Alkyl halides

Cards (64)

  • Methanol (CH3OH) has one carbon atom, while ethanol (C2H5OH) has two carbon atoms.
  • Geometry of methyl chloride is Tetrahedral with bond angle 109°
  • Formula of Thionyl halide is SOX2.
  • Reactivity order of halogen acid is HI>HBr>HCl
  • Alkyl halide is prepared by reacting alcohol with Hydrogen chloride anhydrous zinc chloride is used as a catalyst
  • Alkyl halide is prepared by reacting alcohol with thionyl chloride in the presence of Pyridine as a catalyst.
  • Typical reagent for OH is NaOH and KOH
  • Typical reagent for SH is KSH
  • Typical reagent of CN is NaCN
  • Typical reagent of CH3-COO is CH3-COONa
  • Typical reagent of CH3-CH2-O is CH3-CH2-ONa
  • Typical reagent of NaNH2 is NaNH2
  • Thiol is also called Mercaptan
  • R-COOR is the formula of Ester
  • R-O-R is the formula of Ether
  • R-NH2 is the formula of Primary amine
  • SN1 mechanism is a bi-step reaction
  • SN1 is unimolecular reaction
  • SN1 involves the formation of Carbocation intermediate in the 1st step
  • SN1 mechanism is carried in tertiary alkyl halides
  • Ordet of reaction for SN1 reaction is 1st
  • Rate of reaction on SN1 depends only on the conc. of substrate
  • In SN1, first step is the slow and rate determining step.
  • In SN1, the second step is fast.
  • SN2 mechanism is bimolecular single step reaction.
  • SN2 mechanism is carried in primary alkyl halides and methyl halides
  • Order of reaction for SN2 is 2nd
  • Rate of reaction of SN2 mechanism depends upon conc. of both substrate and attacking nucleophile
  • Nucleophilic Substitution Reactions takes place in aqueous medium while Elimination reaction takes place in alcoholic medium.
  • Nucleophilic Substitution Reaction is favoured by polar medium while elimination reaction is favoured by non polar medium
  • E1 reaction is unimolecular and bi-step.
  • E2 is bimolecular and single step reaction
  • In the first step of E1, halogen atom departs forming carbocation intermediate which is slow and rate determining step
  • In the 2nd step of E1, base abstraxt halogen atom from the carbon next to halogenated carbon and as a result double bond between both carbon is formed
  • In E1, rate of reaction depends only on the concentration of reactants not on the conc. of base
  • In E2 rate of reaction depends upon the conc. of both substrate and attacking base
  • Organic compounds that contain at least one halogen atom bonded to an alkyl group are called haloalkanes.
  • Monohaloalkanes are usually called alkylhalides represented by R-X
  • General formula of monohaloalkanes is CnH2n+1X
  • 1-bromopropane is a primary alkyl halide