A hydrocarbon with molecular formula C_5H_12on mono chlorination in presence of light gives four compounds A,B,C,D. A is optically inactive and dehydrohalgenation gives E( major) which on ozonolysis gives acetone and acetaldehyde. B is optically active gives on dehydrohalogenation E also gives E as the major product. Further C is optically active while D is optically inactive. Allcompounds A,B,C,D on reduction give 2-methyl butane.Which of the following is the correct structure of A

A hydrocarbon with molecular formula C_5H_12on mono chlorination in pr

1.	A hydrocarbon with molecular formula C_5H_12on mono chlorination in presence of light gives four compounds A,B,C,D. A is optically inactive and dehydrohalgenation gives E( major) which on ozonolysis gives acetone and acetaldehyde. B is optically active gives on dehydrohalogenation E also gives E as the major product. Further C is optically active while D is optically inactive. Allcompounds A,B,C,D on reduction give 2-methyl butane.Which of the following is the correct structure of A
Answer» `ClCH_2CH(CH_3)CH_2CH_3` `(CH_3)_2C(CL)CH_2CH_3` `(CH_3)_2CHCH(Cl)CH_3` `(CH_3)_2CHCH_2CH_2Cl` SOLUTION :