Which of the following reactions is appropriate for converting acetamide to methanamine?
1. Hoffmann hypobromamide reaction
2. Stephens reaction
3. Gabriels phthalimide synthesis
4. Carbylamine reaction
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CH2=CH-CHO+HCNA(Major),
the compound 'A' is
1. CH2=CH-CH-CH(OH)(CN)
2. CH3-CH(CN)-CHO
3. CH2(CN)-CH2-CHO
4. CH3-C(OH)(CN)-CH3
The slowest step of Cannizarro's reaction is
1. Attack of nucleophilic
2. Hydride shift
3. Formation of anion
4. Transfer of proton
Product,
Product is:-
1.
2.
3.
4.
The structure of the product is:
1. | 2. | ||
3. | 4. |
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Which shows decarboxylation by heating
1.
2.
3.
4.
The major product is
\(\xrightarrow{LiAlH_4}\)
1. | 2. | ||
3. | 4. |