Activity 4: Chem 334 MW, 1114/19 (it is recommended you show as much work as possible...
show mechanism and arrows 11.) Provide the mechanism for each step and the final product for the following series of reactions. (5 points) "Y 2.) A8:0, 10, 1.) excess CH31 2.) Ag20, H2O, A 13.) Provide the mechanism for each step and the final product for the following series of reactions. (25 points) 1.) HNO3/H2SO4 2.) Zn (Hg), HCI 3.) HNO/HCI 4.) H30+, A 5.) O o
please help! im stuck on these questions ! 11.) Provide the mechanism for each step and the final product for the following series of reactions. (5 points) Н 1.) excess CH31 2.) Ag2O,H,O, A 13.) Provide the mechanism for each step and the final product for the following series of reactions. (25 points) 1.) HNO3/H2SO4 2.) Zn (Hg), HCI 3.) HNO/HCI 4.) H30*, A 5.) 0
Acavity : Chem 334 RM11141 It is recommended you show much work as possible for partial credit) 10.) Show the mechanism for the following reaction and determine what the main product is (5 points) HẠN NH 2) NOH, MO 13.) Show the mechanism for the following reaction and show both possible products. (5 points) N Ag 0,10
13.) Provide the mechanism for each step and the final product for the following series of reactions. (25 points) 1.) HNO3/H2SO4 2.) Zn (Hg), HCI 3.) HNO2/HCI 4) H,0, A 5.) o
Name: CHEM 330 Homework #9 Due: 11/06/19 1. Provide the major product for each of the following reactions. If a racemic mixture is produced, you must show them both. (Remember to consider regio- and stereoselectivity) (18 pts) HCI 1) Hg(OAC)2, ETOH 2) NaBH 1) BH; 2) H2O2, NaOH H30* 1) BH3 2) H2O2, NaOH HBr H₂O₂ H2, Pd
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion. CCH3 Choose the correct reagents for step 1. CH3CH2Cl / AICI Cl2 / AICI Bry/ FeBry CH3CCI / AICI: Choose the correct reagents for step 2. NON CH3CH2C / AICI Cl2 / AICI Bry/FeBry o CH,CCI/ AICI Predict the major product for the following reaction. CI/AICI: ОН ОН ОН 0 none of these Provide the reagents necessary to carry out the following conversion. Choose...
Part I: Organic Synthesis. Show as much work as possible to receive partial credit If required (30 points) 15. What is the product of these reactions? (10 points) 1) CHỊCH,MgBr 2) H0 3) H2SO4 (aq) heat 4) Hg(OAc), H,O-THF 5) NaBH, 16. Propose a sequence of chemical steps in the proper order to synthesize the desired product. (10 points) OH oleh OH 17. Propose a sequence of chemical steps in the proper order to synthesize the desired product. (10 points)...
Do all work on this paper. 1. The compound below on the left has a much higher melting point than its isomer on the right. Explain. (4 points) Tronohon o llottobu 2. Strong acids always protonate amide oxygens and never protonate amide nitrogens. Provide two reasons that explain this fact (4 points). 3. Draw the complete mechanism of the reaction below and indicate the location of "O in the product. (6 points). CH, + 1 equivalent of KOH in water...
CHEM 2343A HOMEWORK W13 Name: DUE 11/18/19 at 9:10 AM There are total of 4 questions on this homework assignment 1. For the reaction outlined below in la and I draw out the reaction mechanism using arrow formalism to describe how the reaction below occurs. Be sure to draw out all action intermediates & the moment of all electrons needed to justify the formation of the indicand product. You do not need to add in any reagents that are not...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 pts) (30 points total) 30 Unsat. Index = (2C+2-H-X+NY2 = 200 25 e = 2.00 ppm, 4.90 f = 1.27 ppm, 20 720 Compound 18a: C,H,O, singlet, 2H triplet, 3H 127 15 d = 2.66 ppm, a = 7.21 ppm, b = 7.18 ppm, doublet, 2H doublet, 2H C = 4.90...