Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 11, Problem 11.49SP

Predict the major products (including stereochemistry) when cis-3-methylcyclohexanol reacts with the following reagents.

  1. a. PBr3
  2. b. SOCl2
  3. c. Lucas reagent
  4. d. concentrated HBr
  5. e. TsCl/pyridine, then NaBr
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From the table of reagents shown below, show how you synthesize the product from the given reactant. OCH₂CH3 OH a. NBS, (PhCO₂)2 b. Br2, FeBr3 c. Br₂, H+ d. OH e. NaOH(s), A f. HNO3, H₂SO4 g. H₂ CrO4 Reagents available h. CH3 CI, AICI, o. CuCN i. CH3 CH₂ Br p. H₂O+, A j. CH₂O, A q. CH3 CH₂ COCI, AICI, k. CH3COCI, AICI3 r. H₂NNH₂, OH, A 1. Mg, Et₂ O s. H₂, Pd/C m. CO₂ (s) then H3O+ t. H₂PO₂ n. HONO 0°C u. Cl₂, FeCl3 (Enter the letter(s) of the reagent(s) needed in the box, in the order that they must be used. No more than two steps are required to perform the synthesis. Note that a retrosynthetic arrow is used, and therefore the reactant is shown on the right.) Answer:
12. Which reagents/conditions would lead to the transformation depicted below in high yield? a. NaOMe, MeOH b. MeOH, H₂O* c. NaOEt, EtOH 13. In the structure of 2-fluoropropanoic acid shown, the oxidation number on C1 is the oxidation number on C2 is a. +1, +2, -3 b. -3, +1, +3 d. NaOH, H₂O e. two of these , and the oxidation number on C3 is, c. 0, 0, 0 d. +3,0,-3 e. +2,0, -2 ??? OH 14. What will be the outcome of the following reaction sequence? B. 1. NaOEt, EtOH 2. PCC 3. isopropylMgBr 4. H₂0¹ ??? a. 2-ethyl-3-isopropyl-2,3-dimethyloxirane b. 2,3,4-trimethyl-3,4-epoxyhexane c. 1,2,3,4-tetramethyl-2,3-epoxypentane d. Both a and b are suitable. e. All of the above are correct. OH 15. What is a suitable IUPAC name for the structure shown at the right? OH D. F H OH LOH CH3 3 OH
Provide the principle organic product for the following reactions. If more than one product is formed indicate which one you expect to be the major product.

Chapter 11 Solutions

Organic Chemistry (9th Edition)

Ch. 11.6 - Predict the products of the following reactions....Ch. 11.7A - Propose a mechanism for the reaction of a....Ch. 11.7B - Prob. 11.13PCh. 11.7B - Show how you would use a simple chemical test to...Ch. 11.7C - Neopentyl alcohol, (CH3)3CCH2OH, reacts with...Ch. 11.7C - Prob. 11.16PCh. 11.7C - When cis-2-methylcyclohexanol reacts with the...Ch. 11.8 - Prob. 11.18PCh. 11.9 - Prob. 11.19PCh. 11.9 - Prob. 11.20PCh. 11.9 - Prob. 11.21PCh. 11.10A - Prob. 11.22PCh. 11.10A - Some alcohols undergo rearrangement or other...Ch. 11.10B - Prob. 11.24PCh. 11.10B - Explain why the acid-catalyzed condensation is a...Ch. 11.10B - Prob. 11.26PCh. 11.10B - When the following substituted cycloheptanol...Ch. 11.11A - Prob. 11.28PCh. 11.11A - Prob. 11.29PCh. 11.11B - Predict the products formed by periodic acid...Ch. 11.12 - Prob. 11.31PCh. 11.13A - Prob. 11.32PCh. 11.14 - Prob. 11.33PCh. 11.14 - a. Show how ethanol and cyclohexanol may be used...Ch. 11.14 - Prob. 11.35PCh. 11.14 - Phenols (pKa 10) are more acidic than other...Ch. 11.14 - To practice working through the early parts of a...Ch. 11.14 - Prob. 11.38PCh. 11 - Predict the major products of the following...Ch. 11 - Show how you would convert 2-methylcyclopentanol...Ch. 11 - In each case, show how you would synthesize the...Ch. 11 - Prob. 11.42SPCh. 11 - Prob. 11.43SPCh. 11 - Prob. 11.44SPCh. 11 - Both cis- and trans-2-methylcyclohexanol undergo...Ch. 11 - Prob. 11.46SPCh. 11 - Prob. 11.47SPCh. 11 - Show how you would make each compound, beginning...Ch. 11 - Predict the major products (including...Ch. 11 - Show how you would use simple chemical tests to...Ch. 11 - The compound shown below has three different types...Ch. 11 - Prob. 11.52SPCh. 11 - Prob. 11.53SPCh. 11 - Prob. 11.54SPCh. 11 - Prob. 11.55SPCh. 11 - Show how you would synthesize the following...Ch. 11 - Show how you would synthesize the following...Ch. 11 - The following pseudo-syntheses (guaranteed not to...Ch. 11 - Two unknowns, X and Y, both having the molecular...Ch. 11 - The Williamson ether synthesis involves the...Ch. 11 - Prob. 11.61SPCh. 11 - Prob. 11.62SPCh. 11 - Alcohols combine with ketones and aldehydes to...Ch. 11 - Prob. 11.64SPCh. 11 - Prob. 11.65SPCh. 11 - Prob. 11.66SP
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