The alkene that will give the same product with HBr in the absence as well as in the presence of peroxide is
2-butene
1-butene
propene
2-methylpropene
Chlorination of benzene in the presence of halogen carrier is an example of
aromatic nucleophilic substitution
aromatic electrophilic substitution
aromatic nucleophilic addition
aromatic electrophilic addition
For preparing an alkane, a saturated solution of sodium or potassium salt of a carboxylic acid is subjected to
hydrolysis
electrolysis
oxidation
hydrogenation
An organic compound with molecular formula C6H12 upon ozonolysis give only acetone as the product. The compound is
2,3-dimethyl-1-butene
3-hexane
2-hexene
2,3-dimethyl-2-butene
An alkene having the molecular formula C9H18 on ozonolysis gives 2, 2-dimethyl propanal and 2-butanone. The alkene is :
2, 2, 2-trimethyl-3-hexene
2, 2, 6-trimethyl-3-hexane
2, 3, 4-trimethyl-2-hexene
2, 2, 4-trimethyl-3-hexene
Observe the following reactions and predict the nature of A and B:
A and B both are
A and B both are
A is and B is
A is and B is
Nitration of aniline in strongly acidic medium, result in the formation of m-nitroaniline also. This is because :
amino group is meta orienting during electrophilic substitution reaction
nitro group goes always to the meta position irrespective of the substituents
nitration of aniline is a nucleophilic substitution reaction in strongly acidic medium
in strongly acidic conditions aniline is present as anilinium ion