Resonance Effect
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Resonance is not exhibited by................…?
Phenol
Aniline
Nitrobenzene
Cyclohexane
Resonance hybrid is more stable than the resonating forms but the energy of the resonance hybrid is:
Does not depend upon the resonating forms
More than resonating forms
Equal to resonating forms
Less than resonating forms
Choose the correct decreasing order of stablity:
- (i)>(ii)>(iii)
- (i)>(iii)>(ii)
- (ii)>(iii)>(i)
- (iii)>(ii)>(i)
- Resonating structures have a real existence
- The actual structure lies between various possible resonating structures
- Resonating structures are useful as they allow us to describe the molecule properties
- None of the mentioned
Which of the following weak acids ionizes to give the strongest conjugate base?
HClO
CH3COOH
HF
HNO2
| CH3−⊕CH−CH3 || CH3−⊕CH−OCH3 ||| CH3−⊕CH−COCH3
I > II > III
II > III > I
III > I > II
II > I > III
The number of lone pairs of electrons on SF4, CF4 and XeF4 are:
2, 0 and 1 lone pairs of electrons respectively
1, 1 and 1 lone pairs of electrons respectively
0, 1 and 2 lone pairs of electrons respectively
1, 0 and 2 lone pairs of electrons respectively
Trihalides are less covalent than pentahalides. Justify
A compound having molecular formula NH2CH2COOH is expected to behave
Only as acid
Neither acid nor base
Both acid and base
Only as base
All bonds in benzene are equal due to
Tautomerism
Inductive effect
Resonance
Isomerism
- Ph−NH2
- Ph−+NH3
- Ph−OH
- Ph−Cl
Among the following, the least stable resonance structure is:
Arrange the following compounds in order of decreasing acidity:
I > II > III > IV
III > I > II > IV
IV > III > I > II
II > IV > I > III