Chem 125 Review 12/14/05 Projected material This material is for the exclusive use of Chem 125...
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![Page 1: Chem 125 Review 12/14/05 Projected material This material is for the exclusive use of Chem 125 students at Yale and may not be copied or distributed further.](https://reader031.fdocuments.in/reader031/viewer/2022032310/56649d645503460f94a46d9a/html5/thumbnails/1.jpg)
Chem 125 Review12/14/05
Projected material
This material is for the exclusive use of Chem 125 students at Yale and may not
be copied or distributed further.
It is not readily understood without reference to notes from the lecture.
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Functional Group Names
RED: Memorize & Identify HOMO/LUMO
BLUE: Memorize
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Substitution of Cl for H• •
H CH3Cl Clweak bond
(58 kcal/mole)
••
SOMO
H Cl
•
CH3 Cl Cl
CH3Cl
•
Cl
single-electrons
single-barbedarrows
"free-radical chain"
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Cl Cl*
C
CH2
H2
••
+*n
+
Addition of Cl2 to an Alkene
ClC
CCl
H2
H2
C
C
H2
H2Cl
ClCl(actually both
steps at once)
••
••HOMO() LUMO(*)HOMO(p)
LUMO(p)
New LUMONew HOMO-2New
HOMO-1
NewHOMO
* F-CH3
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It is very common for an “electrophile” (LUMO) adding to the HOMO of an alkene to come along with a HOMO that can react
with the * LUMO of the same alkene. This is the case in the previous example where the
LUMO is the * of Cl-Cl (or the vacant 2p orbital of Cl+) and the
HOMO is an unshared pair of Cl.
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EthersHOMO :O
LUMO *CO
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Alkyl Halides AlcoholsHOMO :XLUMO *CX
HOMO :OLUMO *OH
(or *CO)
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Aldehydes / Ketones
R
R
O
-Y:
R R
O
Y
-
Addition of HY to C=O
H__Y
-Y:R R
OH
Y
HOMO :OLUMO *C=O
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Imines BoranesLike C=OHOMO :NLUMO *
HOMO B-H
LUMO 2pB
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Carboxylic Acids
Acidic because RCOO- has better HOMO-LUMO mixing
(resonance stabilization) than RCOOH.
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Acid Derivatives
All have an X group attached to C=O that can leave as a reasonable anion.
R
X
O
-Y:
R X
O
Y
-
R
Y
O
X-
reverse or Substitution of Y for X
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I think I have fixed the following frame from the lecture of
11/16/05 so that it works with other browsers.
[No one had told me of the problem until day before yesterday. Let me
know when something fails.]
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CIP (R/S) Nomenclaturefor Stereogenic Centers
(S)inister (left)
COOH
COOH
OH
H
H
HO4
3
2
1
1
3
4
2
(2R,3R)-2,3-dihydroxybutanedioic
acid
rightturn
H
(R)ectus (right)
H
Jones Sec. 4.4 pp. 157-161
HO D
CH3
H
leftturn
HO CH3
D
H
14
2
3
CH3 CH3
HO HODHHD
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Why Maxwell’s velocity distributions are different in
1, 2, and 3 Dimensions.
(a minor point for Chem 125)
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James Clerk Maxwell
(1831-1879)
Distributionof Velocities
On the Motions and Collisions of perfectly elastic Spheres (1859)
to find: f(vx)
probability ofx-velocity between
vx and vx + d vx
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vx
vz
vy
v
(Total velocity) v2 = vx2 + vy
2 + vz2
Assume vx , vy , vz are independent
(meaning that joint probability is a product)
g(vx2 + vy
2 + vz2) = f(vx) f(vy) f(vz)
ProductSum
g(vx2 + vy
2 + vz2) = c3 e-a (vx
2 + vx2 + vx
2)
f(vx) = c e-a vx2
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f(v) = C v2 e-a v2
vx
vz
vy
v
Note that for a certain magnitude of v, the little dx dy dz box, in which we have reckoned probability, could be anywhere on the surface of a sphere of radius v. The area of this surface is proportional to v2.
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f(v) = C v2 e-a v2
0.00
0
v
f(v)
1D2D
3D
MaxwellVelocity
Distribution