02:58
Arrangement of .. when attached to benzyl or an unsaturated group in increasing
01:56
The reaction tert butyl bromide undergoes hydrolysis to produce tert butyl alcohol
01:42
Due to the presence of an unpaired electron, free radicals are
05:31
The decreasing order of nucleophilicity among the nucleophiles is
06:16
The decreasing order of the rate of the above reaction with nucleophiles A to D is
03:45
The increasing order of stability of the following free radicals is
05:16
The electrophile E+ attacks the benzene ring to generate the intermediate
05:21
Arrange the carbocations, in order of their decreasing stability
02:59
The order of stability of the following carbocations is
06:31
The increasing order of the boiling points for the following compounds i
03:24
Which of the following compounds will show highest dipole moment?
05:55
Which of the following compounds will form significant amount of meta product
04:13
Which of the following molecules is least resonance stabilized?
05:39
The increasing order of nitration of the following compound is
03:49
Among the following four aromatic compounds, which one will have the lowest melting point?
03:47
The increasing order of the pKa values of the following compounds is
05:08
The decreasing order of ease of alkaline hydrolysis for the following esters is
03:03
Which amongst the following is the strongest acid?
04:08
The increasing order of the reactivity of the following compounds towards electrophilic
07:15
The increasing order of basicity for the following intermediates is (from weak to strong)
03:52
The correct order of stability for the following alkoxides is
04:44
Which of the following compounds will form the precipitate with aq. AgNO3 solution most rapidly?
04:38
The major product of the following reaction is
02:10
Among the following species the resonance stabilized carbocations are
06:02
The correct order of nucleophilicity is
03:30
Which of the following carbocations is most stable?
05:39
Arrange the following carbocations in decreasing order of stability
02:35
Racemic mixture is formed by mixing two
03:10
A similarity between optical and geometrical isomerism is that
03:56
Which of the following does not show geometrical isomerism?
01:45
The IUPAC name of the compound shown below is
02:32
Which of the following molecules is expected to rotate the plane polarized light?
03:06
The absolute configuration of but-1,4-dioic acid
03:00
The alkene that exhibits geometrical isomerism is
02:56
The number of stereoisomerism possible for a compound of the molecular formula CH3-CH=CH-CH(OH)-Me
01:23
The IUPAC name of neo-pentane is
03:09
Out of the following, the alkene that exhibits optical isomerism is
04:46
Identify the compound that exhibits tautomerism
04:33
How many chiral compounds are possible on monochlorination of 2-methyl butane?
03:39
The number of structural isomers for C6H14 is
02:12
Which of the following pairs of compounds are positional isomers?
04:14
Which of the following compounds will exhibit geometrical isomerism?
03:23
The absolute configuration of
04:35
3 methylpent-2-ene on reaction with HBr in presence of peroxide forms an addition product.
02:21
What is the IUPAC name of the following compound?
03:49
The IUPAC name of the following compound is
02:14
The IUPAC name of the following compound is:
03:16
Among the following compounds, geometrical isomerism is exhibited by
02:11
The IUPAC name of the following compound is
03:39
The IUPAC name for the following compound is
04:38
Compounds with molecule formula C3H6O can show
05:19
The correct pairs of the ambidentate nucleophiles is/are
02:14
Mesityl oxide is a common name of
04:32
Which one of the following pairs of isomers is an example of metamerism?
06:01
Experimentally reducing a functional group can not be done by which one of the following reagents?
04:20
Which one among the following resonating structures is not correct?
04:12
Which one of the following compounds des not exhibit resonance?
06:32
Which one of the following molecules does not show stereo isomerism?
05:56
Choose the correct name for compound given below
04:55
The number of stereoisomers possible for 1,2-dimethyl cyclopropane
X
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