Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN: 9780618974122
Author: Andrei Straumanis
Publisher: Cengage Learning
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Identify the sequence of reactions that successfully completes the following transformation.
Ph
A. 1. BH3 2. H₂O₂ / NaOH _3. P, l₂
B. HI, ROOR, hv
C. 1. HBr, ROOR, hv 2. Nal, acetone
D. Choices A and C
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- C. Show the product formed each step of this multi-step synthesis. Br2, H3O+ KOtBu NaOH, H₂O, A 1. Pr₂CuLi 2. H3O+arrow_forwardWhat is the major product of this reaction sequence? CIck on a letterA through D to answer. 1. EIONA/E1OH 2. BrCH-CH-CHз (1 еq.) 3. H30*, heat A. C. HO В. D.arrow_forward3. Draw all products for the following reactions. For your products, write whether the nucleophile added to the Re face or Si face of the starting material. a. HO b. 1) LIAIH 2) H™ 1) CH3CH2Li 2) H+ c) Determine whether the nucleophile added to the Re face or Si face of benzaldehyde.arrow_forward
- Identify the reagents needed to come up with the given compounds. Pls Separate the reagents with a comma and a space. (ex. HNO3, H2SO4). For a multi-step reaction, separate the reagents with a semi-colon. (ex. HNO3, H2SO4; CH3Cl, AlCl3) There should be 9 reagentsarrow_forwardMatch each reaction to a product. Answers may be repeated. Assume any necessary workup. Chiral products are racemic. D stands for deuterium, an isotope of hydrogen. OH a. b. OH d. e. not a.-d. NABD, Choose. BD3 NaOOH Choose.arrow_forwardDraw the product of the following reaction. Omit stereochemistry from the product structure. Check O 1. NaBH 4 2. H₂O Click and drag to start drawing a structure. Save For Later Sul 2024 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacyarrow_forward
- Which of the reactions below should be used to carry out the following alpha alkylation? He A. B. 1. LDA 2. Et-l 1. NaOMe 2. Et-l ? C. Both work equally well D. Not physically possible with A or Barrow_forwardWhat is the product of this reaction sequence? B. ОН A OB OC OD НО 2. LiAIH4 3. H2O, H, heat ОН _OH H+ D. ОН ? ОНarrow_forward1. Williamson Ether Synthesis Questions for lab , Synthesize phenacetin from acetaminophen (Tylenol) via a Williamson ether synthesis. a.Find the missing reagent:CH3CH2OH +? → C2H5OC2H5 H2SO4, H2O HNO3, H2CO3 b.What is the nucleophile in this reaction? H2O Nu- RO- ROH c.If you wanted to prepare Guaifenesin (present in OTC cough meds), choose the alcohol you would start with? 2 methoxy benzoinc acid 2-methoxy benzaldehyde 2-methoxyphenol 2 methoxy anisole d.What was the mechanism of the reaction you used to prepare the ether? SN1 SN2 E1 E2 e.The reaction given below is known as by which o the following reaction? C2H5ONa+IC2H5→C2H5OC2H5+NaI Oxidation reaction Williamson reduction reaction Williamson ether synthesis Wittig synthesis f.Chloroethane reacts with X to form diethyl ether. What is X?…arrow_forward
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