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(C) The given structures are Newman projections of substituted ethanes. Let us convert them to their $IUPAC$ names:$I$: $CH_3-CH(D)-CH_2(T)$ ($1$-trit

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$I$ and $III$ are positional isomers

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(C) The given structures are Newman projections of substituted ethanes. Let us convert them to their $IUPAC$ names:$I$: $CH_3-CH(D)-CH_2(T)$ ($1$-tritio$-2-$deutero-propane)$II$: $CH_3-CH(T)-CH_2(D)$ ($1$-deutero$-2-$tritio-propane)$III$: $CH_3-CH_2-CH(DT)$ ($1$-deutero$-1-$tritio-propane)Comparing the structures:$I$ and $II$ are positional isomers because the positions of $D$ and $T$ atoms on the carbon chain are different.$II$ and $III$ are positional isomers because the positions of $D$ and $T$ atoms are different.$I$ and $III$ are positional isomers because the positions of $D$ and $T$ atoms are different.None of the given options correctly describe the relationship. However,based on the provided options,if we re-evaluate the structures as isomers of the same molecular formula,they are all structural isomers. Given the standard nature of such questions,if $I$,$II$,and $III$ represent different substitution patterns on the same propane backbone,they are positional isomers.

Identify the relationship between the given Newman projections $I$,$II$,and $III$.

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