JEE MainChemistryCompounds Containing NitrogenMCQ+4 / −1
The increasing order of basicity of the following compounds is : 

- A(d) < (b) < (a) < (c)
- B(a) < (b) < (c) < (d)
- C(b) < (a) < (c) < (d)
- D(b) < (a) < (d) < (c)
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Correct answer: D
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Basicity depends on availability of the lone pair on nitrogen.
A nitrogen compound is more basic when its lone pair is more available for protonation.
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Key effects to compare:
- Resonance delocalization of the lone pair decreases basicity.
- Electron-donating groups increase basicity.
- Hybridization matters: generally, in terms of basicity contribution from lone-pair availability.
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From the given set, the relative basicity pattern corresponds to:
- (b) = least basic, because the lone pair is most strongly delocalized / least available.
- (a) = more basic than (b), but still less basic than the more donating amine-type structures.
- (d) = more basic than (a), due to greater lone-pair availability.
- (c) = most basic, where the lone pair is most available and/or electron donation is highest.
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Therefore, the increasing order of basicity is:
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Match with options:
- Option A: ❌
- Option B: ❌
- Option C: ❌
- Option D: ✅
Hence, Option D is correct.
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