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In the reaction
the structure of the product T is :
In the following reaction sequence, the correct structures of E, F and G are
[* implies 13C labelled carbon]In Cannizzaro reaction given below
the slowest step is :
An organic compound ‘A’ on treatment with NH3 gives ‘B’which on heating gives ‘C’, ‘C’ when treated with Br2 in the presence of KOH produces ethylamine. Compound ‘A’ is:
Since, C when heated with Br2 in presence of KOH produces ethylamine, hence it must be propanamide and hence the organic compound (A) will be propanoic acid. The reactions follows.
The order of reactivity of phenyl magnesium bromide(PhMgBr) with the following compounds
The reactivity of the carbonyl group toward the nucleophilic addition reactions depend upon themagnitude of the positive charge on the carbonyl carbon atom (electronic factor) and also on the crowding around the carbonyl carbon atom in the transition state (steric factor). Both these factors predict the following order
(due to steric crowding).
Which one of the following compounds will be most readily dehydrated?
The intermediate is carbocation which is destabilised by C = O group in the first three cases. In(d),α–hydrogen is more acidic which can be removed as water. Moreover, the positive charge on the intermediate carbocation is relatively away from the C = O group.
In a set of reactions, ethylbenzene yield a product D.
Identify D:
Which of the following reagent(s) used for the conversion?
Cannizaro’s reaction is not given by :
Only those aldehydes which do not have α-H atom undergo Cannizaro’s reaction. Hence CH3CHO will not undergo Cannizaro’s reaction as it has 3 α-H atoms.
Calculate number of molecules of Grignard reagent consumed by 1 molecule of following compound.