Haloalkanes And Haloarenes Flashcards
Preparation of halo alkanes from alcohols ROH + HCl --ZnCl2-->? ROH+ NaBr--H2SO4-->? ROH--Red Phos./X2-->? ROH+ PCl5-->? ROH+S0Cl2-->?
ROH + HCl --ZnCl2-->RCl + H20 ROH+ NaBr--H2SO4--- >RBr + NaHS04+ H20 ROH--Red Phos./X2-->RX ROH+ PCl5-->RCl + S02+ HCl ROH+S0Cl2-->RCl+S02+HCl
Preparation of halo alkanes from hydrocarbons steps ?
By free radicle Halogenation
CH3CH2CH2CH3–Cl2/UV light–>CH3CH2CH2CH2Cl+ CH3CH2CHClCH3
By electrophilic substitution
By Sandmeyer’s Rection
From Alkenes by addition of hydrogen halide and by addition of halogens.
Finkelstein reaction
RX+NaI–Acetone–>?
RX+NaI–Acetone–>RI+NaX
Swart's Reaction R-Br+ AgF---->? R-Br+HgF2---->? R-Br+CoF3---->? R-Br+SbF3---->?
R-Br+ AgF—->RF
R-Br+HgF2—->RF
R-Br+CoF3—->RF
R-Br+SbF3—->RF
Hunsdiecker Reaction
CH3COOAg+Br2–CCl4–>?
CH3COOAg+Br2–CCl4–>CH3Br+AgBr+CO2
Reactions of Halo alkanes :
Hoffmann Ammonolysis
RBr–NH2–>?
RBr–NH2–>RNH2
Reactions of halo alkanes :
Reaction with cyanides
R-Br–KCN–>?
R-Br–AgCN–>?
R-Br–KCN–>RCN+KBr
R-Br–AgCN–>RNC+AgBr
Nucleophilic Substitution Reaction R-Br--KOH-->? R-Br--KNO2-->? R-Br--AgNO2-->? R-Br--R'COOAg-->?
R-Br–KOH–>ROH+KBr
R-Br–KNO2–>R-ONO+KBr
R-Br–AgNO2–>RNO2+AgBr
R-Br–R’COOAg–>R0C0-R’+ AgBr
Reaction of Haloalkanes :
Elimination Reaction
R-CH2-CH(Br)-R’–alc.K0H–>?
R-CH2-CH(Br)-R’–alc.K0H–>R-CH=CH-R’
Reaction of Haloalkanes :
By reduction
R-Br+H2–N2,573K–>?
R-I+HI–Red Phos, 420K–>?
R-Br+H2–N2,573K–>RH + HBr
R-I+HI–Red Phos, 420K–> RH + I2
Reaction of Haloalkanes :
Wurtz Reaction
RX+ 2Na+ XR–Dry ether–> ?
RX+ 2Na+ XR–Dry ether–> R-R+ 2NaX
Reaction of halo alkanes:
Wurtz Fittig Reaction
RX+ 2Na+ X-R’–dry ether–>?
RX+ 2Na+ X-R’–dry ether–> R-R’ + 2NaX
Rection of Haloalkanes :
Reaction with magnesium
RX+Mg–Dry Ether–>RMgX
RX+Mg–Dry Ether–>RMgX
Reaction of Haloalkanes :
Isomerisation
CH3-CH2-CH2-Cl–573K–> ?
CH3-CH2-CH2-Cl–573K–> CH3-CH(Cl)-CH3
Preparation of Aryl halides:
Sandmeyer’s reaction
C6H5-(N2+)Cl–CuCl/HCl–>?
C6H5-(N2+)Cl- –CuBr/HBr–>?
C6H5-(N2+)Cl–CuCl/HCl–>C6H5-Cl+N2
C6H5-(N2+)Cl- –CuBr/HBr–>C6H5-Br+N2
Preparation of Aryl halide:
By Halogenation of aromatic hydrocarbon
C6H6+Cl2–FeCl3,dark–>?
C6H6+Cl2–FeCl3,dark–>C6H5-Cl+HCl
Preparation of Aryl halide:
By side chain Halogenation
C6H5-CH3+Cl2–383K,sunlight–>?
C6H5-CH3+Cl2–383K,sunlight–>C6H5-CH2Cl
Preparation of Aryl halide:
Gattermann Reaction
C6H5-(N2+)Cl- –Cu,HCl–>?
C6H5-(N2+)Cl- –Cu,HCl–>C6H5-Cl + N2
Preparation of Aryl halide :
By Balz shiemann reaction
C6H5-(N2+)Cl- —->?
C6H5-(N2+)Cl- —->C6H5-F
Preparation of Aryl halide:
By formation of Iodo Benzene
C6H5-(N2+)Cl- –KI–>?
C6H5-(N2+)Cl- –KI–>C6H5-I +N2 +KCl
Preparation of Aryl halide:
From Phenol
C6H5-OH+ PCl3—->?
C6H5-OH+PCl3—-> C6H5-Cl + HCL + POCl3
Reaction of Aryl Halides:
Nucleophilic Substitution Reaction
C6H5-Cl–NaOH,H+–>?
(p-NO2)C6H4-Cl–NaOH,H+–>?
C6H5-Cl–NaOH,H+–>C6H5-OH
(p-NO2)C6H4-Cl–NaOH,H+–>(p-NO2)C6H4-OH
Reaction of Aryl Halide:
Halogenation
C6H5-Cl+ Cl2–anhy. FeCl3–>?
C6H5-Cl+ Cl2–anhy. FeCl3–>(o-Cl)-C6H4-Cl+ (p-Cl)-C6H4-Cl
;para is major here
Reaction of Aryl Halide:
Nitration
C6H5-Cl–HNO3–>?
C6H5-Cl–HNO3–>(o-NO2)C6H4-Cl +(p-NO2)C6H4+ Cl
Reaction of Aryl halides:
Sulphonation
C6H5-Cl–conc H2S04–>?
C6H5-Cl–conc H2S04–>(o-SO3H)-C6H4-Cl + (p-SO3H)C6H4-C
;para one is major
Reaction of Aryl halides :
Ulmann Reaction
C6H5-I+Cu powder—->?
C6H5-I+Cu—->C6H5-C6H5