In the reaction
the structure of the product T is :
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Solution
In the following reaction sequence, the correct structures of E, F and G are
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Solution
In Cannizzaro reaction given below
the slowest step is :
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Solution
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:
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Solution
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
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Solution
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?
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Solution
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:
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Solution
Which of the following reagent(s) used for the conversion?
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Solution
Cannizaro’s reaction is not given by :
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Solution
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.
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Solution