Haloalkanes And Haloarenes Flashcards

1
Q
Preparation of halo alkanes  from alcohols 
ROH + HCl --ZnCl2-->?
ROH+ NaBr--H2SO4-->?
ROH--Red Phos./X2-->?
ROH+ PCl5-->?
ROH+S0Cl2-->?
A
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
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2
Q

Preparation of halo alkanes from hydrocarbons steps ?

A

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.

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3
Q

Finkelstein reaction

RX+NaI–Acetone–>?

A

RX+NaI–Acetone–>RI+NaX

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4
Q
Swart's Reaction 
R-Br+ AgF---->?
R-Br+HgF2---->?
R-Br+CoF3---->?
R-Br+SbF3---->?
A

R-Br+ AgF—->RF
R-Br+HgF2—->RF
R-Br+CoF3—->RF
R-Br+SbF3—->RF

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5
Q

Hunsdiecker Reaction

CH3COOAg+Br2–CCl4–>?

A

CH3COOAg+Br2–CCl4–>CH3Br+AgBr+CO2

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6
Q

Reactions of Halo alkanes :
Hoffmann Ammonolysis
RBr–NH2–>?

A

RBr–NH2–>RNH2

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7
Q

Reactions of halo alkanes :
Reaction with cyanides
R-Br–KCN–>?
R-Br–AgCN–>?

A

R-Br–KCN–>RCN+KBr

R-Br–AgCN–>RNC+AgBr

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8
Q
Nucleophilic Substitution Reaction 
R-Br--KOH-->?
R-Br--KNO2-->? 
R-Br--AgNO2-->?
R-Br--R'COOAg-->?
A

R-Br–KOH–>ROH+KBr
R-Br–KNO2–>R-ONO+KBr
R-Br–AgNO2–>RNO2+AgBr
R-Br–R’COOAg–>R0C0-R’+ AgBr

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9
Q

Reaction of Haloalkanes :
Elimination Reaction
R-CH2-CH(Br)-R’–alc.K0H–>?

A

R-CH2-CH(Br)-R’–alc.K0H–>R-CH=CH-R’

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10
Q

Reaction of Haloalkanes :
By reduction
R-Br+H2–N2,573K–>?
R-I+HI–Red Phos, 420K–>?

A

R-Br+H2–N2,573K–>RH + HBr

R-I+HI–Red Phos, 420K–> RH + I2

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11
Q

Reaction of Haloalkanes :
Wurtz Reaction
RX+ 2Na+ XR–Dry ether–> ?

A

RX+ 2Na+ XR–Dry ether–> R-R+ 2NaX

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12
Q

Reaction of halo alkanes:
Wurtz Fittig Reaction
RX+ 2Na+ X-R’–dry ether–>?

A

RX+ 2Na+ X-R’–dry ether–> R-R’ + 2NaX

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13
Q

Rection of Haloalkanes :
Reaction with magnesium
RX+Mg–Dry Ether–>RMgX

A

RX+Mg–Dry Ether–>RMgX

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14
Q

Reaction of Haloalkanes :
Isomerisation
CH3-CH2-CH2-Cl–573K–> ?

A

CH3-CH2-CH2-Cl–573K–> CH3-CH(Cl)-CH3

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15
Q

Preparation of Aryl halides:
Sandmeyer’s reaction
C6H5-(N2+)Cl–CuCl/HCl–>?
C6H5-(N2+)Cl- –CuBr/HBr–>?

A

C6H5-(N2+)Cl–CuCl/HCl–>C6H5-Cl+N2

C6H5-(N2+)Cl- –CuBr/HBr–>C6H5-Br+N2

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16
Q

Preparation of Aryl halide:
By Halogenation of aromatic hydrocarbon
C6H6+Cl2–FeCl3,dark–>?

A

C6H6+Cl2–FeCl3,dark–>C6H5-Cl+HCl

17
Q

Preparation of Aryl halide:
By side chain Halogenation
C6H5-CH3+Cl2–383K,sunlight–>?

A

C6H5-CH3+Cl2–383K,sunlight–>C6H5-CH2Cl

18
Q

Preparation of Aryl halide:
Gattermann Reaction
C6H5-(N2+)Cl- –Cu,HCl–>?

A

C6H5-(N2+)Cl- –Cu,HCl–>C6H5-Cl + N2

19
Q

Preparation of Aryl halide :
By Balz shiemann reaction
C6H5-(N2+)Cl- —->?

A

C6H5-(N2+)Cl- —->C6H5-F

20
Q

Preparation of Aryl halide:
By formation of Iodo Benzene
C6H5-(N2+)Cl- –KI–>?

A

C6H5-(N2+)Cl- –KI–>C6H5-I +N2 +KCl

21
Q

Preparation of Aryl halide:
From Phenol
C6H5-OH+ PCl3—->?

A

C6H5-OH+PCl3—-> C6H5-Cl + HCL + POCl3

22
Q

Reaction of Aryl Halides:
Nucleophilic Substitution Reaction
C6H5-Cl–NaOH,H+–>?
(p-NO2)C6H4-Cl–NaOH,H+–>?

A

C6H5-Cl–NaOH,H+–>C6H5-OH

(p-NO2)C6H4-Cl–NaOH,H+–>(p-NO2)C6H4-OH

23
Q

Reaction of Aryl Halide:
Halogenation
C6H5-Cl+ Cl2–anhy. FeCl3–>?

A

C6H5-Cl+ Cl2–anhy. FeCl3–>(o-Cl)-C6H4-Cl+ (p-Cl)-C6H4-Cl

;para is major here

24
Q

Reaction of Aryl Halide:
Nitration
C6H5-Cl–HNO3–>?

A

C6H5-Cl–HNO3–>(o-NO2)C6H4-Cl +(p-NO2)C6H4+ Cl

25
Q

Reaction of Aryl halides:
Sulphonation
C6H5-Cl–conc H2S04–>?

A

C6H5-Cl–conc H2S04–>(o-SO3H)-C6H4-Cl + (p-SO3H)C6H4-C

;para one is major

26
Q

Reaction of Aryl halides :
Ulmann Reaction
C6H5-I+Cu powder—->?

A

C6H5-I+Cu—->C6H5-C6H5