Short Answer Type

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Draw the structure of major monohalo product in each of the following reactions: 
i) 


ii) 

 


i) 


(ii) Addition in presence of peroxide yields product according to the anti-Markovnikov rule of addition. Anti Markovnikov rule says - in an addition reaction of a generic electrophile HX to an alkene or alkyne, the hydrogen atom of HX becomes bonded to the carbon atom that had the least number of hydrogen atoms in the starting alkene or alkyne. 

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Out of SN1 and SN2, which reaction occurs with

(a) Inversion of configuration

(b) Racemisation 

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Write the IUPAC name of


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Give reasons:

The presence of nitro group (–NO2) at o/p positions increases the reactivity of haloarenes towards nucleophilic substitution reactions.

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Which would undergo SN2 reaction faster in the following pair and why?

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Give reasons:

Racemic mixture is optically inactive.

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Long Answer Type

Give the laboratory preparation of the Iodoform and its mechanism?
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Short Answer Type

Give reasons:

n-Butyl bromide has higher boiling point than t-butyl bromide.

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Which alkyl halide from the following pair is chiral and undergoes faster SN2 reaction?

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Write the resonance structure of chlorobenzene. Why is chlorobenzene less reactive than chloromethane towards nucleophiles?
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