For the organic compound CH_3-CH_2-CH_2-CH_2- | vedclass

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(B) carbon atom is chiral if it is bonded to four different groups.The given compound is $n$-heptane: $CH_3-CH_2-CH_2-CH_2-CH_2-CH_2-CH_3$.If we subst

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(B) carbon atom is chiral if it is bonded to four different groups.The given compound is $n$-heptane: $CH_3-CH_2-CH_2-CH_2-CH_2-CH_2-CH_3$.If we substitute a hydrogen atom on the $C-3$ carbon with a group $X$ (where $X 
eq H, CH_3, CH_2CH_3, CH_2CH_2CH_2CH_3$),the carbon becomes a chiral center.The structure becomes $CH_3-CH_2-C^*(H)(X)-CH_2-CH_2-CH_2-CH_3$.Similarly,substituting at $C-4$ would also create a chiral center,but $C-3$ is a valid option provided in the choices.

For the organic compound $CH_3-CH_2-CH_2-CH_2-CH_2-CH_2-CH_3$,at which carbon atom should a substitution occur to make the compound chiral?

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