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All Name Reactions Class 12 Chem

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54 views10 pages

All Name Reactions Class 12 Chem

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mohd.imaad.ahmad
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NAME

REACTION

JEETENDRonEEEEEEA

k ARYA
7077 6066 22
•
NDEX
• Aldol Condensation —————————————————— (21)
• Balz-Schiemann Reaction -——————————————— (03)
• Cannizzaro Reaction ——————————————————(23)
• Carbylamine Reaction ————————————————— (28)
• Clemmensen Reduction ————————————————(17)
• Coupling Reactions ——————————————————(29)
• Cross aldol condensation -———————————————(22)
• Etard Reaction -————————————————————(15)
• Fehling’s Test —————————————————————(20)
• Finkelstein Reaction ——————————————————(04)
• Fittig Reaction -————————————————————(08)
• Friedel-Craft’s acylation Reaction ————————————(10)
• Friedel-Craft’s alkylation Reaction ————————————(09)
• Gabriel phthalimide synthesis —————————————(27)
• Gattermann Reaction —————————————————-(02)
• Gatterman–Koch reaction ———————————————-(16)
• Hell-Volhard-Zelinsky ( HVZ ) Reaction ————————— (25)
• Hinsberg’s Test ————————————————————(31)
• Hoffmann bromamide degradation Reaction ———————(26)
• Kolbe Electrolysis ———————————————————(24)
• Kolbe’s Reaction ———————————————————-(12)
• Reimer-Tiemann Reaction ———————————————-(11)
• Rosenmund Reduction ———————————————— -(13)
• Sandmeyer Reaction ——————————————————(01)
• Stephen Reaction ———————————————————(14)
• Swarts Reaction ————————————————————(05)
• Tollens’ Test ——————————————————————(19)
• Williamson Synthesis —————————————————(30)
• Wolff Kishner Reduction ————————————————(18)
• Wurtz-Fittig Reaction ——————————————————(07)
• Wurtz Reaction ————————————————————-(06)
1. Sandmeyer Reaction:
The Sandmeyer reaction is a chemical reaction which is used to synthesize aryl
halides from aryl diazonium salts. This reaction is a method for substitution of an
aromatic amino group by preparing diazonium salt that is followed by its displacement
and copper salts often catalyze it.

2. Gattermann Reaction:
Bromine and Chlorine can be present in the benzene ring by preparing the benzene
diazonium salt solution with similar halogen acid present with copper powder. This is
called Gattermann Reaction.

3. Balz-Schiemann Reaction:
When arene-diazonium chloride is reacted with fluoroboric acid, arene diazonium
fluoroborate is precipitated. It is quite stable and is isolated. when heated to dryness,
it loses boron trifluoride and nitrogen gas and aryl fluoride is formed.

4. Finkelstein Reaction:
In the Finkelstein Reaction Alkyl iodides are prepared easily by the reaction of alkyl
chlorides with Nal in dry acetone.

5. Swarts Reaction:
When alkyl chloride is heated in the presence of a metallic fluoride like AgF, Hg 2F2 ,
SbF3 or CoF2, we get alkyl fluorides.

6. Wurtz Reaction:
When Alkyl halides get reacted with sodium with dry ether, we get hydrocarbons that
include the double number of carbon atoms present in the halide. This is known as
the Wurtz Reaction
7. Wurtz-Fittig Reaction:
When a mixture of alkyl halide and aryl halide gets treated with sodium in dry ether,
we get an alkyl arene.

8. Fittig Reaction:
Aryl halides prepared with sodium in dry ether to give analogous compounds where
two aryl groups joined.

9. Friedel-Crafts alkylation Reaction:


Benzene is reacted with an alkyl halide in the presence of anhydrous aluminum
chloride to give Alkylbenzene.

10. Friedel-Crafts acylation reaction:


We get acyl benzene when an acyl halide is reacted with benzene in the presence of
Lewis acid.

11. Reimer-Tiemann Reaction:


When phenol is reacting with chloroform in the presence of sodium hydroxide, —CHO
group is present at the ortho position of the benzene ring which results into
salicylaldehyde.
12. Kolbe’s Reaction:
Phenol reacts with sodium hydroxide to give sodium phenoxide which then reacts with
carbon dioxide in acidic medium to give hydroxybenzoic acid.

13. Rosenmund Reduction:


When Acyl chloride / Alkanoyl chloride is hydrogenated to give corresponding aldehyde
over a catalyst, known as Rosenmund catalyst which is H2 + palladium + barium sulfate.

14. Stephen reaction:


Nitriles with stannous chloride in the presence of hydrochloric acid are reduced to
the corresponding imine and give the corresponding aldehyde after hydrolysis.

15. Etard reaction:


Chromyl chloride oxidizes methyl group on benzene to get chromium complex which
on hydrolysis provides corresponding benzaldehyde.

16. Gatterman – Koch reaction:


Benzene is reacted with carbon monoxide and hydrogen chloride in the presence of
anhydrous aluminum chloride to give benzaldehyde.

17. Clemmensen Reduction:


In Clemmensen reduction, Carbonyl group of aldehydes and ketones on treatment
with zinc-amalgam and concentrated hydrochloric acid are reduced to CH2 group.
18. Wolff Kishner Reduction:
Carbonyl group of aldehydes and ketones on treatment with hydrazine which on
heating with sodium hydroxide in a high boiling solvent (ethylene glycol) reduced to
CH2 group.

19. Tollens’ test:


Heating an aldehyde with freshly prepared ammoniacal silver nitrate solution
produces a bright silver mirror deposition due to the formation of silver metal.

20. Fehling’s test:


Fehling’s solution A (aqueous copper sulfate) and Fehling solution B (alkaline sodium
potassium tartrate) are mixed in equal amounts before the test. A reddish brown
precipitate is obtained when an aldehyde is heated with Fehling’s reagent.

21. Aldol condensation:


Aldol and Ketol lose water to provide α,β-unsaturated carbonyl compounds which
are aldol condensation products. Carbonyl compound should have atleast one α-H .

22. Cross aldol condensation:


Aldol condensation is carried out between two different aldehydes and ketones. It
gives a mixture of four products if both of them includes α-hydrogen atoms.

MENTOR :- JEETENDRA K ARYA MOB:- 7077 6066 22


23. Cannizzaro reaction:
Aldehydes without α-hydrogen atom undergo self-oxidation and reduction reaction
when reacted with concentrated alkali.

24. Kolbe electrolysis:


In Kolbe electrolysis, An aqueous solution of sodium or potassium salt of a
carboxylic acid gives alkane containing an even number of carbon atoms on
electrolysis.

25. Hell-Volhard-Zelinsky ( HVZ ) reaction:


Carboxylic acids having a α-hydrogen are halogenated at the α-position give α-halo
carboxylic acids on treatment with chlorine or bromine in the presence of small
amount of red phosphorus.

26. Hoffmann bromamide degradation reaction:


An amide with bromine in an aqueous solution of sodium hydroxide produces
primary amines.
27. Gabriel phthalimide synthesis:
Phthalimide reacted with ethanolic potassium hydroxide to produce potassium salt of
phthalimide when heated with alkyl halide followed by alkaline hydrolysis forms the
corresponding primary amine.

28. Carbylamine reaction:


Aliphatic and aromatic primary amines when heated with chloroform and ethanolic
potassium hydroxide produces isocyanides or carbyl amines which are foul smelling
substances.

29. Coupling Reactions:


Benzene diazonium chloride gets reacted with phenol in which the phenol molecule
at its para position is mixed with the diazonium salt to give p-hydroxyazobenzene.

30. Williamson Synthesis :


An alkyl halide is allowed to react with sodium alkoxide. Ethers containing
substituted alkyl groups (secondary or tertiary) may also be prepared by this
method. The reaction involves SN 2 attack of an alkoxide ion on primary alkyl halide.
31. Hinsberg’s Test:
Benzenesulfonyl chloride (C6H5SO2Cl) reacts with primary and secondary amines to
produce sulphonamides.
1. The reaction of benzene-sulfonyl chloride with primary amine yields N-ethyl
benzene-sulfonyl amide. The hydrogen attached to the nitrogen in
sulphonamide is strongly acidic due to the presence of strong electron
withdrawing sulfonyl group. Hence, it is soluble in alkali.

2. In the reaction with a secondary amine, N,N-diethyl- benzenesulfonamide is


formed. Since N,N- diethyl benzene sulphonamide does not contain any
hydrogen atom attached to a nitrogen atom, it is not acidic and hence insoluble
in alkali.

3. Tertiary amines do not react with benzene-sulfonyl chloride.

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