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The correct IUPAC name of following compound is
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(2- hydroxybutyl) group is substituent.
A hydrocarbon (P) on ozonolysis in presence of zinc gives only one dicarbonyl compound, which gives both Tollen’s and iodoform test. Identify the structure of (P).
Consider the true/false of the following statements:
S1: The most stable resonating structure of p-nitrophenol (not having aromatic ring) is
S2 : In all C–O bonds are of equal length.
S3 : CH3COONa is more resonance stabilised than the protonated acid CH3COOH.
S4 : Benzene ring is more electron dense in phenol than phenoxide.
S1 : Most stable resonating structure is
group has greater +m effect, so it makes phenoxide ion more electron dense.
Choose the strongest base among the following :
Only in (D) the l.p of N atom is not involved in resonance with benzene ring.
A hydrocarbon ‘X’ C7H10 is catalytically hydrogenated to C7H14 ‘Y’. 'Y' gives six monochloro products after photochemical chlorination. The structure of 'X' is -
C7H10 DU = 3
six monochloro products
The feasible reaction is :
Salicylic acid is more acidic than p-hydroxy benzoic acid.
The incorrect information about the given reaction is :
The compound (I) does not racemise during enolisation, because the carbon atom with α-H is not asysmmetric carbon atom.
For the given reaction the correct reactivity order of H-atoms is :
Reactivity depends upon stability of free radicals generated at y,zx and w respectively.
In the given sequence of reactions which of the following is the correct structure of compound A.
Which of the following is not correctly ordered for resonance stability
Follow the rules for stability of resonating structures (structure with more number of p-bonds is more stable).
Correct (-)
Wrong (-)
Skipped (-)