Arrange the following alkyl halides in decreasing order of their reactivity towards reaction:
(i) CHCHCHCHBr
(ii) (CH)CBr
(iii) CHCHCHBrCH
(iv) CHCHCHCHCl
ii > iii > i > iv
i > ii > iii > iv
iv > iii > ii > i
iii > ii > i > iv
Related Questions
Which halogen has the highest electronegativity?
Chlorine
Bromine
Iodine
Fluorine
Which one of the following compound does not react with bromine?
Ethyl amine
Propene
Phenol
Chloroform
1, 2 Dibromopropane on treatment with ‘x’ moles of followed by treatment with gives a 2-pentyne. The value of ‘x’ is
1
2
3
4
Which of the following reaction(s) can be used for the preparation of alkyl halides?
i)
ii)
iii)
iv)
IV only
III and IV only
I, III and IV only
I and II only
Predict the major product formed when (R)-2-bromobutane is treated with potassium tert-butoxide in tert-butanol.
butan-2-ol
but-2-ene
but-1-ene
(S)-2-bromobutane
Arrange the following C-X bonds in increasing order of bond enthalpy:
In the following reaction . The product ‘X’ is
Which of the following compounds will undergo an reaction most readily?
(CH)CBr
CHCHBr
(CH)CHBr
CHBr
Following reaction,
is an example of
Elimination reaction
Free radical substitution
Nucleophilic substitution
Electrophilic substitution
In the reaction of 2-chloro-2-methylpropane with water, the rate-determining step involves:
Formation of a carbocation
Attack of the nucleophile
Formation of a transition state
Protonation of the leaving group