Acavity : Chem 334 RM11141 It is recommended you show much work as possible for partial...
Activity 4: Chem 334 MW, 1114/19 (it is recommended you show as much work as possible for partial credit) Name: 11.) Provide the mechanism for each step and the final product for the following series of reactions. (5 points) 1.) excess CH31 2.) Ag,0,H,O, A 13.) Provide the mechanism for each step and the final product for the following series of reactions. (25 points) 1.) HNO/H2SO4 2.) Zn (Hg), HCI 3.) HNO/HCI 4.) H30, A 5.) O o
Show the mechanism for the following reaction and show both possible products. 13.) Show the mechanism for the following reaction and show both possible products. (5 points) Ag20, H20
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)...
Help Please! Show all work Problem Set 12 October 16, 2019 CHEM 1252 Textbook Reading Assignment: 14.1-5 Additional Practice Problems: 14.1,7,13,17,19,23,25,29,31,41-42,47,53,55,58,61 1. What does it mean when we say that chemical equilibrium is a dynamic process? 2. Write an expression for Kor K, (whichever is more appropriate) for each of the following reactions, and give typical units (if any) for the equilibrium constant. (a)Na(e) + O2(g) - 2 NO(g) (b) 2012(g) + 2H2008) - 4HCI(g) + O2(g) (c) 1(aq) +...
Please be detailed as much as possible. THANK YOU VERY MUCH! Show the synthesis mechanism of the reaction sequence shown below . . + Na NM, 2-CH(CH, CHO ; 3. H* (quehchi n); 4. 4/Pa (fe, IParid ioe 55. ) / 40, hydrogenation of 3-hexyne 2. Show the intermediates and the products in the trans (CH₃ CH₂ C = CCH₂ CH₃) with Na/NH3 (liquid)? o. What products will form upon ozonolysis 10 lexcess) and reductive work up can lH20) of...
11. Show the product and use arrows to show the mechanism for the Nucleophilic Aromatic Substitution Reaction below. Assume benzyne is an intermediate. Just write B: to representa strong base reacting with the aromatic ring. (5 points) strong base NH 12. Show the kinetic and thermodynamic product formed in the reaction of 1,3-dibutene with Brzand draw an energy diagram for both products. Show both products on the same graph with energy on the Y axis and reaction coordinates on the...
Please show all work! Thank you so much 4. (0.5pt) When a single compound contains both a nucleophile and a leaving group, an intramolecular reaction may occur. With this in mind, draw the product of the following reaction. OHS но CH1002 Br Br Bro 5. (7pts) Draw a stepwise, detailed mechanism for the following reaction. N. ci CH3NH2 (excess) CH3NH3
HW 5 1. Draw all possible products for the base catalyzed reaction of ethanal and propanal. Indicate the new bond formed. (Full: all possible products and correct ID of new bond, partial: 75% of possible products) 2. Draw and label the kinetic and thermodynamic products for reacting the following ketone with LDA. (Full: correct products and labeling, partial: correct products but no labels) 1. LDA 2 CH31 3. Show the mechanism for the following intramolecular reaction. You do NOT need...
Show all work for the following problems answers only. partial credit will be given for work clearly shown. NO CREDIT will be given for .... . (10 points) If 1.000 g of chromium metal produces 1.461 g of chromium oxide, what is the empirical formula of the product?
CHEM 3020 Practice exam 3 Give the major organic product for the following reactions: R0, H.2 HO HO Bry 1) Lithium Disopropylamide (LDA) 2) CIES o spomen 1) Lithium Disopropyl anide (LDA) OCH, CITOTT 1) OHI 2) CHI OH Give all possible products from the following mixed aldol reaction and show how they can be formed. Show the mechanism for the keto enol tautomerization of 2-propanone in both acid and in base.