Professional Documents
Culture Documents
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
W
AMINES
A
1 Nomen clafkse CH NH, melhanamine
CH3-NH- C N methylenclhananine
N, N-imehyl methanamine
NH NH2
Hniline Tolui' dine
NS NH2
NO NO NO Snttz O
ONH
HO
NO
OH NH2 NH2
OH
NO2 NH2 No. NH O 2
NHyHS
N0
NO
NO
N02 NH2
alk FtSOy oo
nd TH
CHo) (CHO
LAHu tT H2tN;-
4.R-CEN_ >RGH, NH,
TNa tp/Gtgo
5 R-X
RX
R,NH >RN RN
NHz (extess)
6 Gabriels Phtlalinmide nthS
(OD
koHRXX +Nt-R
Coo
phthalimide
D
Hoftmam
cthaodé-oE Selicl X
-0
e
D)0.Agaut RNO, R,N-OH&,-
POattdo)
P hS 0 2 N R Ph-502NR
PHinSbux Teor PP pt (R) e taRe
h Ht HT NK3 exeo
Ph-SoYe)
Bunzo Gulphony PP xxx denr ol
Ph-S0,-NHR (R NH) N-SoPh Ph
Chlonde R
Nt OH
PHET2 13,
Ph-o p-Hydroy 02pbeng nt Orange dye
NtHNH2 N N Ni
P-ammoa ze benZerne yellew dye
OH
oH Me me N Me
Me
SoNa methy orange
PAGENo
DATE: I201
NH2
NH2 NH2
HNO3 BY2 NH2Br
H
NO 47 / NH2 Br whe pP
5R ( NHPh mala)
NH--Ha
NH2 NH2
NHa HSOy
H2y
ermajps)
25C
NH2 NH2 To
get 0 prpduct
SOaH Uuphianil'e block pava by Se H,
aud then hy droy se
SogH
Ph- C-
YY
Ph-C - NH-H
CBenzoylaton O
IS
R-NH, + R-C R-NF-R+ H
Pvidine wwd which enaunned He G_foswaz.
Date
CoOH
NO IDS Page No.
NH Serin - H2OOH
Aroine mreenive CH
0 Guind - H
Sif aa yrosine OH
Alanine
petlo, kat ae qulabjamun
P G
ysfen - CH,-SH
-C
Ag enfna zanori hai 5Methionine
Valin Aginine a .
yine
-CC 10 nen tao.
Avginine NH
12 ty H-NH- NH,
Prolinc NH
COOH
C
Pheny Alanine
Hisfdine NH,=-H=00H-
Tro sin
CH
Aspare Add CooH NH
NH
Gufamina H
NHa
Date
CoOH
NO IDS Page No.
NH Serin - H2OOH
Aroine mreenive CH
0 Guind - H
Sif aa yrosine OH
Alanine
petlo, kat ae qulabjamun
P G
ysfen - CH,-SH
-C
Ag enfna zanori hai 5Methionine
Valin Aginine a .
yine
-CC 10 nen tao.
Avginine NH
12 ty H-NH- NH,
Prolinc NH
COOH
C
Pheny Alanine
Hisfdine NH,=-H=00H-
Tro sin
CH
Aspare Add CooH NH
NH
Gufamina H
NHa
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Page No.
Date:
ETRERS
Prep 0wiliamson nth RoT+ Rx + R-0-R'
Cenc
R-OH R-0-R (R-OH acts ao Eand Nu
H E) Alkene
Alkoxy eY. Dem Ha CoAC,oH R-OH
Na BH NaOH
R-oH H-0H 0-C-H,wibe
ata ched
Ph-0+ROS-DR_ Ph-0-R+o-5-oR
oH
Boae)
Eporuy cc D, A
Xpfi
mepbA
aofev =c
Date
AidAad leauage
a) Demo mese kC_pe S1 S
b Deepe S V SNS2 V
Me
CH
ApHE Me
Anly HE R-OH+T-R
SN -
O-0-
O-0-CH=CH r DH+0= CH-H
Me-C C H
RMgX
me H
me Me- H
me OH Me
O2
Oxd R-OR R-0 - R- 0 -OH
(eny tat R which hag Stable
+2
Remeue fe" cene H,So faee Tadicol en i a t leaot 1 H)
KT +Stârch (8ue lelour)
O
Claisen Rea H2- CH=H
palat ke legta hai) -CH2-(H = H2 OH
-MR
baa
palas CH-H =H,
elasSMAte
Date
Page
GOC
RCR H-RH D
NRa -SA,> -NH NO So,R Ar
fewG)
(ewg)-C00H Fru>BrI -o-Ph oh -OR -2-R>
SH SR> -o CECR> -h - H=CR,
Kesonante. e C c - d -
mubmen c a fype efonane Stability ) no. bera
net a) enm eNTalem
-ve
hybrid alu shuckne aut cu
8) Chogecl/uncha 1¢e
XXy Cem mbulien
e N atom a ulta naui hola !
3 dliuiont 6cutnplile e
NH3 H0 4,8ruderphile
phonyl Ct CH Date
Page
benzylic
C)
Dantirg
esonnce
6FreeAadilal
CH2
Stabiy O
7Carbanon Sp
Stabiuty a
eCH eme
Me me
Caroene : CH
215Ttt-
Sp10
mulrplia tSinglet Triple
H
gentrolOfabiuly
( paihing energy in sing)
futk
ending CF2
V
ca, >:CB22
V V
CT2Singét
Cf2 Ca C62 :CT2 mplut
obenZyne (dthqdrobenzene)
Arcnmalie in nalúre
Sp-SpDuerap
alASSMAte
Date
age.
atp alomrs
Aromaliaty Cyclc + Cergugaled 7 fonar
Hutkh
Hutkh rule
Ly (tnt2) TT e3. Promauc.
4n Te 5 anf Fhpalic
H
H
NH2
fypical
N
NN-H H-NAN-H
3-Amulene nem-Qwmalic
1o-Anulene (nonplonwr)
non Armalre
plana
nen-planay Cyclo9CIofefen Cy clooctatelrene
danien
14-Armnubne npn- 4 p l i c BuT dtholro JArulert
0pmalic
nennen-plarar
H
H
P
Rx RR
RR
AUKANE 5 Cad
N/Pa/Pt
+ M2
NatDE. Wur6
]
Q9: koH N2
hi
HXC" muth
ALKYL
el
HALIDES PO2/Pa5 /Sou
ALCOHOLS
Lenc. S y4
AlC:
frs HerIRo»R
HXa ct
OR
D (443K) Ether)
R
OMD go, ITHf
ar OR li) Na®Hy
SH Mo
kOH
ploot 2
T
t Ba-0
Gulk bo0 >AKENESk
[II
(Anf) Jmp8A
Na
Ri
Na - Na
tinNako+0
Alc Acelone
ainlin)8
Ti
(viote)
DR
gam)
--
ranjan_tatsam
]
S.
No Named Reaction Reagent Use Remark
hi
No rkn on deactivated ring or with Ph-NH2, NHR, NR2
1. Friedel Craft Alkylation RX + AlCl3 Alkyl group on benzene C+ rearrangement
Order - RF > RCl > RBr > RI
el
3. Clemmenson Reduction Zn-Hg conc HCl C=O to CH2 Can reduce NO2
4. Wolff Kishner Reduction NH2NH2 in KOH C=O to CH2 Cannot reduce NO2
D
(i) SH-CH2CH2-SH in BF3
5. Mozingo Reaction (ii) H2 Raney Ni
C=O to CH2 Useful when comp is both acid and base sensitive
6. Corey House Synthesis Gillman Reagent - R2CuLi R2CuLi + R'X -----> RR'
T
THF not DE
10.
H2 + P2 Catalyst
Na in DE
[II Syn addition of H2 across alkyne
RX to R-R
CH3CH2X gives mixt of CH2=CH2 + CH3CH3 +
CH3CH2CH2CH3
15. Bayer's Reagent Cold Alk KMnO4 Syn addition of OH across C=C Pink/ Purple colour gets decolourised
Ti
16. FinkelStein Reaction NaI + Acetone R-Cl/Br --------> R-I NaBr/Cl are insoluble in acetone
17. Swartz Rkn AgF/ SbF3/ CoF2/ Hg2F2 RX --------> R-F Aaj Sab ko hugg (Ag Sb Co Hg)
ranjan_tatsam
18. Darzen Procedure SOCl2 in pyridine ROH to RCl without rearrangement Inversion of configuration
19. Reimer Tieman Reaction NaOH + CHCl3 Phenol to Salicadehyde dichloro carbene is E+
]
20. Kolbe Schmidt Reaction NaOH +CO2 Phenol to Salicylicacid
hi
21. Williamson Synthesis of Ethers RL + RONa Ethers prep Elimination may take place
el
CrO2Cl2 Toulene to Ph-CHO
[O]
D
Applicable to phenol (and their etheres); Not applicable
Deactivated rings; Benzene with NH2/ NHR/ NR2
26. Gatterman Formylation Reaction Zn(CN)2 + HCl Benzene to Benzaldehyde
28. Stephen's Reduction (i) SnCl2 + HCl (ii) H2O RCN ---------> RCHO
T
Must have α H; Can dehydrate easily; LDA will pick
29. Aldol Condensation Dil NaOH Ald/Ketones -----> β hydroxy Ald/Ketones most acidic H (100% enolate formation no self aldol)
while NaOH will form stable enol
]
hi
Disproportionation rkn; there shouldn't be any α H. RDS
34. Cannizaro Reaction conc NaOH R-CHO -------> RCOO- + RCH2OH
is transfer of hydride ion.
el
Stereoselective - trans > cis
35. Wittig Rkn Ph3P=CH2 Regioselective - better than E2 (Double bond in just one
place)
D
36. Tischchenko Reaction Al(OR)3 RCHO -------> RCOOR
T
37. Knoevenagel Condensation
]
hi
Yield of RX : 1 > 2 > 3
42. Hunsdiecker Reaction Br2 + CCl4 + Heat If RCOOAg and I2 are taken as 2:1 then ester is formed
and in 1:1 R-I is formed (Simonini Reaction)
el
43. Hell Volhard Zelinsky reaction Red P + X2 + Heat
D
-------> R-N=C=O (Ketime)
Hoffman Bromamide Degradation
44. NaOH + Br2 N loses both its H
(Rearrangement) no Cross only self
Only 1degree amines
T
46. Curtius Rearrangement (Same as Hoffman, in place of Br- we have -N2+)
48. Sandmeyer
CuCl + HCl
CuBr + HBr
[II On Benzene Diazonium salt to get halo/cyano benzene
Only 1 degree amines
No Aromatic amines
CuCN
Cu + HCl
49. Gatterman
ru
Cu + HBr On Benzene Diazonium salt to get halobenzene
(i) HCN
51. Kiliani Fischer Synthesis (ii) H3O+
Ti
]
hi
el
D
T
[II
ru
Ti
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Ti
ru
[II
T
D
el
hi
]
Page No.
PHENOLS Date
EPREP
7 Y Me 1
683 71 Na0H
3oha HhSo enC HNO
H
So NO2 O1me
ummone
toouad
SnH
HO
DS1NaNo,t (mistien)
H wo H0 OH 0
OH OH
Keinne lienmann
Penai
6laum
eno
quineme
:CCe
C OH OH
OH
Sreom NO2
disflafion)
CenC
HNO
OH
(O-CooH
Page No.
Date
L o t )
C h - - o H
0-CH
HC00
DK
-Ch,
-CoEH
R
Pspimin
OH
CH CH OH
Ht
AG0-
pil winleigpe
PhOH
O
OH
+0,
C-010Salel
(ankdephe (saticqbe acid
Pheuol
N=0
HNO2
NU
CH-C-0
O So DH
HO -So
NO uNO
NO
NO
Page No.
Date
In kolbes kn
ONaT O
T1Y0'c
G80th paa
CwPT
ONa OH
P 4-6 an
OK OH
k,
Co
OH NH,
Zn
OH
cluor
C CHO
(aye)
Page No.
Date
TESTS
0 wolet Celour w lral ted
Erete Lonen
LNiheso (Libes mann)
OH
OH
NoNo
HCe
N
ONAO Indephenol
NaO
CkoHT
d u e 1 o e t e o b l
Azodye Teot
OH
HOON-N O
Paoahydrot Azo enzene
B , aq) s t e p
OH
67
POC
nmayy
trUAttFARUE- a (oH
CalDtHh0 G(Ho)
Mitkindd
C
Ba(o)a> baC H o BaBa CHo)
nilkiness
SAy
H Cuso,5 H,o
Bue
t2
+2
NetFeet
NaFe C), NoS Vinst
Na, S
Pb(OH,Coo0h PbS)
)black ppt
To emoue S/CN aH,S)HCN
HND, (Pn N,)
x Na x Ba lute ioluble
aBr Pols yeleud PaxialPelbblk_
yellou Tnieleb
fhmma phho nelajbcld
Duma M TELDAH
a) uo N21 a) nso NH2NH4 J A
b) N ka Vel guen
6 NH3
c) tfratien with 504 V
3X Caiu NO C o + Ho t
given
No
() HNO
6all Ba SOy
wt giun V
Louiuo Tube)
MNO HPo
Armm
molybdake
Ticase
Mg NHy PO 2 P0q
H ,Po2 Mo0
Giuen w.
6
COTp
+2
Co kei eR Ra
w iven
St0+1,05 I,+5O
POLYMERS
S. No. Name Monomer(s) Structure Remark/ Catalyst
]
hi
Persulphate Or Free Radical
1. Teflon as catalyst
el
3. Polyethene
LOW => O2 as catalyst
D
a) LDP High Temp (350-570K) and
pressure (1000-2000 atm)
T
atm)
PMMA
4.
(Polymethylmethacrylate)
[II
5. Nylon 5
ru
6. Nylon 6
Ti
7. Nylon 6,6
]
hi
8. Nylon 6,10
el
9. Nylon-2 Nylon-6
D
Zinc Acetate and Antimony
10. Dacron/ Terylene Trioxide
T
11. Glyptal
Phenol Formaldehyde
[II
12.
Resin
ru
a) Novolec
Ti
b) Bakelite
Malamine Formaldehyde
13.
Resin
]
hi
14. Urea Formalehyde Resin
el
Elastic Properties
Latex - Colloidal soln of rubber in
15. Isoprene (Natural Rubber) water
Coiled (Spring) structure
D
Vulcanised Rubber Heat raw rubber with S.
T
Neoprene (Synthetic
16.
Rubber) [II
Buna-N (Synthetic
17. Peroxide
Rubber)
ru
18. Buna-S
Ti