ORGANIC REAGENTS
S.No. | Reagent Function
1 PCh, PBrs, Pls Alcohols into Alkyl halides
2 [SoCh, PCls Alcohols into Alkyl chlorides &
_ Carboxylic acids into Acid Chlorides
3 | AC/ZnC, HBr. AI Alcohols into alkyl halides
4 | Ch/Fe or FeCl Cl group substituting on Benzene
S___ | NaNO; /HCI_0-5°C Diazotisation
6 | CuCl,CuBr,CuCN,KI,H20, | Diazonium Cholride into Chlor Benzene,
HPO; Bromo Benzene, Benzo nitrile, lodo
Benzene , Phenol,Benzene respectivel,
7___ | HBF, or NaBFy Diazonium Chloride into Floro Benzene
8 Agr or HgxF) or SbF; or _ | Alkyl halides into alkyl florides
k ‘OF 2
9 Na/ dry ether Alkyl halides into alkanes _
10 | NaOH 623/4437368K. Chloro benzene to phenol
| Br /FeBr3 Bromination of Benzene
12 | Chy/FeCly Chlorination of Benzene
13 | CH;CI/AICIs alkylation of benzene and its derivatives
14 [CH-CO-CI/AICh ‘Acylation on benzene
15 [H,SO,/HNO; ‘| Nitration of benzene
16 | (CHCO),0 /AICI, Q * Acylation of Ph
17 | H,SO4 Sulphonation on Benzene
18 | H,0/ HO, alkenes into alcohols
‘Aq KOH Alkyl halide into alcohol
19 | BH3/H202/0H" Alkenes into alcohols (Anti
Markownikoff product)
20 |NaBH,/LiAIH,(LAH) __| Aldehydes, ketones, acids into alcohols,
a Nito & Cynides , Isocyanides into amines |
21 or H,/Pd reduction of aldehydes, ketones and
cynides
22__| RMgXx/H,0" Aldehydes, ketones into alcohls
23 | O/H" ‘Cumene to phenol
24 ~|Na Alcohol or phenol into Sodium
alkoxide/Phenoxide
"25 |(CHCO),0/CH-CO-CI__| 0 acylation on phenol or N acylation on
Aneline or amine
[26 | Cone.HS0/443K Conversion of primary alcohols into
pe ee | alles = |
27__| Cone.H2S0,/410K Conversion of alcohols into Ethers
28 | 85% HPOs/ 440K Secondary alcohol into alkene
29 | 20% HsPOs/358K Tertiary alcohol into alkene
Alcoholic KOH
Alkyl! halide into alkeneORGANIC REAGENTS
30 | CrO/KMnO, or KzCr,07 | oxidation of alcohols into acids
in acidic medium
31 | CuS73k dehydrogenation of alcohols gives 1”
alcohols into aldehydes and 2” alcohols
into ketones & 3° alcohos into alkenes
32___ | Dil. HNO; Mono nitration of Phenol
33__ | Conc.HNOs tri nitration of phenol
34 | Bry/H;0 tri bromination of phenol
35__ | Bry/Csy mono bromination of phenol
36 | NaOH /CO2 Phenol to salicilic acid
37__ | CHCI,/NaOH Phenol to salcilaldehyde
[38 [Zndut [Phenol to Benzene z=
39 | NaxCr,0;/H,SOs or air | Phenol to Benzo quinone
40 | Zn/Cr03 200t0 300 atm | CO & H into methanol
573 ~ 673K.
41__ [invertase Sucrose into Glucose or Fructose
42___ | Zymase Glucose or Fructose into ethanol
43 [HI Ether into alcohol & alkyl halide
44__|PCC alcohol to aldehyde
45__| Pd /BaSO,.H2 [acid chloride into aldehyde
46 | SnCl,/HCV/H;0° Cyanides into aldehydes _
47__ | AIH(-Bu))/H,0 Cyanides into aldehydes
48_| DIBAL-H/H:0 Esters into aldehydes
49 | CrO2Cl:/H20 Toluene to aldehyde
50__ | CrO;/(CH3CO);0 Toluene into Benzaldchyde
St | Ch/hv Chlorination on alkyl group of Benzene or
he
52__ | CO, HCl anhydrous AICI;_| Benzene to Benzaldchyde
53__|(CH3)2Cd acid chloride into ketones
54 __| RMgX/H,0™ Cyanides into ketones
55__|HCN Carbonyl compound into cyanohydrin
56 | NaHSOs addition to aldchyde and ketone
57__ | H3NOH carbonyl compound into oxime
carbonyl compound into hydrazone _
carbonyl compound into Phenyl
hydrazone
carbonyl compound into 2,4 dinitro
phynyl hydrazone
61___ | H2N-NH-CO-CHs carbonyl compound into semi carbazide
62 [| ROH/HCI Aldehydes & ketones into hemiacetal and
acetal
63 | HO-CH,-CH2-OH/HCI__| Aldehyde or ketone into ethelene glycolORGANIC REAGENTS
ketone
64 | Zn-Hg/HCl carbonyl compound into alkane
65 | H:N-NH/KOH | carbonyl compound into alkane
66 | KMnO/OH7 K3Cr,0; Ketones into mixture of carboxylic acids
/HySO, or HNO3 on prolonged oxidation
67_|(Ag(NH)),)NOs+NaOH | Tollen’s test
68 | Cu(OH); Fehiling’s test
69 [NaOH+h Todoform
70 | NaOH or Ba(OH): aldal condensation
71___| Conc KOH or NaOH Cannizaro’s reaction
[72 | KMnO, /KOH Toluene/alkyl Benzene into Benzoic Acid
73 | HO" Cyanides into carboxylic acids, amides
into carboxylic acids, esters into
carboxylic acis and alcohols, acid
chlorides or anhydrides into carboxylic
acids
74 |NaOH Saponificaiton of ester, acid into salt of
acid
(75 ['NasCO; or NaHCO; Carboxylic acid test
(76 POio or P20s Dehydration of acids into anhydride,
amides into nitriles
[77__|ROH/concH,SO; ___| Caroxylic acids into esters
78 | PCI, SoCh, PCls ‘boxylic acids into acid chlorides
CHCO):0
(79 | NH; heating boxylic acids into amides
[80 | NaOH/CaO A xylation (acids into alkanes)
jst | LiAlHy xylic acids into alcohols, amides
into amines
82__[Chied Ps HVZ reaction
83 _ | Sn/HCl or Fe /HCI, Hi/Pd | Reduction of nitro compounds into
amines
84_[ NH; Alkyl halides into amines = |
85__| H2/ Ni or H2/Pd LiAIHy __| Amides into cyanindes
86__| KOH/R-X Phthalamide into amine
87__| NaOH /Brz Hoffman bromamide, amide into amine
with one :C “less
88 | KOH,CHCh ‘Amines into Carbyl amines
[89 | NaNO,/HCI 1” aliphatic amines into alcohols
[90 |NaNOJHCI_075°C___| Aniline into diavonium chloride
[91 | CuHsSO.Cl Distinguishing 1°,2° & 3° amines
92 | Bry/H30 Aneline into tri bromo aniline
93 | Bry/ CH-CO-CI Aniline into Bromo Aniline