EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
9th Edition
ISBN: 9780136781776
Author: Wade
Publisher: PEARSON CO
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Chapter 15, Problem 15.26SP

Show how the reaction of an allylic halide with a Grignard reagent might be used to synthesize the following hydrocarbons.

  1. a. 5-methylhex-1-ene
  2. b. 2,5,5-trimethylhept-2-ene
  3. c. 1-cyclopentylpent-2-ene
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Students have asked these similar questions
1) Which of the following the alkyl halides reacts the fastest in an SN2 reaction? *   A. 1-Chloropropane B. 1-Bromopropane C. 1-Fluoropropane D. 1-Iodopropane E. Alkyl halides do not undergo SN2 reactions   2) The IUPAC name of the expected Markovnikov addition product of HI to 2-methyl-2-butene is __________.
Name the following compound according to the IUPAC method. CH3 CH2=CH-C- CH–CH3 Br OH A. 3-bromo-3-methyl-2-hydroxypent- 4-ene B. 5-formyl-1,3-dibromobenzene C. 3-bromo-3-methylpent-4-en-2-ol D. 3-bromo-3-methylpent-2-en-4-ol
A hydrocarbon, C6H12, on ozonolysis gives only one product which does not give silver mirror with Tollens' reagent. The hydrocarbon is ______________.   a. 3-Hexene b. 2-Hexene c. 2-Methyl-2-pentene d. 2,3-Dimethyl-2-butene

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EP ORGANIC CHEMISTRY -MOD.MASTERING 18W

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How to Design a Total Synthesis; Author: Chemistry Unleashed;https://www.youtube.com/watch?v=9jRfAJJO7mM;License: Standard YouTube License, CC-BY