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 9.10A, Problem 9.23P

Predict the product(s) you would expect from treatment of each compound with (1) dilute, neutral KMnO4 and (2) warm basic KMnO4, then dilute acid.

  1. a. hex-1-yne
  2. b. hex-2-yne
  3. c. hex-3-yne
  4. d. 2-methylhex-3-yne
  5. e. cyclodecyne
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Choose the best reagents from the list provided below for carrying out the following conversion.  Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acid
Organometallic reagents and alkoxides are strong bases as well as being good nucleophiles. Given the pKa values below, which reagent is the stronger base, nBuLi (CH3CH2CH2CH2LI) or the tert-butoxide anion ((CH3)3CO‒)? Explain your choice clearly in terms of structure andbonding. (Comparing the pKa values is not an explanation.)  (CH3)3COH pka= 16.54CH3CH2CH2CH3 pka= 50
I need help on the order of the listed reagents to make the final product.

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Organic Chemistry (9th Edition)

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