Most of you might feel difficulty while dealing with reagents. In this article of ours we have listed the Important Reagent Formulas in the form of tables for your understanding. Grasp the concept and start answering the questions at a faster pace. To assist you we have curated different formulaes on Kuchroves, Antihydrating, Oxidising, Reducing Reagents, etc. Get acquainted with the reagents that you need to know about with our Reagents Formulae List.
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A. IMPORTANT REAGENT:
1. dil H2SO4 [or Cone. H2SO4] + H2O]
Use → Hydrating agent (+HOH)
(c) Kuchroves reaction
2. aq. KOH or moist Ag2O or aq. AgOH
Use → [-X → -OH] or + OH
3. alc. KOH or NaNH2 [Use → -HX]
4. Isomerisation Reagents of hydrocarbons
For alkene → AlCl3 / HCl
For alkene → Al2(SO4)3
– ale KOH
For alkyne – (to form disubstituent alkyne)
– NaNH2 (to form terminal alkyne)
5. R-X
6. Zn dust Use → (a)(For – X2)
(b) For deoxygenation
7. HNO2 Use → (-NH2 → – OH)
Diff. reactions:
8. Cu or ZnO /300° C
9. CH2N2 Use → (for + -CH2 (group))
10. Soda Lime NaOH + CaO
Use – for decarboxylation (emits -COOH or-CO2)
B. IMPORTANT ANHYDRATING REAGENTS:
2. P2O5 Use
3. Anhy. ZnCl2 Use → In Grove
4. Al2O3 Alumina use: →
5. KHSO4
6. Dry HCl gas use →
7. Cone. H2SO4 use →
C. IMP. OXIDISING REAGENTS:
1. Alkaline KMnO4 (Strong oxidant)
Toluene → Benzoic acid
2. Acidic KMnO4 (Strong oxidant)
3. Bayer’s Regent
1% alkaline KMnO4 (Weak oxidant)
Use: → For test of > C = C < or – C ≡ C –
4. O3 Use → In determination of position of
> C = C < or – C ≡ C–
5. Acidic K2Cr2O7 (Strong oxidant)
6. CrO2Cl2
7. Br2 Water use: → For test of unsaturation
8. Alkaline H2O2 use →
(In brief Anti MR HOH on alkene or alkyne)
NOTE: Oxidation series
Alkane → Alc → Aid. or ketone →
Carboxylic acid → CO2
D. IMP. REDUCING REAGENTS:
1. SnCl2/HCl or Sn/HCl use → for redn of nitrobenzene in acidic medium.
2. Zn/NH4Cl or A1 – Hg/NH4Cl use →
for reduction of nitrobenzene in neutral medium
3. Red P/HI
RCOR or RCOOH or RCHO or ROH or
Note:
4. Zn – Cu / EtOH or Na – Hg (or Al – Hg)/EtOH
R – X + 2H → RH + HX
5. Zn – Hg / cone. HCl
6. LiAiH4 (Strong reductant)
7. Na/C2H5OH
E. IMP. CATALYST:
1. Diastase (1) Maltase (2) Zymase (3)
2. Invertase (1) Zymase (2)
3. Raney Ni ⇒ Ni powder + Rescent H or Ni – Al/NaOH
4. Lindlar’s Catalyst = Pd/CaCO3 + in small quantity (CH3COO)2Pb
5. BF3:
6. BF3.HgO:
7. BF3.H2O:
8. Hg+2 Use → In Kucherov’s reaction:
9. FeCl3 (Lewis Acid):
10. Anhy AlCl3 (Lewis Acid):
use: → In Friedel Craft reaction
11. Pd/BaSO4, Pd = Catalyst, :
BaSO4 = Cat. poision
12. (A) Cu2X2/HX → Sandmair reaction
(B) Cu powder/HX → Gattermann reaction
13. ThO2 (Thorieo):
14. SiO2 (Silica):
15. (C2H5O)3 Al, AlCl3 in Tischenko reaction.
16. Ziegler – Natta Catalyst (C2H5)3 Al + TiCl4
Use → In Addition polymerisation
17. Anhy. ZnCl2:
18. Co Use → In oxo of formylation of carboxylation reaction:
19. Ni
(a) In SS reaction:
20. (C6H5)3 P + Ni (CO)4:
21. dry ether:
(3) In Wurtz reaction
(4) In Wurtz Fitting reaction
22. Acetone:
Use: → In Finkelstein reaction
23. C2H5ONa:
Use: → (a) In Gurbet condensation
(b) In Claisen Ester condensation
24. ZnO + Cr2O3:
25. Pyridine:
Use → In Darzon process
26. Kisselghur process:
27. CHCl3 + ale. KOH → xxCCl2:
use:
(a) In Reimer Tiemannformylation
(b) In Hoffmann carbyl amine reaction.
28. Neutral FeCl3
PHYSICAL STATE OF COMPOUNDS:
g → gas, l → liquid, s → solid,
CH4 → g, C2H6 → g, CH2 = CH2 → g, CH ≡ CH → g,
CH3Cl → g, CH3BR → Poisonous g, CH3 I → l,
CH3CHCl2 → l, CH2Cl – CH2Cl → Sweet smell l,
CHCl3 → Sweet smell l, CHBr3 → l, CHI3 → pale yellow S,
CH3OH → l, C2H5OH → l, Et2O → l, HCHO → g,
CH3CHO → l, CH3COCH3 → l, CH3COOH → l,
HCOOH → l, CH3COCl → Volatile l,
CH3CONH2 → crystalline compound (S), (CH3CO)2O → l,
CH3COOC3H5 → l, CH3NH2 → g, C2H5NH2 → g,
Urea → Crystalline S, C6H5 → colourless l,
C6H5NH2 → Colourless l, C6H5OH → white crystalline S,
C6H5NO2 → Pale yellow oily l, C6H5CHO → l,
C6H5COOH → white crystalline S.
MAIN USE OF COMPOUNDS :
Alkane → fuel, Alkene → polymer,
Alkyne → Solvents making like westron, Westrosol,
General alkyl halide → as solvents, CHCl3 → Anaesthetic,
Germicide, CH3 → Antiseptic & deodorant,
CCl4 → Pyrene & Fire distinguser, CH3OH → Antifreeze,
Deforming of alcohol, C2H5OH → Tonic, wine preparation
Power alcohol, C2H5-O-C2H5 → Anesthetic,
Natellite, HCHO → Formamint medicine,
CH3CHO → Antiseptic, CH3COCH3 → as solvent,
CH3COOH → Vinegar, HCOOH → (Coagulation of Latex)
CH3COCl → Acetylant, (CH3CO)2O → Acctylant,
Celulose acetate, CH3CONH2 → for C ↓
CH3COOC2H5 → Artificial silk & flavour,
CH3NH2 → Refrigerating agent,
C2H5NH2 → in development of photography, Urea → Fertilizing,
C6H5Cl6 → Germicide & Gamaxen,
C6H5NH2 → Preparation of dyes, C6H5OH → HPh,
Picric acid C6H5NO2 → In FCR use as a solvent,
C6H5CHO → Preparation of dyes,
C6H5COOH → Na-salt preservation of food.
SMELL OF SOME COMPOUNDS :
CH3COOC2H5 → Fruity, CHCl3, CH3I, C2H5I → Sweet smell
C6H5NO2 & C6H5CHO → Like bitter almonds
CH3COOH → Like vinegar, HCHO, CH3CHO,
CH3COCl → Pungent
CH3NH2 & C2H5NH2 → Fishy,
Impure CH3CONH2 → mice like, ROH → wine
RNCS → Mustard oil, methyl salicylate → wintergreen oil,
RNC → Fowl smell
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