please show work! 1. 1. Provide the full name for the following molecule. (0.5 pt) 1....
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1) Name the following compounds: (8 pts) Br 1a) 1b) 2) Draw the major product and write a mechanism for the reaction. (12 pts) Br NaOET EtOH, 60 °C 3) Draw the major product and write a mechanism for the reaction. (10 pts) HBr, 0°C Draw the major product of the reaction shown below. Propose a detailed mechanism for the reaction. HBr...
Problem #3 Provide the full IUPAC name for the following molecule. Problem #4 Draw the substitution product from each of the following reactions. HgSO4 1 BH-THF 2. H2O,, NaOH O CH H.SO, 1,6 Extra Credit Show how you would accomplish the following conversion. More than one step is likely necessary.
1) Provide the starting material for the following reaction. (0.5 pts) Он Он 1) Hg(OAc)2, H20 2) NaBH (provide starting material) 2) Provide the major organic product(s) for the following reactions. If stereoisomers are formed, please show both stereoisomers. (0.5 pts each) 1) BH3 THF a) 2)120 NaOH 1) NaOH, H-O, 55°C b) 2) OsO4 t-BuOOH 1-BuOH, NaOH Br2 c) CCl4 H2O, H2SO d) H9SO4 2 equivalents HBr e) 3) The following ction generates an ether. Provide the major organic...
Name: CHEM 330 Homework #9 Due: 11/06/19 1. Provide the major product for each of the following reactions. If a racemic mixture is produced, you must show them both. (Remember to consider regio- and stereoselectivity) (18 pts) HCI 1) Hg(OAC)2, ETOH 2) NaBH 1) BH; 2) H2O2, NaOH H30* 1) BH3 2) H2O2, NaOH HBr H₂O₂ H2, Pd
Question 21 6 pts Please show your work for full credit. Platinum-170 has a half-life of 14.0 ms. How long in milliseconds) would it take for a sample of 170Pt to become 75.0 % decayed? D Question 22 9 pts Please show your work for full credit. For the following reaction: + HBr = ? A. (4 pts) Name the organic reactant. B. (5 pts) Provide the structure of the product (Note: You must clearly draw this on your paper...
1. (a) Draw the products for the following Sy2 reactions (0.5 pt ea) (b) Designate all asymmetric carbons as R or S (0.5 pt ea) CH3 OSOH + Bracetone P:EN: + , scelone, :OCH + Door NCCHE 2. (a) Draw the products for the following Syl reactions. (0.5 pt ea) (b) Designate all asymmetric carbons as R or Sor racemic. (0.5 pt ea) CH,OH - - - #20+ ytor - 3. (a) For the reactions below, predict the mechanism (Snl...
2. (a) Draw the products for the following Snl reactions. (0.5 pt ea) (b) Designate all asymmetric carbons as R or Sor racemic. (0.5 pt ea) cH:OH + I Br Br H:O: + 40: 1 28 -
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2. Provide the major product for the following reactions. 1. 12, NaOH, H2o 2. HCI (workup) 1. LDA 2. CH3CH2CH2Br 1. t-BuONa cyclopentanone 1. EtoNa 2. 1-Bromopentane 3. NaOH 4. Hyo*, heat 1. EtONa 2. Benzyl chloride 3. NaOH 4. H 0*, heat
2. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, product intermediate structure and name (please show which carbon carriers charges if possible)," chemistry is involved, please indicate "anti" or "syn" at the end of the reaction equation. Please name the product. Please indicate "follow Markovnikov's rule or not follow Markovnikov's rule". (If hydride shift is possible, please consider it and show it in your reaction) 1-1) Reaction of the following with HBr in electrophilic addition reactions H3PO4 2) pent-1-ene...
Question 1 Predict the major product(s) for each of the following reactions. Show both enantiomers if a racemic mixture is formed: 1) MCPBA 2) H3O 1) BH3 THF 2) H202 NaOH HBr Br, H2 Pt