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.

A hydrocarbon of formulaC4H8 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

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