EBK ORGANIC CHEMISTRY
9th Edition
ISBN: 8220100591310
Author: McMurry
Publisher: CENGAGE L
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Chapter 8.5, Problem 9P
Interpretation Introduction
a)
Interpretation:
The structure of the product obtained by the hydroboration-oxidation of 2-methyl-2-pentene is to be given.
Concept introduction:
The hydroboration reaction takes place with syn stereochemistry and results in a non-Markovnikov addition of water to the double bond in an
To give:
The structure of the product obtained by the hydroboration-oxidation of 2-methyl-2-pentene.
Interpretation Introduction
b)
Interpretation:
The structure of the product obtained by the hydroboration-oxidation of the compound is to be given.
Concept introduction:
The hydroboration reaction takes place with syn stereochemistry and results in a non-Markovnikov addition of water to the double bond in the alkene. The resulting product has the hydroxyl group on the less highly substituted carbon.
To give:
The structure of the product obtained by the hydroboration-oxidation of the compound shown.
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Place the following characteristics into the box for the correct ion. Note that some of the characteristics will not be placed in either bin. Use your periodic table
for assistance.
Link to Periodic Table
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This anion could form a neutral
compound by forming an ionic bond
with one Ca²+.
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This ion forms ionic bonds with
nonmetals.
This ion has a 1- charge.
This is a polyatomic ion.
The neutral atom from which this ion
is formed is a metal.
The atom from which this ion is
formed gains an electron to become
an ion.
The atom from which this ion is
formed loses an electron to become
an ion.
This ion has a total of 18 electrons.
This ion has a total of 36 electrons.
This ion has covalent bonds and a net
2- charge.
This ion has a 1+ charge.
Potassium ion
Bromide ion
Sulfate ion
U
Consider the following graph containing line plots for the moles of Product 1 versus time (minutes) and the moles of Product 2 versus time in minutes.
Choose all of the key terms/phrases that describe the plots on this graph.
Check all that apply.
▸ View Available Hint(s)
Slope is zero.
More of Product 1 is obtained in 12 minutes.
Slope has units of moles per minute.
plot of minutes versus moles
positive relationship between moles and minutes
negative relationship between moles and minutes
Slope has units of minutes per moles.
More of Product 2 is obtained in 12 minutes.
can be described using equation y = mx + b
plot of moles versus minutes
y-intercept is at (12,10).
y-intercept is at the origin.
Product Amount
(moles)
Product 1
B (12,10)
Product 2
E
1
Time
(minutes)
A (12,5)
Solve for x, where M is molar and s is seconds.
x = (9.0 × 10³ M−². s¯¹) (0.26 M)³
Enter the answer. Include units. Use the exponent key above the answer box to indicate any exponent on your units.
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ΜΑ
0
?
Units
Value
Chapter 8 Solutions
EBK ORGANIC CHEMISTRY
Ch. 8.1 - Prob. 1PCh. 8.1 - How many alkene products, including E,Z isomers,...Ch. 8.2 - Prob. 3PCh. 8.2 - Addition of HCl to 1, 2-dimethylcyclohexene yields...Ch. 8.3 - Prob. 5PCh. 8.3 - Prob. 6PCh. 8.4 - Prob. 7PCh. 8.4 - From what alkenes might the following alcohols...Ch. 8.5 - Prob. 9PCh. 8.5 - What alkenes might be used to prepare the...
Ch. 8.5 - Tho following cycloalkene gives a mixture of two...Ch. 8.6 - Prob. 12PCh. 8.7 - Prob. 13PCh. 8.7 - Starting with an alkene, how would you prepare...Ch. 8.8 - Prob. 15PCh. 8.8 - Prob. 16PCh. 8.9 - What products would you expect from the following...Ch. 8.10 - Prob. 18PCh. 8.10 - Prob. 19PCh. 8.13 - Prob. 20PCh. 8.13 - What products are formed from hydration of...Ch. 8.SE - Name the following alkenes, and predict the...Ch. 8.SE - Prob. 23VCCh. 8.SE - Prob. 24VCCh. 8.SE - Prob. 25VCCh. 8.SE - Prob. 26MPCh. 8.SE - Prob. 27MPCh. 8.SE - Draw the structures of the organoboranes formed...Ch. 8.SE - Prob. 29MPCh. 8.SE - Provide the mechanism and products for the...Ch. 8.SE - Propose a curved-arrow mechanism to show how ozone...Ch. 8.SE - Prob. 32MPCh. 8.SE - Prob. 33MPCh. 8.SE - Prob. 34MPCh. 8.SE - 10-Bromo- α -chamigrene, a compound isolated from...Ch. 8.SE - Isolated from marine algae, prelaureatin is...Ch. 8.SE - Dichlorocarbene can be generated by heating sodium...Ch. 8.SE - Reaction of cyclohexene with mercury(II) acetate...Ch. 8.SE - Use your general knowledge of alkene chemistry to...Ch. 8.SE - Prob. 40MPCh. 8.SE - Hydroboration of 2-methyl-2-pentene at 25°C,...Ch. 8.SE - Prob. 42APCh. 8.SE - Suggest structures for alkenes that give the...Ch. 8.SE - Prob. 44APCh. 8.SE - Prob. 45APCh. 8.SE - Prob. 46APCh. 8.SE - Prob. 47APCh. 8.SE - Predict the products of the following reactions....Ch. 8.SE - Prob. 49APCh. 8.SE - How would you carry out the following...Ch. 8.SE - Draw the structure of an alkene that yields only...Ch. 8.SE - Show the structures of alkenes that give the...Ch. 8.SE - Prob. 53APCh. 8.SE - Which of the following alcohols could not be made...Ch. 8.SE - Prob. 55APCh. 8.SE - Prob. 56APCh. 8.SE - Prob. 57APCh. 8.SE - Compound A has the formula C10HI6. On catalytic...Ch. 8.SE - Prob. 59APCh. 8.SE - Prob. 60APCh. 8.SE - Prob. 61APCh. 8.SE - Draw the structure of a hydrocarbon that absorbs 2...Ch. 8.SE - Prob. 63APCh. 8.SE - The sex attractant of the common housefly is a...Ch. 8.SE - Prob. 65APCh. 8.SE - Prob. 66APCh. 8.SE - α-Terpinene, C10H16, is a pleasant-smelling...Ch. 8.SE - Prob. 68APCh. 8.SE - Prob. 69APCh. 8.SE - Prob. 70APCh. 8.SE - Prob. 71APCh. 8.SE - Prob. 72AP
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