(I) m-nitrobromobenzene (II) 2,4,6-trinitrobromobenzene
(III) p-nitrobromobenzene (IV) 2,4-dinitrobromobenzene
The decreasing order of reactivity for given compounds towards OH− ions is:
A
I > II > III > IV
No worries! We‘ve got your back. Try BYJU‘S free classes today!
B
II > IV > III > I
Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses
C
IV > II > III > I
No worries! We‘ve got your back. Try BYJU‘S free classes today!
D
II > IV > I > III
No worries! We‘ve got your back. Try BYJU‘S free classes today!
Open in App
Solution
The correct option is B II > IV > III > I Greater the number of nitro group at ortho and para position to −Br group, greater is the reactivity towards OH− ions due to stabilising of intermediate carbanion. (II) has three nitro groups and is most reactive. (I) has nitro group at meta position is the least reactive.