An organic compound A having molecular formula C4H8 on hydration with dilH2SO4 gives B. B on treatment with conc HCL and anhydrousZnCl2 gives C and on treatment with sodium ethoxide gives back A. Identify the compounds A,B and C and write the equations involved. Share with your friends Share 19 Geetha answered this A hydrocarbon of formula C4H8 on hydration with dil sulphuric acid gives B. So A is an alkene with general formula CnH2n and it gives alcohol B. Alcohol Breacts with Anhy ZnCl2 and Con HCl (lucas reagent) to give haloalkane. Which reacts withsodium ethoxide to give an alkene back.CH3CH2CH=CH2 →Hg2+dil H2SO4 CH3CH2CH(OH)-CH3 →anhy ZnCl2Con HCl CH3CH2CH(Cl)-CH3 →C2H5ONa CH3CH2CH(OC2H5)-CH3 + NaCl A B C CH3CH2CH(OC2H5)-CH3 →∆ CH3CH2CH=CH2 + C2H5OHThus A = 1-buteneB= 2 -butanolC =2-chlorobutane 18 View Full Answer