Assalam o Alaikum
in this lecture i am going to discuss complete overview of oxidation and reduction with different types of oxidizing and reducing agents.i define oxidation and reduction in different angles.in oxidation types of Alcohol are discussed that are primary alcohol secondary alcohol tertiary alcohol.i oxidized all three types of alcohols and aldehyde ketone and carboxylic acid are formed.This lecture is delivered in Urdu ,Hindi and English.
oxidizing agents that are discussed in this lecture are following:-
1) Cr3 + H2SO4
2) Na2Cr2O7 + H2SO4
3) Na2Cr2O7 + H2SO4
These three oxidizing agents are the source of H2CrO4 OR Chromic acid.that oxidize alcohol to aldehyde and ketone and aldehyde and ketone to carboxylic acid.
4) PCC (Pyridinium chloro chromate )
this oxidize alcohol to aldehyde and ketone and reaction stop.it covert primary alcohol to aldehyde and secondary alcohol to ketone.
5) Baeyer Villiger reaction
in this per acid is used as oxidizing agent that oxide aldehyde to carboxylic acid and oxide ketone to ester.
6) MILD ACTIVE CATALYSTS OR oxidizing agent .
FEHLING SOLUTION :-
It oxide aldehyde to carboxylic acid ketones not give this reaction.
tollen solution OR oxidizing agent
It oxide aldehyde to carboxylic acid ketones not give this reaction.
Benedict solution or oxidizing agent
It oxide aldehyde to carboxylic acid ketones not give this reaction.
7) Alkenes can also be oxidized to epoxide by peracid or Baeyer Villiger reaction
8) hydroxylation of alkenes:-
in this we use these methods that are following:-
KMNO4 + OH
OSO4 + NAIO4
HFO4 + NAIO4
These oxidizing agents oxidize alkene to vicinal diol.and secondary alcohol to ketone.
9) ozonolysis :-
in this use O3 -78c and oxidative and reductive work up and obtain aldehyde ketone and carboxylic acid.
oxidative work up :-
dilute acid H3O+ + H2O
In this one product is aldehyde or ketone and second is carboxylic acid
reductive work up :-
Zn + CH3COOH
ZN/H2O
Pd/H2
(CH3)2
IN reductive work up Both products are ketones
Reducing agents :-
10) Hydrogenation in alkenes (catalytic reduction)
alkenes can be converted into alkanes by H2/Pt/Pd/Ni/H2 + Raney nikal
11) Rosenmund reduction:-
acylchloride can be converted OR REDUCE into ALDEHYDE by H2/Pd/BaSO4 AND R3N
or ALDEHYDE can be converted into primary alcohol.
12) Dissolving metal reduction:-
in this we use two types of reducing agents .one reduce alkyne or acetylene cis alkene that is H2/Pd/BaSO4. IN SECOND WE can reduce alkyne or acetylene trans alkene by K/Na in liquid ammonia. by hydrogenation we can convert it in normal alkanes.
13) Reduction with hydride:-
NaBH4 LiAlH4 BH3 DIBALH these are source of hydride.
NaBH4 REDUCE ALDEHYDE to primary & ketones to secondary alcohol .it does not reduce amides ester and carboxylic acid
LiAlH4
it reduce carboxylic acid to ALDEHYDE and ALDEHYDE to primary alcohol .it does reduce amides ester and carboxylic acid also.
DIBALH
reduce ester to aldehyde and primary alcohol.
i cover the following contents :-
1) oxidizing agents and reducing agents
2) oxidizing agents organic chemistry
3) oxidizing agents examples
4) oxidizing agents used in organic chemistry
5) strong oxidizing agents
6) chromium based oxidizing agents
7) best oxidizing agents
8) oxidizing and reducing agents class 10
9) oxidizing and reducing agents organic chemistry
10) oxidizing and reducing agents class 11
11) oxidizing and reducing agents class 9
12) oxidizing and reducing agents examples
13) good oxidizing agents
14) oxidizing and reducing agents in hindi
15) oxidizing agents in organic chemistry
16) mild oxidizing agents
17) reducing and oxidizing agents organic chemistry
18) oxidizing and reducing agents
19) oxidizing and reducing agents trick
20) oxidation and reduction in chemistry
21) oxidation and reduction kya hai
22) nabh4 reaction
23) nabh4 reduction
24) nabh4 mechanism
25) nabh4 vs lialh4
26) nabh4 reagent
27) nabh4 reaction with ketone
28) nabh4 and ch3oh
29) nabh4 aldehyde
30) nabh4 and ketone
31) nabh4 and ester
32) is nabh4 a nucleophile
33) is nabh4 a strong reducing agent
34) is nabh4 a reducing agent
35) is nabh4 a strong base
36) is nabh4 a lewis acid
37) nabh4 base
38) nabh4 benzaldehyde
39) nabh4 carboxylic acid
40) nabh4 carbonyl
41) nabh4 can reduce
42) nabh4 does not reduce
43) nabh4 to aldehyde
44) use nabh4 vs lialh4
45) nabh4 workup
46) nabh4 is used in organic chemistry to convert
47) why use nabh4 instead of lialh4
48) nabh4 vs dibal
49) bh3 as a reducing agent
50) bh3 vs nabh4
51) is bh3 a reducing agent
52) other oxidizing agent to replace potassium permanganate
53) 3 major oxidizing agents
#oxidation #reduction #pcc #baeyervilligerreaction #NaBH4 #LiAlH4 #BH3 #DIBALH #Lindlercatalyst #Rosenmundreduction #ozonolysis #Pd/BaSO4 #AuthenticEducationChannel
Assalam o Alaikum in this lecture i am going to discuss the reaction mechanism of the Jones Reagent which is used to oxidized primary alcohols into carboxylic acids and secondary alcohols into ketones. The jones reagent is composed of Chromium Trioxide CrO3, H2O, and H2SO4 (Sulfuric acid) which generates chromic acid H2CrO4. Oxidation of primary alcohols first generates an aldehyde which converts to the geminal / gem diol hydrate form which is then oxidized into a carboxylic acid. Tertiary alcohols are resistant to oxidation.This lecture is delivered in Urdu ,Hindi and English. 1° Alcohols are oxidized to carboxylic acids (RCOOH) under harsher reaction conditions: Na2Cr2O7, K2Cr2O7, or CrO3 in the presence of H2O and H2SO4. The mechanism for the oxidation of 1° alcohols to aldehydes parallels the oxidation of 2° alcohols to ketones detailed is discussed in this lecture. Oxidation of a 1o alcohol to a carboxylic acid requires three operations: oxidation first to the aldehyde, reac
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