Draw the structure of the isomers of c6h11br that contains a 5-membered ring and is least reactive in an sn1 reaction.

We have to know the structure of the isomer of C₆H₁₁Br which contains 5-membered ring and is least reactive in an SN¹ reaction.

The structure is: isomer (a) shown in figure where methyl group and Br atom connected to the adjacent carbons in the ring.

There are four isomers possible with molecular formula C₆H₁₁Br. Those are shown in figure as (a), (b), (c), (d).

SN¹ reaction takes place through carbocation  intermediate formation. If carbocation is more stable, SN¹ reaction will be more faster and if carbocation is not stable, SN¹ reaction will be slower.

The stability of carbocation depends on number of α-H atoms. If the number of α-H atom is more, hyperconjugation in the carbocation will be more; as a consequence, SN¹ reaction rate will be faster.

On the other hand, if the number of α-H atom is less, hyperconjugation in the carbocation will be less; as a consequence, SN¹ reaction rate will be slow.

The carbocation of isomer (a) contains  α-H atom= 3, all other isomers contain minimum 4 α-H atoms.

a is the answer

explanation:

which statement about trans-fatty acids is false?

a. the conversion of cis-fatty acids to trans-fatty acids is inhibited by the presence of antioxidants.

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