An organic compound A has molecular formula `C_8H_16O_2`. It gets hydrolysed with dil. `H_2SO_4` and gives a carboxylic acid B and an alcohol C. Oxidation of C with chronic acid also produced B. C on dehydration gives but-1-ene. Write equations for the reactions involved.

An organic compound A has the molecular formula C_(8)H_(16)O_(2) . It gets hydrolysed with dilute sulphuric acid and gives a carboxylic acid B and an alcohol C. Oxidation of C with chromic acid also produced B, C on. dehydration reaction gives but -l-ene. Write equations for the reactions involved.

A compound Z with molecular formula C_3H_9N reacts with C_6H_5SO_2Cl to give a solid, insoluble in alkali. Identify Z.

An organic compound ‘A’ having molecular formula C_4H_8 on treatment with dil. H_2SO_4 gives B. B on treatment with conc. HCl and anhydrous ZnCl_2 gives secondary halide C. Write all the reactions and identify A, B and C.

An acid having molecular formula C_3H_5O_2Br is optically active. What is its structure ?

An acid having molecular formula C_3H_5O_2Br is optically active. What is its structure ?

An organic compound A with molecular formula C_8H_8O gives positive DNP and iodoform tests. It does not reduce Tollen’s or Fehling’s reagent and does not decolourise bromine water also. On oxidation with chromic acid (H_2CrO_4) , it gives a carboxy acid (B) with molecular formula C_7H_6O_2 . Deduce the structure of A and B.

An organic compound C_8H_18 on monochlorination gives a single monochloride. Write the structure of the hydrocarbon.

An optically active compound having molecular formula C_7H_15Br reacts with KOH to give a racemic mixture of products. Write the mechanism involved for this reaction.

An alkali metal A gives a compound B on reacting with water. The compound B gives a soluble compound C on treatment with aluminium oxide. Identify A,B and C and give the reactions involved.