Chemistry > Hydrocarbons > 3.0 Methods of Preparation Alkanes
Hydrocarbons
1.0 Introduction
2.0 Alkanes
3.0 Methods of Preparation Alkanes
4.0 Physical Proparties
5.0 Chemical Properties
6.0 Alkenes
7.0 Methods of Preparation Alkenes
7.1 Dehydrohalgoenation
7.2 Dehydration of Alcohols
7.3 Dehalogenation
7.4 Thermal elimination reaction
7.5 By partial reduction of alkynes:
7.6 Wittig Reaction
7.7 Kolbe hydrocarbon synthesis
8.0 Physical Proparties
9.0 Chemical Properties
10.0 Mechanism Of Some Important Reaction Of Alkenes
10.1 Mechanism of halogen addition
10.2 Mechanism of halohydrin formation
10.3 Syn - hydroxylation
10.4 Oxidation reactions of alkenes
11.0 Alkynes
12.0 Methods of Preparation Alkynes
12.1 Industrial source
12.2 Kolbe’s method
12.3 Dehydrohalogenation of 1, 2 – dihalides
12.4 Dehydrohalogenation of 1, 1 – dihalides
12.5 Dehalogenation of tetrahalides or trihalides
12.6 Alkylation of acetylene and terminal alkynes
13.0 Physical Properties
14.0 Chemical Properteis
14.1 Electrophilic addition reactions
14.2 Acidity of Alkynes
14.3 Aromatic Hydrocarbons
14.4 Structure of Benzene
15.0 Modern Concept
15.1 Aromaticity in Benzene and Related Systems
15.2 Huckel’s rule or $\left( {{\bf{4n}}{\text{ }} + {\text{ }}{\bf{2}}} \right)\pi $ electron rule
16.0 Properteis
17.0 Mechanism of Electrophilic Substitution Reactions
17.1 Nitration
17.2 Friedel – Craft Alkylation
17.3 Friedel – Craft Acylation
17.4 Reactions of side chains
18.0 Toluene
19.0 Alkenyl Benzene
3.2 From Organometallic Compounds
7.2 Dehydration of Alcohols
7.3 Dehalogenation
7.4 Thermal elimination reaction
7.5 By partial reduction of alkynes:
7.6 Wittig Reaction
7.7 Kolbe hydrocarbon synthesis
10.2 Mechanism of halohydrin formation
10.3 Syn - hydroxylation
10.4 Oxidation reactions of alkenes
12.2 Kolbe’s method
12.3 Dehydrohalogenation of 1, 2 – dihalides
12.4 Dehydrohalogenation of 1, 1 – dihalides
12.5 Dehalogenation of tetrahalides or trihalides
12.6 Alkylation of acetylene and terminal alkynes
14.2 Acidity of Alkynes
14.3 Aromatic Hydrocarbons
14.4 Structure of Benzene
15.2 Huckel’s rule or $\left( {{\bf{4n}}{\text{ }} + {\text{ }}{\bf{2}}} \right)\pi $ electron rule
17.2 Friedel – Craft Alkylation
17.3 Friedel – Craft Acylation
17.4 Reactions of side chains
Grignard’s reagents and alkyl lithium reacts with water and other compounds having acidic hydrogen to give hydrocarbon corresponding to the alkyl group of the organometallic compounds.
Grignard’s reagents reacts with alkyl halides to give alkanes
(Alkanes with higher number of carbons atoms)
