Compound A and compound B are constitutional isomers with molecular formula C3H7Cl. When compound A is treated with sodium methoxide, a substitution reaction predominates. When compound B is treated with sodium methoxide, an elimination reaction predominates. Required:
Propose structures A and B.

Compound A and compound B are constitutional isomers with molecular formula C3H7Cl.

When compound A is treated with sodium methoxide, a substitution reaction predominates. When compound B is treated with sodium methoxide, an elimination reaction predominates.

Explanation:

Constitutional isomers are the one which differs in the structural formula.

When compound A is treated with sodium methoxide, a substitution reaction predominates.

That means sodium methoxide is a strong base and a strong nucleophile.

But when it reacts with primary alkyl halides it forms a substitution product and when it reacts with secondary alkyl halide it forms mostly elimination product.

The reaction and the structures of A and B are shown below:

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explanation:

d.) the average kinetic energy of the gas particles is greater in container b because its particles move faster.