Title: ???: ,??:CnH2n.
1??? ???
??????????????
2- ??? ,??CnH2n.
- ??? ?????
- ??????
CC ??610kJ/mol
3(No Transcript)
4 p-Bonding(Bonding molecular orbital)
5???????
????
?????
6??? ??????????
- ?????????
- ??????????????????????
- ????5??????
-
7?(cis)??????????????????(trans)?????
8???????
- 1. ??????????????(??),??????????????
- 2. ???????????????
- 3. ????????????,??????????????
5,5-???-1-??
9Ethene
Propene
Ethylene
Propylene
1-Butene
2-Butene
102-Methyl-2-butene
116-Methyl-2-heptene
126-Methyl-2-heptene
13??
- Ethyl CH2CH- Vinyl
- 1-Propenyl
- 2-Butenyl
- 2-Pentenyl
Allyl
Isopropenyl(for 1-methylvinyl)
14 E-Z Nomenclature
15 E-Z Nomenclature Rules
- SEQUENCE RULE 1 If the four atoms directly
attached to the double bond are all different,
priority depends on atomic number, with the atom
of higher atomic number receiving the higher
priority. - COROLLARY If two atoms are isotopes of the same
element, the heavier isotope receives the higher
priority.
16 E-Z Nomenclature Rules
- SEQUENCE RULE 2 If the relative priority of two
groups cannot be decided by Rule 1, it shall be
determined by a similar comparison of the next
atoms in the groups (and so on, if necessary),
working outward in ranks from the double bond.
17 E-Z Nomenclature Rules
- To complete the IUPAC name of a particular
isomer, enclose the (E) or (Z) symbol in
parentheses and place it at the front of the
entire name of the compound. Separate the (E) or
(Z) symbol from the rest of the name with a
hyphen.
18Examples
Question (CH3)3C-? -CH2Cl????????
19trans-6-Methyl-3-propyl-2-octene
(Dont worry about trans until Chapter 4)
20Intention
- 1. Z?E??(Cis)??(Trans)??????????
21??? ???????
- ????????--????, ? ???,??????????????????,??????,?
??????????
22Addition Reactions
23??????
??????????????Raney Ni Fe?Cr?Cu.
??????????? ????
????
24Hydrogenation of Alkenes
Also PtO2 -- sometimes Ru, Rh, or Re
25HYDROGEN ADSORBS ON THE SURFACE OF THE CATALYST
.
n H2 Pt
Pt(H )2n
finely-divided particles dispersed in solution
26MECHANISM OF HYDROGENATION
CATALYST
27MECHANISM OF HYDROGENATION
HYDROGEN ADSORBS
28MECHANISM OF HYDROGENATION
ALKENE APPROACHES
29MECHANISM OF HYDROGENATION
ALKENE PICKS UP TWO HYDROGENS
30MECHANISM OF HYDROGENATION
R
R
R
R
ALKANE IS FORMED
.
.
31???1mol???????????????
- ?????????????????
- ???????????,??????
- R2CCR2gtR2CCHRgtRCHCHRgt
- RCHCH2gtCH2CH2.
- 2-????gt?-2-??gt?-2-??gt1-???
32Alkene Stability
33??????
Electrophilic Addition to a Double Bond
????(E)??????,??????
34 351. ?????
???????????????????(???)??????????????? 1)??????
(Addition of Hydrogen Halides)
36?????????????HIgtHBrgtHCl
Markovnikov Addition to an Alkene
37 Markovnikov Addition to an Alkene
38 Markovnikov Rule
- In the ionic addition of an acid to the
carbon-carbon double bond of an alkene, the
hydrogen of the acid attaches itself to the
carbon atom which already holds the greater
number of hydrogens. - Them that has, gets!
- The richer get richer! (V. W.
Markovnikov -- 1838 - 1904)
39 REGIOSELECTIVE REACTION
???????
C
H
C
H
C
H
3
3
3
HCl
C
C
H
C
H
C
C
H
C
H
C
H
C
H
C
H
3
2
3
3
3
2
C
l
C
l
major
minor
one of the possible products is formed in larger
amounts than the other one
REGIOSPECIFIC
Compare
only one of the possible products is formed
(100).
40 MARKOVNIKOV RULE
When adding HX to a double bond the hydrogen of
HX goes to the carbon which already has the most
hydrogens
C
H
C
H
3
2
C
l
HCl
..... conversely, the anion X adds to the
most highly substituted carbon ( the carbon
with most alkyl groups attached).
41 KARASCH??(??????
????????,????????????,?????Anti-Markovnikov rule.
Reading Assignment ?????
422)?????
????????????Markovnikov rule.
???????????,???????
43Addition of Sulfuric Acid to an Alkene
44Addition of Water to an Alkene
45????
2. ?????
????????????F2gtCl2gtBr2gtI2(???)
Br/CCl4????????
ICl ? IBr???(X2H2O)????????????????
46Halohydrin Formation
??????
HOBr
473. ??????(??????B-H?????????????)?C. H. Brown??
48????????????????????,??????????????????????????
49Sia2BH,thBH2(HBH2), 9-BBN
50??
??1.??????????????2.????,????3.???4.???????
????
51?1
52??????
?-1,2-??
???????????,????????,????????????????,???????,????
?
??????,??????,????????
?KMnO4??????????
532. ???
??,?H2O2??,????????????
H2O
54????????????????
- ????????
- 1)Zn/H2O
- 2)H2,Pd
- ?????????
???????
55(No Transcript)
563.????
Organic Reaction
57??????
- ??????????????????????????????
58Polymerization of Propene
59???-H ????
60?-H????(?????)
612. ??
???
62??? ?????
- ??????
- 1. ?????HX
-
-
- 2. ??????X2
- 3. ??H2O
?-??
63Saytzeff Rule
???????
????
64??? ???????????
????
????
????????,?????????????????
65Mechanism of Bromination of an Alkene
66CYCLIC BROMONIUM ION
??????
note size of bromine
67BRIDGED BROMONIUM ION
Br
Br
Br
bridging blocks approach from this side
68BRIDGED BROMONIUM ION
-
symmetric ion - bromide ion could add to either
side left or right
B
r
H
H
B
r
-
-
B
r
B
r
H
H
H
H
B
r
B
r
resonance contributing structures
69FORMATION OF ENANTIOMERS
symmetric intermediate
Addition could also start from the top with
bromide attacking the bottom.
ENANTIOMERS
702. ???HX??
E ElectrophileNu Nucleophile General
Mechanism The first step requires a powerful
electrophile to attract the pi bond electrons,
which then forms a carbocation. A nucleophile
quickly adds to the carbocation to form the
monosubstituted product.
713. Markovnikov Rule and Stability of Carbocation
?-????
- ??
- 2)???????
- ?(3?)gt?(2 ? )gt?(1 ? )gtCH3
??-p???????
72COMPETING PATHWAYS
rate-determining step
????
higher energy intermediate
slower
faster
lower energy intermediate
rate-determininng (slow) step
73Hyperconjugation
???
H
H
C
C
H
H
H
74CARBOCATION STABILITY
HYPERCONJUGATION
????????
H
electrons in an adjacent C-H s bond help to
stabilize the positive charge of the carbocation
by proximity (overlap)
..
R
C
C
H
R
H
lowest energy
highest energy
lt
lt
tertiary
secondary
primary
754. ?????
??????
76Problem Assignment
- 1.?????????????????1,2-?????,??2-????1-?-2-???,???
? - 2.??????
77Homework Assignment
- Pp75 2.(1,3,6) 3(3,5) 568??(2)(b)?CH3CH2
CH2OH1012(???????,???????,????,???????,????) - 1315???????
- ???1820