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Methyl propyl bromide reacts with and gives whereas on reaction with it gives The mechanism followed in these reactions and the products and respectively are:
(a)
iso-butyl ethyl ether;tert-butyl ethyl ether
(b)
tert-butyl ethyl ether; butyl ethyl ether
(c)
butyl ethyl ether; iso-butyl ethyl ether
(d)
tert-butyl ethyl ether; iso-butyl ethyl ether

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Important Questions on Halogen Derivatives
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In the reaction

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(1)
(2)
(3)
is

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The major product of the following reaction is:

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The increasing order of reactivity of the following compounds towards reaction with alkyl halides directly is:

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For the following compounds the correct statement(s) with respect to nucleophilic substitution reactions is(are)

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This reaction will be the fastest in

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The reagent required for the following two step transformation are

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CH3Cl, CH3CH2Cl, (CH3)2CHCl and (CH3)3CCl is :

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(I)

(II)

(III)

(IV)


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Assertion : Vinyl halides do not undergo nucleophilic substitution easily.
Reason : Even though the intermediate carbocation is stabilized by loosely held electrons, the cleavage is difficult because of the strong bonding.

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