The following organic compounds cannot exist. Why? a. 2 -chloro-2-butyne b. 2 -methyl-2-propanone c. 1,1 -dimethylbenzene d. 2 -pentanal e. 3 -hexanoic acid f. 5,5 -dibromo- 1 -cyclobutanol

Consider the structures of each compound and identify any issues preventing their existence. a. 2-chloro-2-butyne: This compound is supposed to be an alkyne with 4 carbons and a chlorine on the second carbon. Butynes only have triple bonds between the two internal carbons, e.g., between carbons 2 and 3 for butynes. A 2-chloro-2-butyne would require a triple bond between the first and second carbon, which is not possible because carbon1 has 3 bonds already. b. 2-methyl-2-propanone: This compound would have a methyl group connected to the carbonyl carbon of propanone. However, the carbonyl carbon in a ketone like propanone already has 3 bonds, making it impossible to bond to another methyl group. c. 1,1-dimethylbenzene: This compound has two methyl groups connected to carbon 1 on the benzene ring. However, carbons in the benzene ring can only have two bonds each, making it impossible for carbon 1 to bond to two methyl groups. d. 2-pentanal: This compound is supposed to be an aldehyde with a total of 5 carbons. But aldehydes have a carbonyl group at the end of the carbon chain, not within or at any other position. Hence, the name "2-pentanal" is incorrect, and the compound cannot exist. e. 3-hexanoic acid: This compound is supposed to be a carboxylic acid with 6 carbons and a carboxyl group on the third carbon. Carboxylic acids have a carboxyl group at the end of the carbon chain, not within or at any other position. So, 3-hexanoic acid cannot exist. f. 5,5-dibromo-1-cyclobutanol: The compound is supposed to be a cyclobutanol compound with a hydroxyl group on the first carbon and two bromine atoms on the fifth carbon. However, cyclobutanol can only have 4 carbons in its ring structure, and thus there cannot be a fifth carbon for the bromine atoms.