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 11.6, Problem 11.11P

Predict the products of the following reactions.

  1. a. cyclohexylmethanol + TsCl/pyridine
  2. b. product of (a) + LiAlH4
  3. c. 1—methylcyclohexanol + H2SO4, heat
  4. d. product of (c) + H2, Pt
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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. Predict the products of the following reactions. HBr a. OH conc. H₂SO4 heat b. C₁ H₂C d. H CH3 OH OH H H Br₂/ heat Br NaOCH₂CH3 ethanol heat -CH3 NaOCH₂CH3 ethanol heat A HO 9. OH h. X Br f. j. OH conc. H₂PO4 heat SOCI₂ G conc. acid heat NaOCH 3 methanol heat methanol
iii. Write the mechanism of the product formed. NaOH(aq) a. CH3CH2Cl b. CH3 H₂O CH3C CH2 Br CH3

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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