haloalkanes and haloarenes

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classifications of halides alkyl - R-x allyl - X - C - C = C benzyl - X - C -Ar aryl - X - Ar ( c = c place ) vinyl - X - c = c
nature of c-x bond * x is more electronegative than carbon * size of atom and bond length increases from F - I * BL is inversely to bond enthalpy *dipole moment decreases from F - I
MOP of haloalkanes 1. from alcohols 2. from hydrocarbons 3. from alkenes
from alcohols
from hydrocarbons - from alkanes free radical halogenation CH3 - CH2 - CH2 -CH3 + Cl2 / UV Light or heat -----> CH3 - CH2 - CH2 - CH2 - Cl + CH3 - CH2 - CH (Cl ) - CH3
from alkenes 1 ) Addition of hydrogen halide > C = C < + HX ----> >C H - X C <
from alkenes 2 ) addition of halogen CH2 = CH2 + Br2 ----CCl4 ---> BrCH2-CH2Br
from hydrocarbons FINKELSTEIN REACTION
from hydrocarbons SWARTS REACTION
MOP of haloarenes 1. from hydrocarbons by electrophilic substitution 2 . from amines
from hydrocarbons by electrophilic substitution O and p can seperated due to difference in mp fluoro compound is not created due to high reactivity of fluorine
from amines SANDMEYER'S REACTION Iodine does not require presence or cuprous halide, it'S simply formed by shaking with diazonium salt with KI
WURTZ REACTION 2RX + 2Na ----> RR + 2NaX
HALOGENATION
NITRATION
SULPHONATION
FRIEDEL-CRAFTS REACTION
WURTZ FITTIG REACTION
FITTIG REACTION
DDT
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