Advertisements
Advertisements
Question
Why do alkenes prefer to undergo electrophilic addition reaction while arenes prefer electrophilic substitution reactions? Explain.
Advertisements
Solution
If arenes would undergo electrophilic addition reaction then they would lose their aromaticity which would lead to comparatively less stability. However, alkenes undergo electrophilic addition reaction via carbocation intermediate.
APPEARS IN
RELATED QUESTIONS
Arrange the set of compound in order of their decreasing relative reactivity with an electrophile, E+ Chlorobenzene, 2,4-dinitrochlorobenzene, p-nitrochlorobenzene.
Arrange the set of compound in order of their decreasing relative reactivity with an electrophile, E+ Toluene, p-H3C–C6H4–NO2, p-O2N–C6H4–NO2.
Suggest the name of a Lewis acid other than anhydrous aluminium chloride which can be used during ethylation of benzene.
For an electrophilic substitution reaction, the presence of a halogen atom in the benzene ring:
(i) deactivates the ring by inductive effect
(ii) deactivates the ring by resonance
(iii) increases the charge density at ortho and para position relative to meta position by resonance
(iv) directs the incoming electrophile to meta position by increasing the charge density relative to ortho and para position.
In an electrophilic substitution reaction of nitrobenzene, the presence of nitro group:
(i) Deactivates the ring by inductive effect.
(ii) Activates the ring by inductive effect.
(iii) Decreases the charge density at ortho and para position of the ring relative to meta position by resonance.
(iv) Increases the charge density at meta position relative to the ortho and para positions of the ring by resonance.
Why does presence of a nitro group make the benzene ring less reactive in comparison to the unsubstituted benzene ring. Explain.
Assertion (A): Nitration of benzene with nitric acid requires the use of concentrated sulphuric acid.
Reason (R): The mixture of concentrated sulphuric acid and concentrated nitric acid produces the electrophile, \[\ce{NO^{+}2}\].
Choose an INCORRECT statement about the electrophilic substitution reaction mechanism from the following:
In Friedel-Crafts alkylation of aniline, one gets ______.
Excess of isobutane on reactions with Br2 in presence of light at 125°C gives which one of the following, as the major product?
hydrocarbon (X) major product X is:
Benzene on nitration gives nitrobenzene in presence of HNO3 and H2SO4 mixture, where ______.
Which of the following would not give 2-phenylbutane as the major product in a Friedel-Crafts alkylation reaction?
Which one of the following compounds does not decolourise bromine water?
