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Which of the following structures are superimposable (identical) :
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Both in (I) & (III) configuration at lower chiral carbon is 'R' and upper chiral carbon is 'S'.
If optical rotation is produced by is + 36o then that is produced by
Rotation of the compound in question is zero because it is a meso compound.
The major product (ester) of the following reaction is
The most stable conformation of 3-fluorobutan-2-ol is :
(Stable due to intramolecular H bonding)
Arrange in decreasing order of e-density in Benzene ring-
Electron donating ability of group order :
-NH2 > -N(CH3)2 > - NH - CHO > -NH2
A Natural Drug was having [a] = 40.3º in polarimeter experiment in clockwise direction what can be the structure of this drug.
is optically active compound so it rotate the plane of ppl.
Acetaldehyde and acetylene can not be distinguished by :
Lucas reagent can not be used to distinguished Acetaldehyde and acetylene.
Which is the most stable resonating structure.
Negative charge on more electronegative atom is more stable.
In which delocalisation of positive charge is possible
In all other cases positive charge is not in conjugation.
Which of the following pairs of structures do not represent resonating structures ?
Structures given in option(A) are tautomers.
Correct (-)
Wrong (-)
Skipped (-)