OH 1
Please provide full clear steps
22) Calculate Vout(t) (10 pt) Remember to calculate impedance for each component. 0.5F 5cos(2)V 80 Vout