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Pearson eText Organic Chemistry -- Instant Access (Pearson+)
8th Edition
ISBN: 9780135213711
Author: Paula Bruice
Publisher: PEARSON+
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Textbook Question
Chapter 19, Problem 33P
- a. Draw resonance contributors to show why pyridine-N-oxide is more reactive than pyridine toward electrophilic
aromatic substitution. - b. At what position does pyridine-N-oxide undergo electrophilic aromatic substitution?
Expert Solution & Answer
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The sum of the numbers in the name of isA. 11; B. 13; C. 10; D. 12; E. none of the other answers iscorrect. I believe the awnser should be E to this problem but the solution to this problem is D 12. I'm honestly unsure how that's the solution. If you can please explain the steps to this type of problem and how to approach a problem like this it would be greatly appreciated!
Consider the following data for phosphorus:
g
atomic mass
30.974
mol
electronegativity
2.19
kJ
electron affinity
72.
mol
kJ
ionization energy
1011.8
mol
kJ
heat of fusion
0.64
mol
You may find additional useful data in the ALEKS Data tab.
Does the following reaction absorb or release energy?
2+
+
(1) P (g) + e
→ P (g)
Is it possible to calculate the amount of
energy absorbed
or released by reaction (1) using only the data above?
If you answered yes to the previous question, enter the
amount of energy absorbed or released by reaction (1):
Does the following reaction absorb or release energy?
00
release
absorb
Can't be decided with the data given.
yes
no
☐ kJ/mol
(²) P* (8) +
+
+ e →>>
P (g)
Is it possible to calculate the amount of energy absorbed
or released by reaction (2) using only the data above?
If you answered yes to the previous question, enter the
amount of energy absorbed or released by reaction (2):
☐
release
absorb
Can't be decided with the data given.
yes
no
kJ/mol
а
Chapter 19 Solutions
Pearson eText Organic Chemistry -- Instant Access (Pearson+)
Ch. 19.1 - Name the following:Ch. 19.2 - Prob. 3PCh. 19.2 - Prob. 4PCh. 19.3 - Draw the product of each of the following...Ch. 19.5 - Prob. 6PCh. 19.5 - Explain why cyclopentadiene (pKa = 15) is more...Ch. 19.5 - When pyrrole is added to a dilute solution of...Ch. 19.6 - Prob. 10PCh. 19.6 - How to the mechanisms of the following reactions...Ch. 19.6 - Prob. 12P
Ch. 19.6 - Rank the following compounds from easiest to...Ch. 19.7 - Prob. 14PCh. 19.7 - Prob. 15PCh. 19.7 - Prob. 16PCh. 19.7 - Prob. 17PCh. 19.7 - Prob. 18PCh. 19.7 - Prob. 19PCh. 19.7 - Prob. 20PCh. 19 - Name the following:Ch. 19 - Prob. 22PCh. 19 - Rank the following compounds from strongest acid...Ch. 19 - Which of the following compounds is easier to...Ch. 19 - Rank the following compounds from most reactive to...Ch. 19 - One of the following compounds undergoes...Ch. 19 - Benzene undergoes electrophilic aromatic...Ch. 19 - Pyrrole reacts with excess...Ch. 19 - The dipole moments of furan and tetrahydrofuran...Ch. 19 - Name the following:Ch. 19 - Prob. 31PCh. 19 - Prob. 32PCh. 19 - a. Draw resonance contributors to show why...Ch. 19 - The chemical shifts of the C-2 hydrogen in the...Ch. 19 - Explain why protonating aniline has a dramatic...Ch. 19 - Prob. 36PCh. 19 - Propose a mechanism for the following reaction:Ch. 19 - Prob. 38PCh. 19 - Propose a mechanism for the following reactions:Ch. 19 - Prob. 40PCh. 19 - Prob. 41PCh. 19 - Prob. 42PCh. 19 - Organic chemists work with tetraphenylporphyrins...Ch. 19 - Show how the following compounds can be prepared...
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