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CH3COOCH2
CH2CH2CH3
C C
H
H
cis-
CH3COOCH2
H
C C
H
CH2CH2CH3
trans-
*Dng trans- c nhit nng chy cao hn do cu trc tinh th ca dng trans- bn vng sp xp cht kht hn so
vi dng cis- (dng trans- vn gi nguyn cu trc zic-zac ca mch cacbon, dng cis- ph v cu trc zic-zac ny).
Bi 2: Di y l cc gi tr nhit nng chy v nhit si ca n-pentan v neopentan. Gii thch s khc bit
nhit nng chy v nhit si gia cc cht ny.
n-Pentan Neopentan
Nhit si (oC)
36
9,5
Nhit nng chy (oC)
-130
-17
* Nhit si ca neopentan thp hn n-pentan v khi phn t c cng nhiu nhnh, tnh i xng cu ca phn t
cng tng, din tch b mt phn t cng gim, lm cho bn tng tc lin phn t gim v nhit si tr nn
thp hn.
* Tri li, tnh i xng cu li lm cho mng tinh th cht rn tr nn c kht hn v bn vng hn, nn nhit
nng chy cao hn.
Bi tp 3: So snh v gii thch vn tt:
(a) Nhit si ca pentan-1-ol, 2-metylbutan-2-ol v 3-metylbutan-2-ol.
(b) Tnh tan trong nc ca pentan-1,5-diol v pentan-1-ol
(c) mnh tnh axit ca CH4, C6 H5OH, CH3OH, CH3COOH, CH3SO2OH
Gii: (a) Trt t tng dn nhit si:
CH3
OH
C CH2 CH3
CH3
CH3 CH CH CH3
CH3 OH
CH3CH2CH2CH2CH2OH
Khi s mch nhnh tng th cu trc c xu hng thu gn tr thnh dng cu, lm gim bn lin kt lin phn t.
(b) pentan-1,5-diol tan tt hn pentan-1-ol, do c nhiu nhm -OH to c lin kt hidro a phng, a chiu hn.
-1-
O H
CH3-H
CH3O-H
O H CH
3
CH3
O
khng
phn
cc
phn cc yu
do CH3- y
electron
CH3-
CH3O-
phn cc mnh do
C6H5- ht electron
O
phn cc mnh
nht do c hai
nhm SO ht
electron
phn cc mnh
hn do CO ht
electron mnh
hn
O 1/3-
1/2-
O-
O
CH3
CH3
1/2-
km bn,
khng c gii
ta in tch
bn do c s gii
ta in tch
S O 1/3O 1/3-
O
km
bn
S O H
bn do c s gii
ta in tch trn
hai O
bn do c s gii
ta in tch trn
ba O
HO
OH
C C
O-
HO
C C
O 2-
O
C C
O
O
-
-2-
BI TP RN LUYN
Cu 1: Nhit si ca cc cht CH3CHO, CH3COOH, CH3CH2COOH, CH4 c sp xp theo chiu tng dn l :
A. CH3CHO, CH3COOH, CH3CH2COOH, CH4 . B. CH3COOH, CH3CHO, CH3CH2COOH, CH4 .
C. CH4, CH3CHO, CH3COOH, CH3CH2COOH . D. CH3CHO, CH3CH2COOH, CH3COOH, CH4 .
Cu 2: Nhit si ca cc cht c sp xp theo th t tng dn :
A. C 2H5Cl < CH3 COOH < C2H5OH .
B. C2H5OH < C2H5Ci < CH3COOH .
C. C2H5Cl < C2H5OH < CH3COOH .
D. CH3COOH < C2H5OH < C2H5Ci .
Cu 3: Cht c nhit si cao nht l :
A. CH3COOH
B. CH3CHO
C. C2H5OH
D. CH3COCH3
Cu 4: Nhit si ca cc cht : (1) axit fomic ; (2) anehit fomic ; (3) ru metylic . c xp theo th t tng
dn l :
A. 1, 2, 3
B. 2, 1, 3
C. 2, 3, 1
D. 3, 2, 1
Cu 5: Trong cc cch sp xp tng dn nhit si ca cc cht sau, th t ng l:
A. HCOOCH3 < CH3COOCH3 < n- C3H7OH < CH3COOH < C2H5COOH
B. HCOOCH3 < CH3COOH < n- C3H7OH < CH3COOCH3< C2H5COOH
C. HCOOCH3 < CH3COOCH3 < CH3COOH < n- C3H7OH < C2H5COOH
D. n- C 3H7OH <HCOOCH3 < CH3 COOH < C2H5COOH < CH3COOCH3
Cu 6: Cc cht sau c sp xp theo chiu tng nhit si l :
A. ru etylic, anehit axetic, axit axetic, ru metylic .
B. anehit axetic, ru metylic,ru etylic, axit axetic.
C. ru metylic,ru etylic, axit axetic, anehit axetic.
D. axit axetic,ru metylic,ru etylic, anehit axetic.
Cu 7: Trong dy ng ng ca ru no n chc khi mch cacbon tng ni chung:
A. si tng , kh nng tan trong nc tng .
B. si gim , kh nng tan trong nc gim .
C. si tng , kh nng tan trong nc gim .
D. si gim , kh nng tan trong nc tng .
Cu 8: Trong hn hp etanol v phenol lin kt hiro bn hn c l :
A. O - H ... O - H
B. O - H ... O - H
C2H5
C2H5
C. O - H ... O - H
C2H5
C6H5
D. O - H ... O - H
C6H5
C6H5
C6H5
C2H5
-3-
OH
OH
OH
OH
OH
A. (1) < (2) < (3);
C. (1) < (3) < (2);
OH
|
CH3
D. C A, B, C
D. khng so snh c
Cu 22: Nhit si ca ru etylic (1), ru metylic (2), axeton (3) dimetyl ete (4) xp theo trt t gim dn l:
A. (1) > (2) > (3) > (4)
Cu 23: Ru etylic (1), etyl bromua (2) v etan (3), trt t v tan trong nc gim dn l:
A. (1), (3), (2)
Cu 24: So snh nhit si ca cc cht sau Ru etylic (1) , etyl clorua (2), ietyl ete (3) v axit axetic (4) ta
c:
A. (1 ) > (2) > (3) > (4)
-4-
Cu 28: .Cho 4 cht: X(andehit fomic), Y (axit axetic), Z (ru metylic), T (axit fomic). Nhit si c sp theo
th t tng dn nh sau:
A. Y < Z < X < T
B. X < Z < T < Y
C. Z < X < Y < T
D. X < Z < Y < T
Cu 29:. Cho cc cht : CH3CHO, CH3COOH, HCOOCH3 , CH3 CH2OH.
Cht c nhit si cao nht l :
A. CH3CHO
B. CH3COOH
C.HCOOCH3
D. CH3CH2OH
Cu 30: Dy sp xp theo th t tng dn nhit si ca cc hp cht c cng s nguyn t cacbon
A. Ankan, axit, anehit, ancol.
B. Anehit, ankan, ancol, axit.
C. Ankan, anehit, axit, ancol.
D. Ankan, anehit, ancol, axit.
Cu 31:. Trong dung dch, axit cacboxylic c lin kt hiro v c th :
A. dng polime.
B. dng ime.
C. to lin kt hiro vi nc.
D. C A, B, C.
Cu 32: Lin kt H no sau y biu din sai ?
A. ... O H ... O C 2 H5
|
C 2 H5
C.
Cu 33:
B. ... O H ... O H
|
C 2 H5
|
C 2 H5
HO ... H O
|
|
CH2
CH2
|
C 2 H5
D. H - C - OH .... H - C - OH
||
O
||
O
A. CH3 - CH2 - OH
C. CH3 - CH2 - Cl
D. CH3 - COOH
Cu 35: Sp xp theo chiu tng dn nhit si cc cht : p-nirophenol (1), phenol (2), p- crezol(3).
A. (1) < (2) < (3)
Cu 36: Cho cc cht : p-NO2C6H4 COOH (1), m-NO2 C6H4 COOH (2), o-NO2C6H4 COOH (3)
Tnh axit tng dn theo dy no trong s cc dy sau y ?
A. (2) < (1) < (3)
B. Anehit propionic
C. Axeton
D. Axitpropionic.
Cu 40: Nhit si ca C4H10 (1), C2H5 NH2 (2), C2H5OH (3) tng dn theo th t:
A. (1) < (2) < (3)
B. (1) < (3) < (2)
C. (2) < ( 3) < (1)
D. ( 2) < ( 1) < (3)
Trong cc cht sau, cht no tan trong nc nhiu nht ?
A. C 6H6
B. C2H5Br
C. C2H5OH
D. C6H5-CH3
Cu 41: Sp xp cc hp cht sau theo th t tng dn nhit si: axit axetic (1), ru n-propylic (2), ru
isopropylic (3), metyl etyl ete (4):
A. (1) < (2) < (3 ) < (4)
B. (4) < (3) < (2) < (1)
C. (1) < (4) < (3) < (2)
-5-
CH3COOH (2) ,
HCOOH (3) ,
Cu 43: Sp xp cc hp cht: CH3COOH, C2H5OH v C6H5OH theo th t tng axit. Trng hp no sau y ng
A. C2H5OH < CH3 COOH < C6H5OH
Cu 44: Sp xp cc hp cht: CH3COOH, C2H5 OH v C6H5OH theo th t tnh axit tng dn. Trng hp no sau
y ng?
A. C 2H5OH < CH3COOH < C6H5OH
C. CH3COOH < C6H5 OH < C2H5OH
B. CH3COOH
C. CBr3COOH
D. CF3COOH
Cu 46: .Cho 4 axit: CH3COOH, H2CO3, C6H5OH, H2SO4. mnh ca cc axit c sp theo th t tng dn
A. CH3COOH < H2CO3 < C6H5OH < H2SO4 B. H2CO3 < C6H5OH < CH3COOH < H2SO4
C. H2CO3 < CH3COOH < C6H5OH < H2SO4 D. C6H5OH < H2CO3 < CH3COOH < H2SO4
Cu 47: . mnh baz xp theo th t tng dn ng trong dy no:
A. CH3-NH2 , NH3 , C2H5NH2 , C6H5NH2
Cu 48: . Cho cc cht: (C6 H5)2NH , NH3 , (CH3)2NH ;C6 H5NH2 . Trt t tng dn tnh baz (theo chiu t tri qua
phi) ca 5 cht trn l
A. (C6H5)2NH , C6H5NH2 ; NH3 , (CH3)2NH ;
Cu 49: Cho cc cht sau: C6H5 NH2 (1) , C2H5NH2 (2); (C2H5)2NH (3) ; NaOH (4) ; NH3 (5)
Trt t tng dn tnh baz (t tri qua phi) ca 5 cht trn l :
A. (1), (5), (2), (3), (4)
Cu 50: Hy sp xp cc cht sau y theo trnh t tnh baz tng dn t tri sang phi: amoniac, anilin, pnitroanilin, metylamin, imetylamin.
A. O2 NC6H4NH2 < C6H5NH2 < NH3 < CH3NH2 < (CH3)2NH
B. C6H5NH2 < O2NC6H4NH2 < NH3 < CH3NH2 < (CH3)2NH
C. O2NC6H4NH2 < C6H5NH2 < CH3NH2 < NH3 < (CH3)2NH
D. O2NC6H4NH2 < NH3 < C6H5NH2 < CH3NH2 < (CH3)2 NH
Cu 51: . Sp xp cc amin : anilin (1), metyl amin(2), imetyl amin(3) v trimetyl amin (4) theo chiu tng dn tnh
baz
A. (1) < (2) < (3) < (4) B. (4) < (1) < (3) < (2)
C. (1) < (2) < (4) < (3) D. (1) < (4) < (3) < (2)
Cu 52: Anilin t tan trong :
A. Ru.
B.Nc.
C. Ete.
D. Benzen.
Cu 53:. Dy no sp xp cc cht theo chiu tnh baz gim dn ?
A. NH3 , CH3NH2, C6 H5NH2, (CH3)2NH B. CH3NH2, (CH3)2NH, NH3, C6H5NH2
C. C6H5NH2, NH3, CH3NH2, (CH3)2NH D. (CH3)2NH, CH3NH2, NH3, C6H5NH2
Cu 54: Dy no sp xp cc cht theo chiu tnh baz gim dn ?
A. H2 O, NH3, CH3NH2, C6H5NH2
B. C6H5NH2, NH3, C6H5NH2, H2O
-6-
Cu 57: linh ng ca nguyn t H trong nhm OH ca cc cht C2H5OH, C6H5OH, HCOOH v CH3COOH tng
dn theo trt t no ?
A. C 2H5OH < C6H5OH < HCOOH < CH3COOH. B. CH3COOH < HCOOH < C6H5OH < C2H5OH.
C. C2H5OH < C6H5 OH < CH3COOH < HCOOH.
Cu 60: Sp xp theo th t tng dn tnh axit : H3CH2COOH (1), CH2=CHCOOH (2), CHCCOOH(3).
A. (1) < (2) < (3)
B. CH3COOCH3
(2) C2H5NH2
-7-
(5) NaOH
(6) NH3
A. (1) > (3) > (5) > (4) > (2) > (6)
B. (5) > (6) > (2) > (1) > (2) > (4)
C. (5) > (4) > (3) > (5) > (1) > (2)
D. (5) > (4) > (2) > (6) > (1) > (3)
(4) H 2 N CH 2 CH 2 CH COOH
|
NH2
|
NH2
A. (2), (4)
B. (3), (1)
C. (1), (5)
D. (2), (5).
X2 : CH3 - NH2
X5 : H 2 N CH 2 CH 2 CH 2 CH COOH
|
NH2
|
NH2
B. X2, X3, X4
C. X2, X5
D. X1, X3, X5
C. CH3CH2CH2NH2
B. CH3CC-NH2
D. CH3CH2NH2
Cu 71: Cho cc cht sau : CH3CH2NHCH3(1), CH3CH2CH2NH2(2), (CH3)3N (3). Tnh baz tng dn theo dy :
A. (1) < (2) < (3)
Cu 73; Cho cc cht sau : p-NO2C6 H4NH2 (1), p-ClC6H5NH2 (2), p-CH3 C6H5NH2 (3).
Tnh baz tng dn theo dy :
A. (1) < (2) < (3)
B. C6H5NH2
C. CH3-CH2-CH2 -NH2
D. CH3-CH(CH3)-NH2
C. Nguyn t N c m in ln
-8-
-9-
- 10 -
D. (I) v (II)
- 11 -
(d) p-O2NC6H4NH2 .