NEET Organic Chemistry Hydrocarbons Videos

#1 - Methods of Preparation: Alkanes
(Organic Chemistry) > Hydrocarbons

21m 18shinglish

Wurtz reaction (02:10)

Sabatier-Senderens Reduction (10:41)

Decarboxylation reaction (12:14)

Kolbe's electrolytic method (14:20)

Preparation of methane (19:44)

#2 - Physical & Chemical Properies (Alkanes): Part 1
(Organic Chemistry) > Hydrocarbons

13m 07shinglish

Physical properties (00:01)

Halogenation(free radical substitution reaction) (07:24)

Nitration of alkane (07:57)

#3 - Chemical Properties (Alkanes): Part 2
(Organic Chemistry) > Hydrocarbons

12m 09shinglish

Sulphonation of alkane (00:01)

Isomerization (06:10)

Aromatization (09:31)

#4 - Chemical Properties (Alkanes): Part 3
(Organic Chemistry) > Hydrocarbons

13m 27shinglish

Pyrolysis (00:04)

Combustion reaction (05:20)

#5 - Methods of Preparation: Alkenes
(Organic Chemistry) > Hydrocarbons

04m 51shinglish

Preparation of alkene (00:37)

Kolbe's electrolysis (01:30)

#6 - Chemical Properties (Alkenes): Part 1
(Organic Chemistry) > Hydrocarbons

07m 15shinglish

Addition of water (01:35)

#7 - Chemical Properties (Alkenes): Part 2
(Organic Chemistry) > Hydrocarbons

hinglish

Addition of ozone(ozonolysis) (00:01)

Questions on ozonolysis (07:04)

#8 - Chemical Properties (Alkenes): Part 3
(Organic Chemistry) > Hydrocarbons

hinglish

Oxidation reaction (00:02)

Addition of chlorine (09:13)

NBS reagent (12:57)

#9 - Methods of Preparation: Acetylene
(Organic Chemistry) > Hydrocarbons

11m 34shinglish

From calcium carbide (00:41)

From chloroform and iodoform (01:15)

By dehalogenation of tetrahalide (02:24)

By dehydrohalogenation of vic or gem dihalide (03:24)

Kolbe's electrolytic method (08:05)

#10 - Chemical Properties: Acetylene
(Organic Chemistry) > Hydrocarbons

34m 13shinglish

Addition of hydrogen (00:19)

Lindlar's catalyst (01:55)

Addition of chlorine (04:11)

Addition of water (07:21)

Addition of Arsenic trichloride (11:06)

Cyclic polymerization of alkyne (14:11)

Reaction with Na (18:42)

Birch reduction (23:53)

Reaction with tollens reagent (25:35)

Reaction with ammoniacal cuprous chloride (29:09)