MASTERING ORGANIC CHEMISTRY W/ETEXT >I
MASTERING ORGANIC CHEMISTRY W/ETEXT >I
14th Edition
ISBN: 9781269926454
Author: Pearson
Publisher: PEARSON C
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Chapter 4.12, Problem 32P

Draw all possible stereoisomers for each of the following:

  1. a. 2-chloro-3-hexanol
  2. b. 2-bromo-4-chlorohexane
  3. c. 2,3-dichloropentane
  4. d. 1,3-dibromopentane
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Which molecule will have a higher boiling point and why a.   molecule ‘b’ will have a higher boiling point as the molecule is more compact and therefore will pack better.   b. molecule ‘b’ will have the higher boiling point as the methyl groups are tetrahedrally arranged around the central carbon, giving it higher symmetry. c. molecule ‘a’ will have a higher boiling point as it has a greater surface for London dispersion forces. d. molecule ‘a’ will have a higher boiling point as it has a higher molecular weight than molecule ‘b’.
A.Oxidation cant be performed to tertiary alcohols. CHOICES: True False B. Alkynes have sp2 hybridized carbons CHOICES: True False C. A diene has the same no. of pi bonds as an alkyne. CHOICES: True False D. It is possible to reduce aldehydes to primary alcohols. CHOICES: True False
Draw a structure for each compound (includes old and new names). ) 1,3-cyclohexadiene

Chapter 4 Solutions

MASTERING ORGANIC CHEMISTRY W/ETEXT >I

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