Inorganic Chemistry
5th Edition
ISBN: 9780321811059
Author: Gary L. Miessler, Paul J. Fischer, Donald A. Tarr
Publisher: Prentice Hall
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Chapter 8, Problem 8.42P
On the basis of VSEPR, predict the structures of
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Draw the structure of (E,6R) 6-methoxy-4-hepten-2-one.
Give the IUPAC name of this compound,
including stereochemistry.
Draw the most stable chair conformation of
(cis) 1,3-isobutylcyclohexane.
H
HC=CCH₂
CH2CH3
EN(CH3)2
-CN(CH3)2
10. Write out the mechanism (intermediate/transition state) for this reaction; indicate
stereochemistry in product.
H3C
CH₂OH
CH3
SN1
H
Write "most" under the member of each trio which is most stable.
Write "least under the member of each trio which is least stable.
b)
Draw a Fischer projection of a pair of enantiomers with three chiral carbons.
Which of these two would you expect to be more soluble in
water? Why?
1-butanol
1-heptanol
Which of these two would you expect to have the higher boiling
point? Why?
hexyl methyl ether
1-heptanol
Chapter 8 Solutions
Inorganic Chemistry
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