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OH con nomcom 1. NaOH, EtOH, A How would using 1-chlorobutane instead of 1-iodobutane affect the...
for the reaction: acetaminophen + (NaOH/EtOH note: etoh is ethanol) and butyl iodide ---------------> 4-butoxyacetanilide a) The first step in this reaction is to reflux acetaminophen in a NaOH/EtOH solution, followed by the addition of butyl iodide. What is the purpose of using the NaOH/EtOH solution? Would the SN2 reaction still occur if the first step was not completed? Why or why not? b) Upon completion of the reaction (before filtration), an additional 4.0 mL of 1.0 M NaOH/EtOH was...
Follow-up Questions 1. The Nal al/acetone test gives a precipitate with 1-chlorobutane and 1-bromobutane, but not l-iodobutane. Why? 2. Why is it important to use a polar solvent such as ethanol in the silver nitrate test? 3. A student decides to repeat the experiment using organochlorides (R-Cl) instead of organobromides. In the Nal test, would organochlorides react faster, slower or at the same rate as the corresponding organobromides? Explain. Would the order of reactivity change? Explain. b. In the AgNO,...
c) How does using triethylphosphite instead of triphenylphosphine affect the outcome of the Wittig reaction? Give an example. See text. 16.10B. 10" Ed. led assign the NMD enantu and the main honde includins the anchonul
Upon completion of the reaction (before filtration), an additional 4.0 mL of 1.0 M NaOH/EtOH was added to the reaction. What was the purpose of this step? Include a chemical reaction as part of your answer. [2 Marks] n this experiment you synthesize 4-butoxyacetanilide via a Williamson Ether Synthesis. OH 1. NaOH/EtOH 2. 4-butoxyacetanilide acetaminophen
OH EtOH, H* OH Br 1, NaOH 2. HCI compound compound b poud c SOCh compound 0 OMe HN LIAIH compound d compound f Cyclomethycaine The above reaction scheme presents one possible synthesis of eyclomethycaine. Work out the synthesis on a separate sheet of paper, and then draw the structure of compound f.
What would be the major product of the following reaction? CHO NaOH 100°C о OH you on or otor What would be the major product of the following reaction sequence? X 1. LDA, -18°C, 1. LDA, -78°C ? 2. PhCHBr OPh OH hmote are no Yome years Ph b. Phí d. e 7 Ph 9. What would be the product of the following conversion? 1. NaOEt, EtOH اOE = ? ہے 2. H30+ OH 0 O . لي OEt .هم..
4. If you use 0.20 M KI instead of 0.10 M KI, how would this affect (a) the slopes of your curves, (b) the rate of the reactions, and (c) the numerical value of k for the reaction?
1) In the lab of synthesis of aspirin, how will adding HCl instead of phosphoric acid affect the outcome of the experiment. 2) In the lab of synthesis of aspirin, what is the purpose of using KMnO4 solution? 3) Suggest 2 other ways(besides use of hickman still) that you can use to influence the direction of reaction equilibrium in the lab dehydration of alcohol to alkenes 4) How will the absence of hickman still affect the outcome of the experiment...
I would really appreciate it if someone can please help me with these question. Thank you, God Bless! Substrate Relative Reaction Rate with AgNO3 Relative Reaction Rate with NaI 1-chlorobutane 4 3 2-chlorobutane 3 2 2-chloro-2-methylpropane 1 4 benzyl chloride 2 1 1-bromobutane 4 3 2-bromobutane 3 4 2-bromo-2-methylpropane 1 2 benzyl bromide 2 1 1-iodobutane 2 2-iodobutane 1 mm fdgfd Q1. for the AgNO3 reaction, do you see any pattern between relative reaction rate and substrate structure? Q2. For...
Repeat Part I, using 1M NaOH instead of 1M HCI. Namely, perform five serial dilutions, recording the new concentrations and new pH after each dilution. [H] (OH) рн Data Table Solution Part 1 1M HCI (undiluted) Flask 1 Flask 2 Flask 3 Flask 4 Flask 5 -0.00 0.50 060. 0 90 025 0.625 0.03125 1.0X1o-14 2.0x10-10 40x10-14 8.ox 1014 16x10-13 3.2 x 10-13 1.0rlooly Part II 1M NaOH (undiluted) Flask 1 Flask 2 Flask 3 Flask 4 Flask 5 4.0x...