What reagents could be used to carry out the following syntheses?Complete the syntheses by dragging the labels to the appropriate targets.1. H₂, Lindlar catalyst2.RCOOH01. R₂BH/THF2. HO, H2O2, H₂ORCH2CH3H₂O/H2SO4, HgSO4RCH=CH2RCH-CH2RCHCH3excess HBrBrRC CHBrexcess H₂, Pd/CRCCH3H2/Lindlar catalystBr1 equiv HBrRC=CH21.H2/Lindlar catalyst2. HBrBrRCCH30RCH2CHResetHelp

Step 1: Information: Markovnikovs Rule : In an addition reaction the negative part of reagent goes…

Answered: What reagents could be used to carry…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Draw the major product(s) from the reaction sequence below. Show all intermediate products. 1. KMnO4, NaOH, A 2. LAH, THF CH3 1. NBS, hv 2. +-BUOK Naᵒ, EtOH NH3(1)
In the following series of reactions, write the product (s) or the reagents needed to obtain the indicated product.
In which case is it correctly given which reagents should be above the arrows in the reaction given below?
Please complete the following synthesis. 0+x(4- Br A Br₂, hv F NBS K heat B Br₂, DCM G H₂, Pd 3 с HBr, DCM H LDA L Grubb's Br 2 Culi D HBr, H₂O I KMnO4 M CH₂l₂, Zn E HBr, H₂O₂ J 1. Li, 2. Cul
Do the reactions below proceed in good yield from left to right as shown? 8 a) b) H₂N-CH3 CH3OH excess u • ok. OCH3 + trace of Na OCH 3 Na O НО. OCH3 byl obl.. + Na OCH3
21. For the reaction described below. CH3 Select the best reagents: a) 1. OsO4, pyridine 2. NaHSO3, H₂O b) 1. Hg(OAc)2, H₂O 2. NaBH4 c) 1. RCO3H, CH2Cl2 2. H3O+ d) 1. BH3, THF 2. H₂O2, OH CH3 "OH 20 hetos to dess the c
3. Identify the products (A-G) of each reaction sequence shown below OH 1) HCI 2) KCN E Br NaOCH 3, CH3OH 1) PCC 2) CH3MgCl 3) H3O+ 4) CrO3, H₂SO4, H₂O 1) LDA, THF, -78 °C 2) CH31 A (C7H12O) C (C4H8O) F (C5H₂N) 1) Br₂, H* (cat.) 2) Li₂CO3, LiBr, DMF 1) LDA, THF, -78 °C 2) CH3CH₂CI 1) LDA, THF, -78 °C 2) CH3CH₂Br ¹H NMR: 6 6.7 (t, 1H); 2.4 (t, 2H); 2.3 (q, 2H);| 2.1 (s, 3H); 1.9 (quint., 2H) 13C NMR: 8 198; 144; 142; 36; 33; 27; 23. D B ¹H NMR: 8 2.5 (q, 2H); 2.4 (t, 2H); 1.6 (sextet, 2H); 1.1 (t, 3H); 0.90 (t, 3H) 13C NMR: 8 210; 45; 36; 18; 14; 8. G (C7H13N)
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10. Provide the product and mechanism for the following reactions. HBr NaOH H20 1. NaNH2 `H 2. Br 1. Br2 2. H20 Br NaCN acetone
Which of the following synthetic routes is the one that will most successfully generate a. 1. Brz. CH,COOH CH,CH,CH,C-OEt CH,CH,CH=CHC-OEt 2. Pyridine, heat b. ÇH, CH,CH,C-COOH 1. Na* OEt CH,(CO,Et), 2. CH,CH,Br 3. Na* OEt 4. CH,Br 5. H,O*, heat с. 1. Na* OEt CH,CH,C-OEt H,C=CHCH,CH,COOH 2. Н.С-СHCH, Br 3. Н, о", heat d. ÇO̟Et ÇO̟,Et ÇH, -CHCOOH 1. Na**OEt CH,CH-CO,Et 2. PhBr 3. H,O*, heat
Complete the following tree of reactions by providing their major products: HCI i. BH3 ii. NaOH, H₂O2, H₂O 03, (CH3)2S H+, H₂O Br₂ H₂, Pd/C CH₂CO3H Br₂, H₂O modellen H+, CH3OH
Fill in the boxes with reagents or products and show the mechanism.

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