What is Dehydration of alcohols
What is Dehydrohalogenation of Alkyl Halides
Nitration of benzene
Sulphonation of benzene
Halogenation of benzene
Iodination of benzen
It is carried out in the presence of HNO3, HIO3 to oxidise HI or it will be reversed
Friedel Craft Alkylation
Friedel Craft Acylation
Alkyl Halides to Alcohol
Reaction of Alcohols with Halogen Acids
Swart's Reaction
Finkelstein Reaction
Preparation of Alkyl Cyanides
Wurtz Reaction
Fitting Reaction
Wurtz-Fittig Reaction
Free Radical Substitution Reaction of Alkanes
Reaction of Chloroform with Air
What is Addition Reaction
They are characteristic reactions of unsaturated compounds
Alkene to Alkane
Preparation of Viccinal Dihalide
Diazotisation Reaction
Sandmeyer’s Reaction
Few Reactions of Diazonium Chloride
Balz Schiemann Reaction
Reduction of Nitrobenzene
Gattermann Reaction
Borodine Hunsdiecker Reaction
Silver Benzoate to Bromo Benzene
Acidic character of terminal Alkynes
Step up reaction of Sodium Alkanide
Alcohol to Alkyl Halide
Lucas Test
Iodoform test
Ethanol is the only primary alcohol to give a Positive Iodoform Test
Ethanal is the only Aldehyde to give positive
Iodoform Test
Test double bond in molecules
What are Ambident Nucleophiles
Groups possessing two nucleophilic centres
What are SN2 Reactions
In this reaction the incoming nucleophile interacts with the Alkyl Halide causing carbon-halide bond to break with new bond is being formed by the Nucleophile, the carbon attacked inverts while leaving group is pushed away causing Inversion of Configuration
It is Bimolecular,Single Step
It follows Second Order kinetics
Rate of this reaction depends on both reactant and nucleophile
Attack will be always from rear side
1°>2°>3°>benzylic
What are SN1 Reactions
First the carbon-halide bond undergoes slow cleavage to produce carbocation and a halogen ion. The carbocation formed is attacked by the Nucleophile.
It is aUnimolecular, Two step reaction
It follows First Order of Kinetics
The attack can be from any side
There is retention as well as inversion of Configuration
Benzyliz>1°>2°>3°
Preparation of Grignard’s Reagent (which is an organo-metallic compound)
Grignard's Reagent to hydrocarbons
Grignard's Reagent are highly reactive and react with any source of proton to give hydrocarbons
Why are Aryl Halides extremely less reactive towards Nucleophilic Substitution Reaction
1.Partiacl double bond between carbon and halogen due to resonance
2.The carbon attached to halogen is sp2 hyberdised unlike the carbon in haloalkane which is sp3, greater s-character makes it more electronegative holding electron pair of C-X bond more tightly
3.As the phenyl cation formed will not be stabalised by resonance,therefore SN1 is ruled out
4.It is less likely for a electron rich Nucleophile to approach electron rich arenes because of the repulsion
Haloarene to phenol
What increases the reactivity of Haloarenes
Presence of an electron withdrawing group(NO2) at ortho,para-positions
Why do electrophilic substitution reactions occur slowly in Haloarenes and require more drastic conditions campared to those of Benzene
Because of the -I effect of the halogen atom, it has some tendency to withdraw electrons from the benzene ring, somewhat deactivating it.
Dichloromethane
1.It is used as:
Paint remover
Propellant in aerosl
Process solvent in manufacture of drugs
Metal Cleaning
It harms human's nervous system
Exposure to low levels of it in air can slightly impaired hearing and vision
High levels of it in air causes dizziness, nausea, tingling and numbness in fingers
Direct skin contact causes intense burning and mild redness of the skin
Direct contact with eyes can burn the cornea
Trichloromethane
(Chloroform)
It is used as:
Solvent of fats,alkanoids,iodine and other substance
Production of the freon refrigerant R-22
Was used as anaesthetic
Inhaling it depresses central nervous system
Inhaling 900ppm of it for a short time causes dizziness, fatigue and headache
Chronic exposure of it may cause damage to liver, kidneys
Some people develop sores when their skin is immersed in it
Triiodomethane
(Iodoform)
Tetrachloroethane
(Carbon tetrachloride)
Freons
p,p’-Dichlorodiphenyltrichloroethane
(DDT)
Williamson’s synthesis
Alkyl/Aryl Halide to Alkane
Dow’s process
Zuletzt geändertvor einem Jahr