What is obtained when acetaldehyde is heated with ammoniacal silver nitrate?
- A$CH_3OH$
- BSilver acetate
- C$HCHO$
- DSilver mirror
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The major product of the following reaction is
The major product $(P)$ in the following reaction is $:$
Which of the following carbonyl compounds forms the most stable hydrate when $H_2O$ is added across the $C=O$ group?
Which of these reagents would accomplish the following reduction?
$NC-CH_2-CO-CH_2-CH=CH_2 \to NC-CH_2-CH(OH)-CH_2-CH=CH_2$
$NC-CH_2-CO-CH_2-CH=CH_2 \to NC-CH_2-CH(OH)-CH_2-CH=CH_2$
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View SolutionCompound $(X)$ with molecular formula $C_4H_8O$ reacts with $2,4-DNP$ to form a derivative and gives a negative haloform test. The compound $(X)$ is:
Medium
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