Study Guide/solutions Manual For Organic Chemistry
6th Edition
ISBN: 9781260475678
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Students have asked these similar questions
Consider the following SN 2 reaction:
مار
+
Br
H₂O
acetone
+ Br
OH
What effect would each of the following changes have on the rate of this reaction. Select the single best answer for each part.
Part 1 of 3
If the substrate was changed to:
The rate would
Br
O increase
O decrease
O remain unchanged
Part 2 of 3
×
S
If the nucleophile was changed to OH, the rate would:
O increase
O decrease
O remain unchanged
Part 3 of 3
If the solvent was changed to ethanol, the rate would:
Increase
O decrease
O remain unchanged
2
ol
Ar
Consider the following nucleophilic substitution reaction. The compound listed above the arrow is the solvent for the reaction. If nothing is listed over the arrow,
then the nucleophile is also the solvent for the reaction.
Part: 0/2
Part 1 of 2
Br
acetone
+ I
What is the correct mechanism for the reaction? Select the single best answer.
OSN 1
OSN 2
X
Part: 1/2
Part 2 of 2
Draw the products for the reaction. Include both the major organic product and the inorganic product. If more than one stereoisomer is possible, draw
only one stereoisomer. Include stereochemistry where relevant.
Click and drag to start drawing a
structure.
Х
5
☐
Triethyloxonium tetrafluoroborate reacts with ethanol (CH3CH2OH) to give diethyl ether (CH3CH2OCH2CH3).
BF
triethyloxonium tetrafluoroborate
Which equation, including the curved arrows, best represents the rate-determining step in the mechanism? Select the single best answer.
O
OH
CH3CH2
OH
+
H.
0+
CH₂H₂
:0
+
0+
ж
+
H
+
:0:
0
C
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