*Must complete all parts for positive rating.* Determine if the product(s) from each reaction is(are) correct and check the appropriate box. If incorrect, either check “No reaction” (if no reaction occurs) or provide correct product. DO NOT CORRECT REACTANT or REAGENTS.
*Must complete all parts for positive rating.* Determine if the product(s) from each reaction is(are) correct...
Please answer all parts for a good rating! Predict the product(s) for each of the following reactions. Pay attention to stereochemistry. In each case, a reaction occurs, even if it is simply an acid-base reaction А) HO но H+ NaOEt Он C) pH 4~5 NH2 BL 2) Predict the organic product(s) at each step in the following reaction scheme. Also provide the complete arrow-pushing mechanism for the full process. You may use -Ph as an abbreviation for a benzene ring...
Please answer all parts for good rating! 1) Predict the product(s) for each of the following reactions. Pay attention to stereochemistry. In each case, a reaction occurs, even if it is simply an acid-base reaction. NaOH H0 EtOH (solvent) SOCI, NaOEt D) HO CH H2SO4 (catalyst) NH H2O (solvent) " H2SO4 (catalytic)
PLEASE ANSWER ALL QUESTIONS 41) Provide the major organic product of the following reaction. Bry, FeBry 42) Provide the major organic product that results when benzene is treated with the following sequence of reagents: 1. HNO3, H2SO4 2. Br2, FeBr3. Answer: NO2 43) Explain why Friedel-Crafts alkylation reactions are prone to poly alkylation, whereas Friedel- Crafts acylation reactions are not prone to polyacylation? 44) Which series of reagents would be required to perform the following synthesis? A) 1. CICH2CH2CH3, AICI;...
In each reaction Predict the major organic product(s). Where necessary show appropriate stereochemistry and regiochemistry. DO NOT DRAW THE MECHANISM! 1) Br/FeBr 2) Separate p-isomer 3) CH3CH2B(OR)2/PdL2/NaOH 4) KMnO4/NaOH/A 5) H 0 1) Br2/FeBr3 2) Separate p-isomer 5) H30 3) CH3CH2B(OR)2 4) KMnO4/NaOH/A PdL2/NaOH C. C.
Please answer all parts for good rating! The following reaction will not result in complete conversion to the amide compound. Suggest all of the products (the main organic products as well as any by-products) and indicate the number of moles of each product formed and the approximate number of moles of each reagent remaining. The reaction takes place in an inert (non-reactive) solvent. NH u. CI 1.0 mol 1.0 mol Suggest the reagents and steps needed to synthesize the following...
Determine if the products from each reaction is correct and if not, provide the correct answer. If incorrect, No reaction or Correct Product NaSCH3 SCH; correct incorrect NaSCHs, schs No reaction or OEH If incorrect, Correct Product Br correct incorrect No reaction or t-BUOK If incorrect. Correct Product M ~ F correct foun, incorrect M If incorrect. r correct n No reaction or Nah, incorrect Correct Product
Please explain in details 3. Each reaction below is missing the substrate, reagent(s), or product(s), as indicated by the box. Write the missing substance(s) in the space provided to the right. Do not show any mechanisms or intermediates!!! Be sure to show stereochemistry where appropriate. If the products are missing, you must show all possible major products. If the s are missing, you must determine the number and order of reagents used. If the substrate is missing you only need...
In each reaction box, place the best reagent or reactant from the list below. Reagents may be used more than once or not at all. Draw the intermediate products B and C (both are neutral; omit byproducts). The six reaction boxes of the labeling scheme are correct. Examine the drawing area(s) marked as incorrect.
Please answer ALL questions and write clearly/neatly with explanations. I will give a positive rating. CEM 352 QUIZ 3: DUE Friday APRIL 3rd before 5:00 PM EST by EMAIL to your TA NAME: ID TA The following quiz contains 4 questions (see next page) and is worth 25 points. You may use your book, lecture notes and internet (but remember - not everything on the internet is true) to find the answers to the questions. There is also a 3...
(b) Provide appropriate starting material or reagents to complete each reaction below. You must show clear stereochemistry at all stereogenic carbons. ?? SCH3 N3 N3- Br