2. dong phan

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1. Đồng phân cấu tạo - Đồng phân vị trí

 ĐỒNG PHÂN ĐỒNG PHÂN

CH3CH2   NH CH2CH3   CH3CH2   N(CH32

C!H" CH2 C

#

# C2H"C!H" CH2 # C2H"C

#

CH3   C# CH2#H   H# CH2   CH2   CH#

CH3CH2CH2CH2C$   C$CH2CH(CH32

C

H

H

C$

C$ C

H

C$

H

C$

CH2 CH CH2 CH3 CH3

CH2C$CHC$CH3   CH3CHC$CH2C$

H

H% %

H H H

H% H

H %

H

H% %

H H %

H% H

H H

C&ng 1 chất

 Đp vị trí

 Đp vị trí

 Đp cấu tạo

 Đp vị trí

 Đpcấu tạo

C&ng 1 chất

C&ng 1 chất

 Đp vị trí

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2. ')t *ạng h+ ,)n

 ĐỒNG PHÂN ĐỒNG PHÂN

# H

#H

CH

N

#

C

N #H

CH3 C# CH2 C# CH3

CH3

C CH C# CH3

#H

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3. C/c h0p chất - chất n4o $4 *ạng h+ ,)n 5no$ c6

 ĐỒNG PHÂN ĐỒNG PHÂN

. 2-7utnon

CH3   C

#

CH2   CH3

#H

5   8 

#H

 9

#H

CH3

#CH3

#H

CH3

#H

,

,. 2-:5th;$c;c$oh5<non

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=. Chất n4o c> tính ?ung hoạt

 ĐỒNG PHÂN ĐỒNG PHÂN

@ @

@@

CH3 CH

#H

CH3

CH3 CH

#H

CH

7r 

CH3

CH3 CHC$

CH2 CH3

CH2 CH

CH3

CH2 CH2CH3

CH3

CH3

CH CH2 CH2 CH3CH3

CH2 CH2 CH3

CH2 C

C$

CH2C$CH3

CH3

.

,.

c.

*.

5.

8.

CH3   CH2   C

CH3

CH3

CH2   CH2   CH3

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!. H0p chất n4o c> Aồng phân cis- 

trans

 ĐỒNG PHÂN ĐỒNG PHÂN

. CH3-CHDCH-CH3

,. (CH32CDCH-CH3

c. CH3-CHDCH%

*. C%2DC%2

C CH3C

HH

CH3

C CH3C

CH3H

H

C CH3C

HH

%C C

H3C

%H

H

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!. H0p chất n4o c> Aồng phân cis- 

trans

 ĐỒNG PHÂN ĐỒNG PHÂN

5. H##C-CHDCH-C##H

8. CHC$DCDCHC$

g. CH3-CHDCDCDCH-CH3

h. CH2DCDCDCH2

. CHC$DCH-CHDCHC$

C CH##C

HH

C##H C CH##C

C##HH

H

C CC$

CH

H

C

H

H

C$

C CC$

CH

H

C

H

C$

H

C CH

CC$

H

CH

C$

H

C C C H

CH3

H

H3CC C C CH3

H

H

H3C

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  9

E. C/c h0p chất Fu c> tính ?ung hoạt Cho ,)t tng FI C ,ất AI

 ĐỒNG PHÂN ĐỒNG PHÂN

N

NCH3CH

2

O

O

O

OCH

3

CH3

CH3

N CH3

OCH3

OH

CH3 H

CH3

H

N

S CH3

CH3

HNHCCH2

O

HO

O

HOOC

d. Camphor

a. Phenobarbital b. Dextromethorphan

e. Cholesterol

c. Penicillin V

••

••

••

••

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J. ')t cKng thLc c/c Aồng phân $Mp thO cho ,)t thuc $oạ AphBnh hc h; ?ung hc

 ĐỒNG PHÂN ĐỒNG PHÂN

CH CH CH CHCH3 CH3

123="!

C CH

C

H3C

H CH

CH3H

C CH

C

H3C

H CCH3

HH

C CC

H

H3C

H

CH H

CH3

CH CH2   CH2   CHCH2   CH2

.

,. hKng c> Aồng phân $Mp th

trans, trans 2O=-h5<*5n trans, cis 2O=-h5<*5n cis, cis 2O=-h5<*5n

 Đồng phân hBnh hc 3

Ồ Â

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J. ')t cKng thLc c/c Aồng phân $Mp thO cho ,)t thuc $oạ AphBnh hc h; ?ung hc

 ĐỒNG PHÂN ĐỒNG PHÂN

CH3 CH

7r 

CH

7r 

CH3

CH3

CH3

H 7r 

7r  H H 7r 

7r  H

CH3

CH3

H 7r 

H 7r 

CH3

CH3

c.

Qhr5o R5Fo

 Đồng phân ?ung hc 1 cSp AI ?ung T 1 :5Fo

Ồ ÂỒ Â

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J. ')t cKng thLc c/c Aồng phân $Mp thO cho ,)t thuc $oạ AphBnh hc h; ?ung hc

 ĐỒNG PHÂN ĐỒNG PHÂN

*. C!H"-NDN-C!H"

 Đồng phân hBnh hcN N

C!H"

C!H

"

N N

C!H"  C!H"

anti Uo,5nU5n syn Uo,5nU5n

5. C!H"-CHDN-#H

 Đồng phân hBnh hc

anti ,5nU$o<: syn ,5nU$o<:

C N

C!H"

#HHC N

C!H

"

#H

H

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J. ')t cKng thLc c/c Aồng phân $Mp thO cho ,)t thuc $oạ AphBnh hc h; ?ung hc

 ĐỒNG PHÂN ĐỒNG PHÂN

8.

 Đồng phân hBnh hc

CH3   CH CH CH

CH3

C##H@

 Đồng phân ?ung hc

C C

H

CHH3C

H

CH3

C##HC C

H3C

CHH

H

CH3

C##H

cis trans

CH3

H

CH C##HCHCH3 H##C CH CH CH3

CH3

H

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V. Ro:5n $WXng cYc

 ĐỒNG PHÂN ĐỒNG PHÂN

. CH%DCH%   Z D [   7 D 2O=2\

1 A]; 1 h^t _ ` a

2 h^t a ` _

h^t h^t trans (_ cis (a

,. CH3CHDCH7r    Z D 1O"E   7 D 1O!V\

A]; h^t cis (a trans (_

 Z D 3O11\   7 D =O"2\

h^t h^t trans (_ cis (a

#2N CH CH 7r  c.

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11. Đc cấu hBnh b

 ĐỒNG PHÂN ĐỒNG PHÂN

12

3

1

23

1

2

3

12. Đc cấu hBnh b c6 ch$or:ph5nco$

CH2OH

OH H

H NH   CO CHCl2

NO2

1

2

3

12

3

CH3

C##HH

7r 

#H

C##HH3C

H

NH

2CH3H

CN

.   ,.   c.

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13. QrBnh ,4; cKng thLc ch)u %Fh5r 

 ĐỒNG PHÂN ĐỒNG PHÂN

CH3

H

CH2#H

#H H CH3

CH2#H

#H

CH2#H

H

H# CH3

. Propn*o$-1O2

,. 2-ch$oro-3-,ro:o,utnCH3

CH3

H C$

H 7r H C$

CH3

d

CH3

H

d C$

CH3 7r 

d

H

d

CH3

H 7r 

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1". QrBnh ,4; c/c th ,en Lng vf c/c Aồng phân th) c6 c;c$oh5<n

 ĐỒNG PHÂN ĐỒNG PHÂN

55

5

55   5

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