An organic compound (A) (molecular formula `C_6H_(12)O_2)` was hydrolysed with dil . `H_2SO_4` to give carboxylic acid (B) and an alcohol (C). 'C' gives white turbidity immediately when treated with anhydrous `ZnCl_2` and conc. HCl . The organic compound (A) is

A group C_6H_12O_2 which react with H_2SO_4 and gives carboxylic acid B and alcohol C. C react with ZnCl_2 and give white turbidity readily. Identify the structure of A.

A group C_6H_12O_2 which react with H_2SO_4 and gives carboxylic acid B and alcohol C. C react with ZnCl_2 and give white turbidity readily. Identify the structure of A.

An organic compound (A) (molecular formula, C_4H_8O_2 ) was hydrolysed with dilute H_2SO_4 to give a carboxylic acid (B) and alcohol (C ). Oxidation of (C ) with chromic acid produced (B). Write possible structures of (A), (B) and (C ) and give their IUPAC name. Write the chemical equations involved in the process.

An organic compound (A) (molecular formula C_(8)H_(16)O_(2)) was hydrolysed with dilute sulphuric acid to give a carboxylic acid (B) and an alcohol (C ). Oxidation of (C ) with chromic acid produced (B). (C ) on dehydration gives but-1-ene. Write equations for the reactions involved.

An organic compound (A) (molecular formula C_(8)H_(16)O_(2)) was hydrolysed with dilute sulphuric acid to give a carboxylic acid (B) and an alcohol (C ). Oxidation of (C ) with chromic acid produced (B). (C ) on dehydration gives but-1-ene. Write equations for the reactions involved.

An organic compound (A) (molecular formula C8H16O2) was hydrolysed with dilute sulphuric acid to give a carboxylic acid (B) and an alcohol (C). Oxidation of (C) with chromic acid produced (B). (C) on dehydration gives but-1-ene. Write equations for the reactions involved.