Based on the structure i.e depending upon the number of halogen atoms in a compound, Alkyl/ Aryl halides are classified as mono, di, and polyhalogen. When compared to carbon, halogen atoms are more electronegative. Therefore
- The bond (carbon-halogen bond) of alkyl halide is polarised.
- Halogen atom carries a partial negative charge
- Carbon atom carries a partial positive
Preparation Of Alkyl Halides
Alkyl halides are produced by the free radical halogenation of alkanes-
- Step 1 – Adding halogen acids to alkenes
- Step 2 – Replacing –OH group of alcohols by halogens with the use of phosphorus halides or halogen acids or thionyl chloride
Aryl halides are prepared with the help of electrophilic substitution to arenes. Iodides and Fluorides are prepared with halogen exchange method. Organohalogens have a higher boiling point when compared hydrocarbons due to strong van der Waals forces and dipole-dipole forces. They partial dissolve in water but completely dissolve in organic solvents.
Organometallic compounds are formed by the nucleophilic substitution, elimination, and reaction with metal atoms which occurs due to the polarity of a carbon-halogen bond of alkyl halides. Based on the kinetic properties Nucleophilic substitution reactions are classified as SN1 and SN2. Chirality plays a very important in SN2 reactions of understanding the reaction mechanisms of these reactions. SN2 reactions are characterized by inversion configuration whereas SN1 reactions are characterised by racemisation.
Few Important Questions
- Write the IUPAC names of ClCH2C≡CCH2Br
- Who has the highest dipole moment from the following?
CCl4 and CH2Cl2
- Write the steps to convert Propene to propan-1-ol and Benzyl alcohol to 2-phenylethanoic acid.
- Define ambident nucleophiles? Give an example and explain.
- When n-butyl chloride is treated with alcoholic KOH, what is the result?
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