An organic compound 'X' with a molecular formula `C_(4)H_(8)O_(2)` when reacts with excess of methyl magnesium chloride following by acidification gives an alcohol 'Y' only.when this alcohol 'Y' is oxidized with `NaOCl` followed by acidification acidic acid is formed.here the compound 'X' is

An ester 'A' (C_(4)H_(8)O_(2)) on treatment with excess methyl magnesium chloride followed on acidification gives an alcohol 'B' as the sole organic product. Alochol 'B' as the organic product. Alcohol 'B' on oxidation with NaOCl followed by acidification gives acetic acid. Deduce structure of A and B. Show the reactions involved.

A halogen compound 'A' on hydrolyses with dilute alkali followed by acidification gives acetic acid. The compound X is:

An organic compound of molecular formula C_4H_10O does not react with sodium. With excess of HI, it gives only one type of alkyl halide. The compound is

An optically active compound 'X' has molecular formula C_(4)H_(8)O_(3) . It evolves CO_(2) with NaHCO_(3) . 'X' reacts with LiAIH_(4) to give an achiral compound 'X' is:

How many isomer of C_(4)H_(8)O when reacts with CH_(3)MgBr followed by acidification to give 2^(@) alcohol (only consider carbonyl isomers) ? (including stereoisomer)

A compound [A] has the formula C_(4)H_(8)O_(2) . When reacted with a Grignard reagent, CH_(3)MgBr , it takes up two molecules of it and upon acidification gives an alcohol [B]. The alcohol on reacting with Lucas reagent gives white coludiness on standing for sometime. When the alochol is oxidised, a compound [C] is produced with a pleasant smell. It neither reacts with Tollen's reagent, nor with Fehling's reagent. The alcohol [B] is

A compound [A] has the formula C_(4)H_(8)O_(2) . When reacted with a Grignard reagent, CH_(3)MgBr , it takes up two molecules of it and upon acidification gives an alcohol [B]. The alcohol on reacting with Lucas reagent gives white coludiness on standing for sometime. When the alochol is oxidised, a compound [C] is produced with a pleasant smell. It neither reacts with Tollen's reagent, nor with Fehling's reagent. The compound [A] is