Atkins' Physical Chemistry
11th Edition
ISBN: 9780198769866
Author: ATKINS, P. W. (peter William), De Paula, Julio, Keeler, JAMES
Publisher: Oxford University Press
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Chapter 17, Problem 17B.2AE
Interpretation Introduction
Interpretation:
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Can the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left?
?
starting
material
target
If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area.
Be sure you follow the standard ALEKS rules for submitting syntheses.
+ More...
Note for advanced students: you may assume that you are using a large excess of benzene as your starting material.
C
:0
T
Add/Remove step
G
The following equations represent the formation of compound MX. What is the AH for the
electron affinity of X (g)?
X₂ (g) → 2X (g)
M (s) → M (g)
M (g)
M (g) + e-
AH = 60 kJ/mol
AH = 22 kJ/mol
X (g) + e-X (g)
M* (g) +X (g) → MX (s)
AH = 118 kJ/mol
AH = ?
AH = -190 kJ/mol
AH = -100 kJ/mol
a)
-80 kJ
b)
-30 kJ
c)
-20 kJ
d)
20 kJ
e)
156 kJ
A covalent bond is the result of the
a)
b)
c)
d)
e)
overlap of two half-filled s orbitals
overlap of a half-filled s orbital and a half-filled p orbital
overlap of two half-filled p orbitals along their axes
parallel overlap of two half-filled parallel p orbitals
all of the above
Chapter 17 Solutions
Atkins' Physical Chemistry
Ch. 17 - Prob. 17A.1STCh. 17 - Prob. 17A.2STCh. 17 - Prob. 17B.1STCh. 17 - Prob. 17D.1STCh. 17 - Prob. 17E.2STCh. 17 - Prob. 17E.3STCh. 17 - Prob. 17F.1STCh. 17 - Prob. 17F.2STCh. 17 - Prob. 17G.1STCh. 17 - Prob. 17A.1DQ
Ch. 17 - Prob. 17A.2DQCh. 17 - Prob. 17A.3DQCh. 17 - Prob. 17A.4DQCh. 17 - Prob. 17A.1AECh. 17 - Prob. 17A.1BECh. 17 - Prob. 17A.2AECh. 17 - Prob. 17A.2BECh. 17 - Prob. 17A.3AECh. 17 - Prob. 17A.3BECh. 17 - Prob. 17A.4AECh. 17 - Prob. 17A.4BECh. 17 - Prob. 17A.5AECh. 17 - Prob. 17A.5BECh. 17 - Prob. 17A.6AECh. 17 - Prob. 17A.6BECh. 17 - Prob. 17A.7AECh. 17 - Prob. 17A.7BECh. 17 - Prob. 17A.9AECh. 17 - Prob. 17A.9BECh. 17 - Prob. 17A.1PCh. 17 - Prob. 17A.2PCh. 17 - Prob. 17A.3PCh. 17 - Prob. 17B.1DQCh. 17 - Prob. 17B.2DQCh. 17 - Prob. 17B.3DQCh. 17 - Prob. 17B.1BECh. 17 - Prob. 17B.2AECh. 17 - Prob. 17B.2BECh. 17 - Prob. 17B.3AECh. 17 - Prob. 17B.3BECh. 17 - Prob. 17B.4AECh. 17 - Prob. 17B.4BECh. 17 - Prob. 17B.5AECh. 17 - Prob. 17B.5BECh. 17 - Prob. 17B.6BECh. 17 - Prob. 17B.3PCh. 17 - Prob. 17B.4PCh. 17 - Prob. 17B.5PCh. 17 - Prob. 17B.6PCh. 17 - Prob. 17B.7PCh. 17 - Prob. 17B.8PCh. 17 - Prob. 17B.9PCh. 17 - Prob. 17B.10PCh. 17 - Prob. 17B.11PCh. 17 - Prob. 17B.12PCh. 17 - Prob. 17B.14PCh. 17 - Prob. 17B.15PCh. 17 - Prob. 17B.16PCh. 17 - Prob. 17B.17PCh. 17 - Prob. 17B.18PCh. 17 - Prob. 17C.1DQCh. 17 - Prob. 17C.2DQCh. 17 - Prob. 17C.1BECh. 17 - Prob. 17C.2AECh. 17 - Prob. 17C.2BECh. 17 - Prob. 17C.6PCh. 17 - Prob. 17D.1DQCh. 17 - Prob. 17D.1AECh. 17 - Prob. 17D.1BECh. 17 - Prob. 17D.2AECh. 17 - Prob. 17D.2BECh. 17 - Prob. 17D.3AECh. 17 - Prob. 17D.3BECh. 17 - Prob. 17D.4AECh. 17 - Prob. 17D.4BECh. 17 - Prob. 17D.5BECh. 17 - Prob. 17D.1PCh. 17 - Prob. 17D.3PCh. 17 - Prob. 17D.4PCh. 17 - Prob. 17D.5PCh. 17 - Prob. 17D.6PCh. 17 - Prob. 17E.1DQCh. 17 - Prob. 17E.2DQCh. 17 - Prob. 17E.3DQCh. 17 - Prob. 17E.4DQCh. 17 - Prob. 17E.5DQCh. 17 - Prob. 17E.6DQCh. 17 - Prob. 17E.1AECh. 17 - Prob. 17E.1BECh. 17 - Prob. 17E.2AECh. 17 - Prob. 17E.2BECh. 17 - Prob. 17E.3AECh. 17 - Prob. 17E.3BECh. 17 - Prob. 17E.4PCh. 17 - Prob. 17F.1DQCh. 17 - Prob. 17F.3DQCh. 17 - Prob. 17F.4DQCh. 17 - Prob. 17F.1AECh. 17 - Prob. 17F.1BECh. 17 - Prob. 17F.2AECh. 17 - Prob. 17F.2BECh. 17 - Prob. 17F.3AECh. 17 - Prob. 17F.3BECh. 17 - Prob. 17F.4AECh. 17 - Prob. 17F.4BECh. 17 - Prob. 17F.2PCh. 17 - Prob. 17F.3PCh. 17 - Prob. 17F.4PCh. 17 - Prob. 17F.6PCh. 17 - Prob. 17F.7PCh. 17 - Prob. 17G.1AECh. 17 - Prob. 17G.1BECh. 17 - Prob. 17G.2AECh. 17 - Prob. 17G.2BECh. 17 - Prob. 17G.3AECh. 17 - Prob. 17G.3BECh. 17 - Prob. 17G.1PCh. 17 - Prob. 17G.2PCh. 17 - Prob. 17G.7PCh. 17 - Prob. 17.3IACh. 17 - Prob. 17.6IACh. 17 - Prob. 17.7IA
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- Can the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left? starting material target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. + More... Note for advanced students: you may assume that you are using a large excess of benzene as your starting material. C T Add/Remove step X ноarrow_forwardWhich one of the following atoms should have the largest electron affinity? a) b) c) d) 으으 e) 1s² 2s² 2p6 3s¹ 1s² 2s² 2p5 1s² 2s² 2p 3s² 3p² 1s² 2s 2p 3s² 3p6 4s2 3ds 1s² 2s² 2p6arrow_forwardAll of the following are allowed energy levels except _. a) 3f b) 1s c) 3d d) 5p e) 6sarrow_forward
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