Professional Documents
Culture Documents
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Trang: 1
a.
M t cc trung tm lp th ca Streptimidon bng k hiu E, Z v R, S.
b.
Streptimidon c bao nhiu ng phn lp th, trong c bao nhiu ng phn enan v bao
nhiu ng phn dia.
Cu 2: So snh v gii thch:
a. Nhit si ca cc cht sau: xyclopentan, tetrahirofuran v piroliin.
b. mnh tnh baz ca: imetylamin, piperiin v piriin
Cu 3: Cht ()Nicotin l mt loi ankaloit c trong thuc l v c th c tng hp theo cch sau:
to
(1) Axit nicotinic (3-pyridincacboxylic) + SO2Cl2
nicotinyl clorua (C6H4ONCl)
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4
2
H 5C 6
HO
O
8
O O
3
4
2
O
5
O
1
C 6H 5
OH
H 5C 6
HO
Trang: 2
O
9
C6H5
OH
Cu 6: Dng mi tn cong ch r c ch chuyn 7-ehirocholesterol (I) thnh vitamin D3 (II) v cho bit cu
dng bn ca n. Bit trong cng thc di y: R l: -CH(CH3)-(CH2)3-CH(CH3)2
R
(II)
(I)
HO
HO
Hng dn gii:
2.
R
H
H2C
as
HO
HO
to
R
HO
HO
CuCu
dng
bnbn: S-trans
dng
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Trang: 3
CH3
O
CH3
H3C
CH3
CH3
2. a.
B (C10H20O2)
- H2O
A (C10H18O)
H
H2O
OH
B
Gi tn B: 1-hiroxi-4-(-1-hiroxi-1-metyletyl)-1-metylxiclohexan
b. Dng cng thc cu trc, vit phng trnh phn ng v trnh by c ch y ca phn ng.
C 2 dng trans v cis ca B u cu dng gh bn vng, tuy vy cu dng gh khng th tham gia ng
vng m phi i qua dng thuyn km bn. Dng thuyn s tham gia phn ng SN1 ni phn t.
OH
(+)
OH
OH
OH OH
OH
(+)
Cis-B
(+)
OH
OH
OH
OH
OH
Trans-B
OH
(+)
+
2 H2O
OH
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4.
HO
Cl
H2O
HCl
Trang: 4
D
H+
(+)
Cl-
Chuyn v
chuyn v
(+)
H2N-N
NH
NH
S
S
(II)
(I) O
Hng dn gii:
1. Trong li ng v v tru c cha pentozan,khi un nng vi dung dch HCl 12% chuyn thnh pentoz
ri tch nc cho fufurol
CHO
- 3H2O
(CHOH)3
CH2OH
2
O A
O
b.
O
CHO
KOH
O C
COOK
H3O+
A(C5H4O2)
COOK
COOH
B
COOH +
CH2OH
CHO
CH2OH
H+
COOCH2
CHO
(CH3CO)2O
CH(OCOCH3)2
Thc hin phn ng nitro ho, sau thu phn phc hi nhm CHO
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CH(OCOCH3)2
O
d.
HNO3
O2N
CH(OCOCH3)2
H3O+
O2N
Trang: 5
CHO
D
Phn ng ca D vi I v II
O2N
D
I
O
O2N
H2N N
CHO
CHO
O2N
NH
NH
O2N
CH
N N
CH
O
NH
NH
II S
Cu 9: Geniposit (hnh di) l mt hp cht c tch ra t qu dnh dnh. Thu phn geniposit sinh ra hai
sn phm l genipin v D-glucoz. Genipin tham gia phn ng to mu vi gelatin (y l c s pht hin
du vn tay trong k thut hnh s). Hy vit s phn ng to genipin v phn ng ca genipin vi mt
aminoaxit gii thch hin tng trn.
COOCH3
HOH2C
HO
HO
O
O
O
OH
CH2OH
Hng dn gii:
Phn ng thu phn geniposit thu c genipin v D-glucoz
COOCH3
COOCH3
OH
O
HOH2C
O
HO
HOH2C
HO
OH
HO
OH
OH
CH2OH
HO
OH
Gelatin (c trong da) cu to t cc polipeptit, ly i din l mt aminoaxit nh glyxin, ta c phng trnh:
COOCH3
COOCH3
H2N-CH2-COOH
N-CH2-COOH
HOH2C
HOH2C
OH
OH
sn phm c mu pht hin du vn tay trong k thut hnh s.
Cu 10: Ngi ta phn lp c mt tetrapeptit (peptit A) t prothrombin ngi. Cu to ca peptit A
c tin hnh xc nh nh sau:
a. Bng phng php Edman th nhn c trnh t aminoaxit ca peptit A l Leu-Glu-Glu-Val.
b. tip tc xc nh cu to, ngi ta tin hnh in di trn giy pH 6,5 peptit A v mt peptit tng
hp B (cng c trnh t aminoaxit l Leu-Glu-Glu-Val) th li nhn c qung ng di chuyn khng
ging nhau, c th nh hnh di y:
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Peptit A
Trang: 6
2,5
Peptit B
1,7
0
1
2
3
n v di
o
c. Khi thu phn hai peptit A v B bng HCl 6N 110 C, th c A v B u cho Leu(1), Glu(2), Val(1) ; nhng khi
thu phn bng kim th peptit B cho Leu(1), Glu(2), Val(1) cn peptit A cho Leu(1), X(2), Val(1).
Hy gii thch cc kt qu thc nghim xc nh cu to ca X v gi tn X theo danh php IUPAC.
Hng dn gii:
1. Xc nh cu trc ca X
- Phng php Edman thc hin pH thp,bit c trnh t l Leu-Glu-Glu-Val.
- in di pH 6,5 cho thy peptit A dch chuyn nhanh hn v pha cc dng(+), chng t A c in
tch m ln hn B,tnh axit ca A ln hn B.
- Khi thu phn trong mi trng HCl 6N 110oC th c A v B u thu c Leu(1), Glu(2) v Val(1). Kt hp vi phng php Edman trn cho thy cc qu trnh ny thc hin mi trng axit mnh, pH
thp. pH thp phn t X b ecacboxyl ha, loi CO2 mt i 1 nhm COOH.
- Khi thu phn bng kim peptit A to ra Leu(1),X(2) v Val(1),trong mi trng kim khng c qu trnh
decacboxyl ho nn nhn c X(2).
- Kt hp cc kt qu trh nghim cho thy X c thm 1 nhm COOH so vi Glu tc l khi loi 1 nhm
COO th X chuyn thnh Glu.
X
HOOC CH2 CH2 CH COOH
CO2
NH2
Vy X l::
Vy X
HOOC CH CH2 CH COOH
NH2
COOH
Gi tn: Axit 3-aminopropan-1,1,3-tricacboxylic
Cu 11: Vit s phn ng oxi ha D-glucoz to thnh axit anonic v axit anaric, cng thc Haworth
cc mono v i -lacton ca chng v gi tn cc lacton y.
Hng dn gii:
O
COOH
CHO
OH
OH
HO
OH
OH
CH2OH
HNO3
COOH
OH
HO
OH
OH
COOH
Br2
HO
H2O
OH
O
OH
OH
OH
D- -gluconolacton
OH
HO
CH2OH
CH2OH
axit gluconic
COOH
OH
O
CH2OH
OH
O
OH
OH
COOH
O
OH HO
OH
O
O
O
O
O
OH
1,4-lacton ca axit glucaric
1,4:3,6-dilactonca axit glucaric
3,6-lactonca
caaxit
axit glucaric
glucaric
3,6-lacton
OH
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Trang: 7
CH3C=O
C2H5
1.
H
(A)
C6H5MgBr
2.
H2O
HBr a
c
C3H7
a. Viet c che phan ng va cong thc cau tao cac san pham.
b. Goi ten cac cau hnh cua B v C theo danh phap R, S.
Cu 13: Hay giai thch s hnh thanh nhanh chong 2,4,6-Br3C6H2NH2 (C) khi cho pH2N-C6H4-SO3H (A) hoac p-O2N-C6H4-COOH (D) tng tac vi dung dch nc
brom.
Cu 14: Lam the nao thc hien chuyen hoa sau vi hieu suat tot nhat:
C
NH2
NH2
H2N-NH2
t0
H (C5H8N2)
NaOEt, HOEt I
NaOEt, HOEt K (C15H22O7)
d. EtOOCCH2COOEt + 2CH2=CH-COOEt
t0
e. EtOOCCH2COOEt + H2N-CO-NH2
L (C4H4N2O3)
C khong 100 ancaloit piroliziin khc nhau c phn lp, trong c retronexin
ln u tin c tch ra t thc vt vo nm 1909, nhng mi n nm 1962 mi c
tng hp trong phng th nghim theo s sau:
EtOOC(CH2)2NHCOOEt
B (C14H21O7N)
E (C6H10O2NCl)
H (C10H17O4N)
O
D
ietyl fumarat
1. HCl
2. HOEt, HCl
C (C11H17O5N)
BrCH2COOEt, Na2CO3
1. H2O, OH , t
2. H+
NaOEt
A (C16H27O8N)
NaBH4
F (C10H15O4N)
D
KOEt
1. HOEt, H+
2. LiAlH4, THF
3. H2O
I (C8H11O3N)
O
N COOEt
Na
1. H2O, OH -, t0
2. HCl
H2, Pt
G
HO
CH2OH
HO H COOEt
N
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Trang: 8
NaBH4 (2)
(1)
p-Benzoquinon (C6H4O2) + Axit (E)-penta-2,4-ienoic
A (C11H10O4)
C
H
COOOH
(3)
(CH
CO)
O
(4)
6 5
3
2
B (C11H12O4)
C (C11H12O5)
D (C11H10O4)
C9H17N
MeCOCMe2CHO
H
(D cha 1 nguyn t Clo trong phn t, H c ng phn Cis-trans. Cc sn phm D,
E, G, H u l sn phm chnh)
a. Vit cng thc cu to ca A, B, C, D, E, G, H v vit cc phng trnh phn ng
xy ra.
b. So snh nhit nng chy ca B v C. Gii thch.
Cu 21: Hp cht hu c A c cng thc phn t C7H9N. Cho A phn ng vi C2H5Br (d),
sau vi NaOH thu c hp cht B c cng thc phn t C11H17N. Nu cng cho A
phn ng vi C2H5Br nhng c xc tc AlCl3 (khan) th to ra hp cht C c cng cng
thc phn t vi B (C11H17N). Cho A phn ng vi H2SO4 (c) 180oC to hp cht D
c cng thc phn t C7H9O6S2N, sau khi ch ho D vi NaOH 300oC ri vi HCl s cho
sn phm E (E c phn ng mu vi FeCl3). Mt khc, nu cho A phn ng vi NaNO2
trong HCl 5oC, ri cho phn ng vi -naphtol trong dung dch NaOH th thu c
sn phm c mu G.
Xc nh cng thc cu to ca A, B, C, D, E, G v vit cc phng trnh phn ng
(nu c) minh ho.
Cu 22: Amyglain (k hiu l A) c cng thc phn t C20H27O11N l mt isaccarit
thin nhin khng c tnh kh, ch cha lin kt -glicozit.
- Khi thu phn A bng dung dch axit long th thu c glucoz v hp cht B
(C7H6O) lm mt mu nc brom.
- Khi un A vi dung dch axit c th thu c glucoz v hp cht C (C8H8O3).
Oxi ho C bng dung dch KMnO4 ri axit ho th thu c D (C7H6O2) khng lm
mt mu dung dch nc brom.
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Trang: 9
Cho A tc dng vi CH3I ly d (mi trng kim), thu phn (mi trng axit), ri cho
cc sn phm tc dng vi HIO4 (d) th thu c 2,3,4,6-tetra-O-metylglucoz ; 2,3imetoxibutanial v metoxietanal.
a. Hy xc nh cng thc cu to ca A, B, C, D.
b. Hy gii thch s to thnh B khi thu phn A. Hp cht C c quang hot
khng? V sao?
Cu 23: Epiclohidrin la mot epoxit, nguyen lieu chnh e che tao nha epoxi
dung lam keo dan kim loai, knh, sanh s. Epiclohidrin phan ng vi
C6H5MgBr tao thanh C6H5CH2CH(OH)CH2Cl.
a. Xac nh cong thc cau tao cua epiclohidrin.
b. Viet cac phng trnh phan ng khi cho epiclhidrin tac dung vi ru
etylic, dung dch NH3 va khi epiclohidrin b thuy phan trong moi trng
kiem.
c. e ieu che nha epoxi, ngi ta un nong epiclohidrin vi bisphenol-A.
Viet phng trnh phan ng. Bisphenol-A l (2,2-bis-[p-hidroxiphenyl] propan.
d. Khi tron nha epoxi noi tren vi mot amin a chc v du nh vi
N(CH2CH2NH2)3 th se thu c polime mang khong gian. Giai thch.
Cu 24: Axit fumaric v axit maleic c cc hng s phn li nc 1 (k1), nc 2 (k2).
Hy so snh cc cp hng s phn li tng ng ca hai axit ny v gii thch.
Cu 25: Cho cc ancol sau: p-CH3-C6H4-CH2OH , p-CH3O-C6H4-CH2OH, p-CN-C6H4-CH2OH v
p-Cl-C6H4-CH2OH..
So snh kh nng phn ng ca cc ancol vi HBr v gii thch.
Cu 26: Oxi ho hirocacbon thm A (C8H10) bng oxi c xc tc coban axetat cho sn phm B. Cht B c
th tham gia phn ng: vi dung dch NaHCO3 gii phng kh CO2; vi etanol (d) to thnh D ; un nng
B vi dung dch NH3 to thnh E. Thu phn E to thnh G, un nng G nhit khong 1600C to thnh F.
Mt khc, khi cho B phn ng vi kh NH3 (d) cng to thnh F.
Hy vit cc cng thc cu to ca A, B, D, G, E v F.
Cu 27: Hp cht 2,2,4-trimetylpentan (A) c sn xut vi quy m ln bng phng php tng hp xc
tc t C4H8 (X) vi C4H10 (Y). A cng c th c iu ch t X theo hai bc: th nht, khi c xc tc axit
v c, X to thnh Z v Q; th hai, hiro ho Q v Z.
a.
Vit cc phng trnh phn ng minh ha v tn cc hp cht X, Y, Z, Q theo danh php IUPAC.
b.
Ozon phn Z v Q s to thnh 4 hp cht, trong c axeton v fomanehit, vit c ch phn ng.
Cu 28: Cho s cc phn ng sau:
OH
HCHO
OH -
A NaCN
DMF
H2O
Cl
Trang: 10
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CH3OH/H
B HIO4
1. LiAlH4
2. H2O
Br2/H2O
H2O/H
H2O/H
HOCH2-CHO + HOCH2-CH2OH
CHO-COOH + HOCH2-COOH
V cu trc ca B, C, D v E.
Cu 33: Hp cht A (C4H6O3) quang hot, khng tham gia phn ng trng bc, tc dng vi anhirit axetic
to ra dn xut monoaxetat. Khi un nng vi metanol, A chuyn thnh cht B (C5H10O4). Di tc dng
ca axit v c long, B cho metanol v C (C4H8O4). C tc dng vi anhirit axetic to ra dn xut triaxetat,
tc dng vi NaBH4 to ra D (C4H10O4) khng quang hot. C tham gia phn ng trng bc to thnh axit
cacboxylic E (C4H8O5). X l amit ca E bng dung dch long natri hipoclorit to ra
D-(+)glyxeranehit (C3H6O3) v amoniac. V cu trc ca A, B, C, D v E.
Cu 34: Xc nh cc cht t A n G v hon thnh cc phng trnh phn ng trong chui bin ha sau:
o
1.CH 3 MgCl
H 2SO4 ,t
H 2SO 4 ,t
C6 H12O(A)
C 6H 10(B)
C 6H 12O(D)
2.H O+
3
KMnO (c nng)
4
H Pt
2
1. CH MgCl
/
Metyl xiclopentan
C10H16 (G)
2. H3O+
C10H18O (F)
1.Mg,ete
HBr
C5H 9Br(E)
2. Xiclopentanon
C6 H 5COOOH
C5H8O (C)
3.H 3O +
NH3CH2COOH
(A)
K12
(B)
NH2CH2COOH K21
(C)
(B')
1. Vit phng trnh biu th mi quan h gia cc hng s cn bng
2. Tnh im ng in pHI ca glyxin bit: pK1 = 2,35 ; pK2 = 9,78
3. Biu th mi quan h gia:
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a. K1 vi K11 v K22
b. K2 vi K21 v K22
Cu 40: Hp cht thin nhin X c cng thc phn t C7H14O6 l mt cht khng c tnh kh v khng t
ng phn ha c. Thy phn X bng HCl long thu c cht Y (C6H12O6) l mt monosaccarit c tnh
kh. Oxi ha Y bng HNO3 long, nng thu c mt iaxit M (C6H10O8) khng c tnh quang hot. Lm
gim mch ca monosaccarit Y chuyn nhm CH(OH)CHO thnh nhm CHO (thoi phn Ruff) th
thu c monosaccarit Z (C5H10O5). Z b oxi ha bi HNO3 long, nng cho iaxit N (C5H8O7) c tnh
quang hot. Cho X tc dng vi CH3Br trong mi trng baz sinh ra P. Cht P tc dng vi dung dch
HCl long to ra Q ; cht hu c Q b oxi ha bi HNO3 long, nng thu c hn hp sn phm trong
c axit 2,3-imetoxibutanioic v axit 2,3-imetoxipropanoic.
Xc nh X, Y, Z, M, N
Cu 41: Xt phn ng th: RCl + OH ROH + Cl c biu thc tc phn ng l: v = k[RCl] hoc
v = k[RCl][OH ]
a.
Cho mt v d c th v RCl trong mi trng hp, gii thch
b.
S dung mi gii ca tert-Butyl bromua trong axit axetic xy ra theo c ch nh sau:
(CH 3 )3 CBr (CH3 )3 C+ + Br
(1)
(CH 3 )3 C + + CH 3COO (CH3 )3 COCOCH3 (2)
Hy gii thch ti sao, khi tng hm lng Natriaxetat th khng lm tng tc phn ng.
Cu 42: imetyl ha iso-butilen (X) trong dung dch H2SO4 60% thu c hp cht A mch h c cng
thc phn t l C8H16. Hiro ha A thu c B l 2,2,4-trimetylpentan. Nu dng Y l iso-butan tc dng
vi X cng thu c B khi c xc tc HF
a. Vit cc phng trnh phn ng xy ra
b. Trnh by c ch phn ng X A v Y B
c. Thnh phn % ca B trong xng gi l g? ng dng ca B trong xng?
Cu 43: Hp cht A c CTPT C4H8O3 quang hot, tan tt trong nc to dung dch c mi trng axit. Khi
b t nng A to ra cht B c CTPT C4H6O2 khng quang hot, t tan trong nc (dung dch c mi trng
axit). B phn ng vi KMnO4 d hn A. Khi b oxi ha bng dung dch axit cromic long th cht A bin
thnh cht lng C c CTPT l C3H6O. Bit C c nhit si thp, khng lm mt mu dung dch KMnO4
nhng phn ng vi I2 trong NaOH to ra kt ta mu vng.
Xc nh CTCT ca A, B, C v vit cc phng trnh phn ng xy ra.
Cu 44: Hp cht A (C18H18O2Br2) phn ng c vi dung dch NaOH nng. Cho hn hp sau phn ng
tc dng vi dung dch axit v c long thu c cht B (C9H9O2Br) v C ( C9H11OBr). Oxi ha B hoc C
u thu c axit p-Brombenzoic. Oxi ha C trong iu kin thch hp s chuyn thnh B. T B thc hin
d
c
dd NaOH(
H2 SO4(
Cl2 ,as
dd HCl
)
)
D
E
G
H
chuyn ha sau: B
to
170o C
Bit D cha mt nguyn t Clo trong phn t. Cc sn phm ghi trn s u l sn phm chnh
Vit CTCT ca A, B, C, D, E, F, G, H v vit cc phng trnh phn ng xy ra. G, H c ng phn hnh
hc khng. So snh nhit nng chy ca B v C. Gii thch
Cu 45: Khi cho amoniac phn ng cng vi axetanehit thu c sn phm khng bn A, sn phm ny
d b tch nc thnh B. B d dng trime ha cho sn phm C l triazin. Mt khc nu cho amoniac ngng
t vi fomanehit s thu c sn phm D (urotropin) c CTPT l C6H12N4. Cht D c kh nng tc dng
vi axit nitric trong anhirit axetic to ra E (hexogen hay xiclonit) l cht n mnh c dng trong i
chin th gii th II theo s : C6H12N4 + 3HNO3 E + 3HCHO + NH3.
Xc nh A, B, C, D, E v vit cc phng trnh phn ng xy ra.
Cu 46: Tch hn hp cc cht sau: hexan-2-on ; hexan-3-on ; axit fomic ; axit trietylaxetic
Cu 47: Vit cc phng trnh phn ng theo s sau:
+X
C (etilen glicol iaxetat)
o
H 2 ,xt
P,t ,xt
Trng
ngng
2HCHO A
D (poliete)
B
O2 ,xt
Ca (OH ) 2 ( d)
+ CuO, t
F (axit a chc)
E
G
o
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Cu 48: Khi cho PVC tc dng vi Zn trong ru th tch ra c ZnCl2 v thu c polime c cha
20,82% clo. Polime khng cha ni i v khng c tnh do nh PVC. Kt qu trn cho bit g v cu to
ca polime mi thu c. Tnh % mc xch vinyl clorua b tch clo bi Zn.
Cu 49: X l - halogen xeton vi baz mnh to thnh cc sn phm chuyn v. S chuyn v ny gi l
phn ng Favorski. - cloxiclohexanon s chuyn v thnh metylxiclopentancacboxilat khi c mt
CH3ONa trong ete. Hy xc nh c ch ca phn ng ny.
O
Cl
CH3ONa
ete
COOCH3
NaCl
C DFe / HCl
E F
1:1
HNO
(1 mol)
Cu 53: Hp cht hu c A c cng thc phn t dng CxHyOz trong oxi chim 29,0909% v khi
lng. Bit A c th phn ng vi dung dch NaOH vi t l 1:2, phn ng vi Br2 theo t l 1:3. Xc nh
cng thc phn t v cng thc cu to ca A.
Cu 54: So snh tnh baz ca cc cht sau v gii thch: CH3NH2, NH3, (CH3)2NH, C2H5NH2, C6H5NH2,
(C6H5)2NH, NaOH, C2H5ONa
Cu 55: Vit cng thc cu to ca cc cht hu c c tn gi sau:
a.
Spiro-[3,4]-oct-1-en
b.
(R)-3-clobut-1-en
Cu 56: Inden co cong thc phan t C9H8 co cac tnh chat sau:
- Lam nhat mau dung dch nc brom, dung dch nc thuoc tm.
- Hap thu nhanh 1 mol H2 tao thanh Indan (C9H10).
- Tac dung vi H2 d (xt Ni, t0) tao hp chat C9H16.
- B oxi hoa bi KMnO4/H2SO4 tao axit Phtalic
Xac nh Cong thc cau tao cua Inden. Viet cac phng trnh phan ng
xay ra.
Cu 57: So sanh kha nang phan ng the electrophin cua Naphtalen vi
Benzen. So sanh kha nang phan ng (co giai thch) the electrophin v tr
va v tr cua naphtalen. Viet cac phng trnh phan ng ieu che ra
cac dan xuat initronaphtalen va axit naphtalenisunfonic t naphtalen.
Cu 58: Oxi ho 150 mg amiloz bi NaIO4 thu c 0,0045 mmol axit fomic.
a. Tnh s lng trung bnh cc gc glucoz trong phn t amiloz; bit rng khi
oxi ho 1 mol amiloz bng NaIO4, s gc glucoz u mch to ra 1 mol axit
fomic, s gc glucoz cui mch to ra 2 mol axit fomic.
b. Vit s cc phng trnh phn ng xy ra.
Cu 59: T CH4, cc cht v c, xc tc v cc iu kin phn ng cn thit, vit s iu ch cc cht
hu c sau: PPM, PVA, DDT
3
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H
HO
H
HO
Br2
H2O
CaCO3
H2O2
HNO3
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Khi oxi hoa A th thu c mot hp chat d vong B co cong thc C5H4NCOOH.
Biet rang trong ca hai phan ng tren khong co s ong hay m vong
va phan t coniin khong co C bac ba.
a. Xac nh cong thc cau tao cua coniin va cho biet bac amin cua
coniin A, B . V sao khoi lng phan t cua coniin, cua A, B eu la so le.
b. e tach lay coniin t hat oc sam vi hieu suat va o tinh khiet
cao nen chiet vi dung moi nao sau ay (co giai thch) : Nc, ru
etylic, dung dch NaOH, dung dch HCl.
Cau 66: Hp chat A (C5H9OBr) khi tac dung vi Iod trong moi trng kiem
tao ket tua mau vang. A tac dung vi dung dch NaOH tao ra hai xeton B
va C co cung cong thc phan t la C5H8O. (B) va (C) eu khong lam
mat mau dung dch KMnO4 lanh, ch co B tao ket tua mau vang khi
tac dung vi Iod trong moi trng kiem. Cho B tac dung vi CH3MgBr roi
vi nc th thu c D (C6H12O). D tac dung vi HBr tao ra 2 ong phan cau
tao E va F co cong thc phan t C6H11Br trong o ch co E lam mat mau
dung dch KMnO4 lanh. Dung CTCT, viet s o phan ng t A tao thanh
B, C, D, E, F. Viet ten A va D theo danh phap IUPAC.
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