Draw the structure of major monohalo product in each of the following reactions: i) ii)
Give reasons:
The presence of nitro group (–NO2) at o/p positions increases the reactivity of haloarenes towards nucleophilic substitution reactions.
Which alkyl halide from the following pair is chiral and undergoes faster SN2 reaction?
Write the IUPAC name of
Out of SN1 and SN2, which reaction occurs with
(a) Inversion of configuration
(b) Racemisation
Which would undergo SN2 reaction faster in the following pair and why?
n-Butyl bromide has higher boiling point than t-butyl bromide.
Racemic mixture is optically inactive.