Which of the following gives two isomers of $3^o$ alcohol,when treated with phenyl magnesium bromide?

An organic compound contains $69.77 \%$ carbon,$11.63 \%$ hydrogen and the rest is oxygen. The molecular mass of the compound is $86$. It does not reduce Tollens' reagent but forms an addition compound with sodium hydrogensulphite and gives a positive iodoform test. On vigorous oxidation,it gives ethanoic acid and propanoic acid. Write the possible structure of the compound.

An organic compound $(A)$ with molecular formula $C_8H_8O$ forms an orange-red precipitate with $2,4-DNP$ reagent and gives a yellow precipitate on heating with iodine in the presence of sodium hydroxide. It neither reduces Tollens' or Fehlings' reagent,nor does it decolourise bromine water or Baeyer's reagent. On drastic oxidation with chromic acid,it gives a carboxylic acid $(B)$ having molecular formula $C_7H_6O_2$. Identify the compounds $(A)$ and $(B)$ and explain the reactions involved.

Benzophenone can be converted into benzene using

Which reagent is used to distinguish between acetaldehyde and acetophenone?

Which one of the following is the major product of the given reaction?