3 Halogenalkanes Flashcards
(8 cards)
Why can haloalkanes undergo nucelophilic substitution?
the contain a polar C-X bond
As X gets bigger, the bond length increases so the energy required to break than bond decreases
Nucelophilic substitution of haloalkanes with OH-
Forms alcohol and X-
Nucelophilic substitution of haloalkanes with CN-
Forms nitrile and X-
requires ethanolic aqueous KCN
Nucelophiles
contain a lone pair of electrons that is attracted to δ+ regions
Nucleophilic substitution with NH3
Produces an amine and X-
Can react again to form secondary amines
Elimination of haloalkanes
When heated to a high temperature under ethanolic conditions.
OH- nucelophile acts as a base, removing H from molecule to eliminate halide, forming C=C
can only occur in secondary or tertiary haloalkanes
Ozone’s role in the atmosphere
Ozone in the atmosphere absorbs harmful UV radiation
How does ozone depletion occur?
CFCs absorb UV radiation, breaking down C-Cl bond to form Cl. These Cl react with O3 to break it down
O3 + Cl* → *OCl + O2
OCl + O3→ 2O2 + Cl