Free Radical Halogenation
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- 24.98 g
- 32.18 g
- 44.86 g
- 13.48 g
How many structures of F are possible ?
2
5
6
3
- (CH3)3CCH2CH(CH3)CH2Cl
- (CH3)2C(CH2Cl)CH2CH(CH3)2
- (CH3)3CCH2C(Cl)(CH3)2
- (CH2Cl)3CCH2CH(CH2Cl)2
Chlorination of isobutane mainly gives
Isobutyl chloride
tert-butyl chloride
Both a & b
None of the above
- (CH3)3CCH2CH(CH3)CH2Cl
- (CH3)2C(CH2Cl)CH2CH(CH3)2
- (CH3)3CCH2C(Cl)(CH3)2
- (CH2Cl)3CCH2CH(CH2Cl)2
- o-cresol
- p-cresol
- mixture of o-cresol and p-cresol
- benzoic acid
From the options given below, choose the one that helps accomplish the given (above)conversion:
A: allyl bromination of propylbenzene using NBS, hν B: E2 with a stong bulky base
A: allyl bromination of propylbenzene using NBS, hν B: treatment with OH− at 0∘C
A: allyl bromination of propylbenzene using NBS, hν B: treatment with NH3 at 0∘C
None of the above
- o-Cresol
- p-Cresol
- 2, 4-Dihydroxytoluene
- Benzoic acid
- C4H10
- C2H4
- C3H6
- C2H2
Methyl cyclopentane undergoes free radical mono-bromination in the presence of light; the major product is:
(bromomethyl)cyclopentane
1-bromo-2-methylcyclopentane
1-bromo-1-methylcyclopentane
1-bromo-3-methylcyclopentane
When chlorine passed through propene at 400 degree Celsius, the product is:
Vinyl chloride
Allyl chloride
PVC
1, 2-dichloroethane
The product (C) is: