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This product can be formed by the Dields- Alder reaction. Dield- Alder reactions are carried out in polar organic solvents such as dimeththylformamide and ethylene glycol and even in water. Diene and dienophile react in presence of heat to form the product
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- R 400m N CO₂tBu OH CO₂Me Ph LDA THF, -78 °C silica gel 6 days room temperature R MeO₂C NCO₂Bu CHO CO,Me I + H₂Onurbuks alixir 9 and lead). solution of ammonium chloride ) (~Hyl) acetate (Pb(CH3006) ₂ This solid? produces a solid. What is the identity of Bott A. Pb (CH₂COO), B. Pb (NH4)₂ C. (NH4), 4 D) Pb C (W) J Ẹ NH, CH, Coo Expl 49 42-0 CO C-PF St LGO (23 21 HO SA R الموت id boke slit + CXIC moth SHMOB stata GStructure pK, K. Name NH; CHCH,-O 2.20 (СО,Н) 9.31 (NH,) 6.3 X 10-3 4.9 x 10-10 Phenylalanine CO,H 7.11 x 10-3 6.34 x 10-8 2.148 * 7.198 Phosphoric acid* (hydrogen phosphate) НО — Р— Он 12.375 4.22 X 10-13 OH (1.5) 6.78 3 x 10-2 1.66 x 10-7 HP- он Phosphorous acid (hydrogen phosphite) OH 1.12 x 10-3 3.90 x 10-6 2.950 Phthalic acid (benzene-1,2-dicarboxylic acid) 5.408 cO,H Piperazine (perhydro- 1,4-diazine) 5.333 9.731 4.65 x 10-6 1.86 X 10-10 11.125 7.50 x 10-12 Piperidine 1.12 x 10-2 2.29 x 10-11 -co,H 1.952 (СO,Н) 10.640 (NH,) Prolinc +H 4.874 1.34 x 10-5 Propanoic acid CH,CH,CO,H H,C=CHCO,H 4.258 5.52 x 10-5 Propenoic acid (аcrylic acid) 10.566 2.72 x 10-11 Propylamine CH;CH,CH,NII; 5.20 6.3,X 10-6 Pyridine (azine) Pyridine-2-carboxylic acid (picolinic acid) (1.01) (CO,H) 5.39 (NH) 9.8 x 10-2 4.1 x 10-6 co,H HO,C Pyridine-3-carboxylic acid (nicotinic acid) 2.03 (CO,H) 4.82 (NH) 9.3 x 10-3 1.51 x 10-s NH+ 1.4 (POH) (u = 0.1) 3.44 (OH) (1p. = 0.1) 6.01 (POH) (u = 0.1) 8.45 (NH) (u =…
- c. Indicate and provide structures of potential phase II metabolites. OMe OH F "CO₂EtOWLv2 Online tea x Search Results | Co x Paraphrasing Toal x enow.com/ilrn/takeAssignmenit/takeCovalentActivity.dolocatorassignment-take I Activity Log - USTA M Inbox - patrickcent. EMISTRY References] Use the References to access iimportant values if needed for tthis qu Consider the following half-reactioans: Half reaction E V) F2(g + 2e 2F (aq) 2.870V Cu"taq) + 2e Cu(s) 0.337V AF(ag) + 3e Al(s) -1.660 V (1) The weakest ozidizang agent is enter formula (2) The strongest reducing agent is (3) The strongest oxidizang agent is (4) The weakest reducing agent (5) Will F (aq) reduce AF (aq) to Al(s)? (6) Which species can be oxadized by Cu (ag)? If none, leave box blank Submit Answer Try Another Version 3 term attempts remaning Cengage Learming Cengage "echical Supportenow.com/ilrn/takeAssignment/takeCovalentActivity.do?locator-assignment-take ist: anxiet... E COVID-19 and Nig... ▪▪▪ Coronavirus: A vis... Preq Ereg req req req C $ 4 8 In the illustration: The product that forms is The limiting reagent is The number of C The number of product molecules formed is % 5 Corona virus: Cos... MP People who rely o... G covid 19 and the e... [Review Topics] [References] Use the References to access important values if needed for this question. G Search or type URL 1 The illustration to the left represents a mixture of hydrogen (light blue ) and iodine (purple) reacting to form a product. 6 Cengage Learning Cengage Technical Support atoms/molecules in excess is & 7 ☆ * 8 X ( 9 < 0 C Ho
- (k) (1) Me. an allene CH₂ CO₂Me Ph N₂ a. TsN 3, DBU b. Rh₂(OAC)4 CO₂Me Rh₂(OAC)4Apatent that weights 180-b will take 40 mgkg of ammonium chioride How many millters of an ammonium chioride (N4Clnw. 53 5) injection containing 5 mEgim should be added to the patient's rtravenous infusion? ... Answers A-D A 94mi B 24 4ml 122m 6.1mi A patient that weighs 180 pounds will take 40 mg/kg of ammonium chloride. How many milliliters of an ammonium chloride NH4CI-m.w. 53.5 injectio. containing 5 mEq/ml should be added to the patients intravenous infusion?O 11:E9 5310107675680311588_2 50.What is the pH of a 0.10 M solution of trimethylamine (pKs = 4.13)? 17 51.How would you calculate K, for the formate ion, given that the K, for formic acid is 1.8 x 10-4? (Kw=1.0x 10-14) K = K, x Kw b. K = Kw/K, c. K, = K/K d. K = Kw + Ka e. K = Kw - K, a. II
