7.43 (f) 2,4-Dimethyl-3-pentanot (surruric acid, for e Choose the compound of molecular formula C,H₁,Br that gives each alkene shown as the exclusive product of E2 elimination. (a) (b) O -CH₂ (d) + od bromides both of which yield the indicated

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7.43. A through C

**7.43** Choose the compound of molecular formula C\(_7\)H\(_13\)Br that gives each alkene shown as the *exclusive* product of E2 elimination.

The image shows a question from a chemistry textbook along with six structural diagrams of various cyclic and acyclic alkenes. These are labeled (a) to (f):

- **(a)** Cyclohexene
- **(b)** Cyclohexene with a double bond connecting two adjacent carbon atoms
- **(c)** Methylcyclopentene with a methyl group attached
- **(d)** Cyclopentene with a propyl group attached
- **(e)** Ethylcyclobutene
- **(f)** Trimethylcyclopropene

The task is to identify which of these alkenes can be formed exclusively from a compound with the molecular formula C\(_7\)H\(_13\)Br through an E2 elimination reaction.
Transcribed Image Text:**7.43** Choose the compound of molecular formula C\(_7\)H\(_13\)Br that gives each alkene shown as the *exclusive* product of E2 elimination. The image shows a question from a chemistry textbook along with six structural diagrams of various cyclic and acyclic alkenes. These are labeled (a) to (f): - **(a)** Cyclohexene - **(b)** Cyclohexene with a double bond connecting two adjacent carbon atoms - **(c)** Methylcyclopentene with a methyl group attached - **(d)** Cyclopentene with a propyl group attached - **(e)** Ethylcyclobutene - **(f)** Trimethylcyclopropene The task is to identify which of these alkenes can be formed exclusively from a compound with the molecular formula C\(_7\)H\(_13\)Br through an E2 elimination reaction.
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