A compound A on oxidation gives acetaldehyde, | vedclass

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(A) The compound $A$ is a primary alcohol $(CH_3CH_2OH)$.Step $1$: Oxidation of primary alcohol $CH_3CH_2OH$ gives acetaldehyde $(CH_3CHO)$.Step $2$:

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Primary alcohol

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(A) The compound $A$ is a primary alcohol $(CH_3CH_2OH)$.Step $1$: Oxidation of primary alcohol $CH_3CH_2OH$ gives acetaldehyde $(CH_3CHO)$.Step $2$: Further oxidation of $CH_3CHO$ gives acetic acid $(CH_3COOH)$.Step $3$: Acetaldehyde $(CH_3CHO)$ reacts with ammoniacal $AgNO_3$ (Tollens' reagent) to produce a silver mirror,which is a characteristic test for aldehydes.Therefore,$A$ is a primary alcohol.

$A$ compound $A$ on oxidation gives acetaldehyde,and further oxidation gives an acid. After the first oxidation,the product reacts with ammoniacal $AgNO_3$ to produce a silver mirror. Compound $A$ is likely to be:

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