🥼Organic Chemistry Unit 10 – Organohalides

What Are Organohalides?

• Organohalides are organic compounds that contain a carbon-halogen bond (C-X) where X is a halogen atom (fluorine, chlorine, bromine, or iodine)
• Consist of a hydrocarbon backbone with one or more hydrogen atoms replaced by a halogen atom
• Can be classified based on the type of halogen atom present (organofluorides, organochlorides, organobromides, or organoiodides)
• Play a crucial role in organic synthesis as versatile intermediates for the preparation of various functional groups
• Exhibit unique physical and chemical properties due to the presence of the electronegative halogen atom
  • Affects the polarity, reactivity, and stability of the molecule
• Found in various natural and synthetic compounds with diverse applications (pharmaceuticals, pesticides, polymers)
• Nomenclature follows IUPAC rules with the halogen treated as a substituent on the parent hydrocarbon chain

Structure and Nomenclature

• Organohalides have a tetrahedron geometry around the carbon atom bonded to the halogen with bond angles of approximately 109.5°
• The carbon-halogen bond is polar due to the difference in electronegativity between carbon and the halogen atom
  • Polarity increases in the order: C-I < C-Br < C-Cl < C-F
• Halogen atoms are named as fluoro-, chloro-, bromo-, or iodo- depending on the specific halogen present
• The prefix "halo-" is used when the specific halogen is not known or a general term is needed
• Nomenclature follows the order: prefix (including halogens), parent chain (longest continuous carbon chain), suffix (based on functional group), and position of substituents
• For multiple halogens of the same type, prefixes like di-, tri-, tetra-, etc. are used (dichloromethane)
• When different halogens are present, they are listed in alphabetical order (bromochloromethane)

Physical Properties

• Organohalides are typically colorless liquids or solids at room temperature, with a few exceptions (iodoform is a yellow solid)
• Generally have higher boiling points and melting points compared to their parent hydrocarbons due to increased molecular mass and intermolecular forces
  • Boiling point increases with the size of the halogen atom: RF < RCl < RBr < RI
• Exhibit low solubility in water but are soluble in organic solvents (hexane, diethyl ether)
  • Solubility decreases with increasing size of the halogen atom
• Have characteristic odors that can be pleasant (chloroform) or pungent (methyl iodide)
• Density increases with the size of the halogen atom, often greater than water (chloroform density = 1.49 g/mL)
• Refractive indices are higher than those of hydrocarbons due to the presence of the polarizable halogen atom
• Dipole moments depend on the polarity of the C-X bond and the molecular geometry (methyl chloride dipole moment = 1.87 D)

Synthesis Methods

• Halogenation of alkanes: Direct reaction of an alkane with a halogen (Cl2 or Br2) under free radical conditions
  • Requires heat or UV light to initiate the reaction
  • Selectivity can be controlled by varying the reaction conditions (temperature, halogen ratio)
• Addition of hydrogen halides to alkenes: Electrophilic addition of HX (X = Cl, Br, I) to the double bond of an alkene
  • Follows Markovnikov's rule, with the halogen attaching to the more substituted carbon
  • Anti-Markovnikov addition can be achieved using peroxide initiators or via hydroboration-halogenation
• Halogenation of alcohols: Replacement of the hydroxyl group (-OH) with a halogen using reagents like thionyl chloride (SOCl2) or phosphorus tribromide (PBr3)
  • Follows an SN2 mechanism with inversion of stereochemistry
• Halogen exchange reactions: Conversion of one organohalide to another by exchanging the halogen atom
  • Finkelstein reaction: Substitution of an alkyl chloride or bromide with an alkyl iodide using sodium iodide (NaI) in acetone
• Dihalogenation of alkenes: Addition of X2 (X = Cl, Br) to the double bond of an alkene, resulting in a vicinal dihalide
  • Stereochemistry depends on the reaction conditions (anti-addition in chloroform, syn-addition in water)

Reactions of Organohalides

• Nucleophilic substitution reactions: Replacement of the halogen with another nucleophile (Nu-)
  • SN2 reaction: Concerted backside attack by the nucleophile, leading to inversion of stereochemistry
    • Favored by primary alkyl halides, strong nucleophiles, and polar aprotic solvents
  • SN1 reaction: Stepwise mechanism involving the formation of a carbocation intermediate
    • Favored by tertiary alkyl halides, weak nucleophiles, and polar protic solvents
• Elimination reactions: Removal of the halogen and an adjacent hydrogen to form an alkene
  • E2 reaction: Concerted anti-periplanar elimination, resulting in the formation of the more stable alkene
    • Favored by strong bases, high temperatures, and bulky bases
  • E1 reaction: Stepwise elimination via a carbocation intermediate, leading to a mixture of alkene isomers
    • Favored by tertiary alkyl halides, weak bases, and polar protic solvents
• Grignard reactions: Formation of a carbon-magnesium bond by reacting an organohalide with magnesium metal in anhydrous ether
  • Grignard reagents (RMgX) are versatile nucleophiles used in the synthesis of alcohols, carboxylic acids, and ketones
• Reduction reactions: Replacement of the halogen with a hydrogen atom using reducing agents like lithium aluminum hydride (LiAlH4) or hydrogen gas with a metal catalyst (H2/Pd)
• Coupling reactions: Formation of new carbon-carbon bonds by coupling two organohalides or an organohalide with another organometallic reagent
  • Examples include Ullmann coupling, Suzuki coupling, and Sonogashira coupling

Mechanisms and Stereochemistry

• SN2 mechanism: Concerted backside attack by the nucleophile, leading to inversion of stereochemistry (Walden inversion)
  • Rate-determining step involves the formation of a pentacoordinate transition state
  • Reaction rate depends on the concentration of both the organohalide and the nucleophile (second-order kinetics)
• SN1 mechanism: Stepwise mechanism involving the formation of a planar carbocation intermediate
  • Rate-determining step is the dissociation of the C-X bond to form the carbocation
  • Reaction rate depends only on the concentration of the organohalide (first-order kinetics)
  • Carbocation can undergo racemization or rearrangement, leading to a mixture of stereoisomers
• E2 mechanism: Concerted anti-periplanar elimination, resulting in the formation of the more stable alkene
  • Requires the C-H and C-X bonds to be in an anti-periplanar orientation (dihedral angle of 180°)
  • Stereochemistry of the alkene depends on the relative stability of the possible isomers (Zaitsev's rule)
• E1 mechanism: Stepwise elimination via a planar carbocation intermediate
  • Carbocation can undergo rearrangement or loss of a proton from multiple positions, leading to a mixture of alkene isomers
• Neighboring group participation: Intramolecular nucleophilic assistance by a nearby heteroatom (oxygen or nitrogen) during substitution reactions
  • Leads to the formation of a cyclic onium ion intermediate and retention of stereochemistry

Applications in Industry and Research

• Organohalides are widely used as solvents in various industrial processes (dichloromethane, chloroform)
• Serve as important intermediates in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals
  • Examples include the synthesis of antibiotics (chloramphenicol), anesthetics (halothane), and pesticides (DDT)
• Used in the production of polymers and plastics (vinyl chloride for PVC, tetrafluoroethylene for Teflon)
• Employed as refrigerants and propellants in air conditioning and aerosol systems (chlorofluorocarbons, CFCs)
  • However, the use of CFCs has been phased out due to their negative impact on the ozone layer
• Organohalides with specific properties are used in fire extinguishers (bromochlorodifluoromethane, Halon 1211)
• In research, organohalides are utilized as precursors for the synthesis of organometallic reagents (Grignard reagents, organolithium compounds)
• Serve as substrates for studying reaction mechanisms and developing new synthetic methodologies
• Radioactive organohalides (18F-labeled compounds) are employed in positron emission tomography (PET) imaging for medical diagnostics

Environmental Impact and Safety

• Many organohalides are toxic and can have adverse effects on human health and the environment
  • Exposure can occur through inhalation, ingestion, or skin contact
  • Chronic exposure may lead to liver and kidney damage, neurological disorders, and cancer
• Chlorofluorocarbons (CFCs) have been linked to the depletion of the ozone layer in the upper atmosphere
  • Montreal Protocol (1987) aimed to phase out the production and consumption of CFCs and other ozone-depleting substances
• Certain organohalides are persistent organic pollutants (POPs) that can bioaccumulate in the food chain
  • Examples include polychlorinated biphenyls (PCBs) and dichlorodiphenyltrichloroethane (DDT)
  • Stockholm Convention (2001) seeks to eliminate or restrict the production and use of POPs
• Proper handling, storage, and disposal of organohalides are crucial to minimize their environmental impact
  • Use of personal protective equipment (gloves, lab coats, fume hoods) is essential when working with these compounds
  • Waste should be collected and disposed of according to local regulations and guidelines
• Research efforts are focused on developing safer and more environmentally friendly alternatives to harmful organohalides
  • Examples include the use of hydrofluorocarbons (HFCs) as refrigerants and the development of biodegradable polymers